Collection of Czechoslovak Chemical Communications - digital archive 

Crossref Cited-by Linking

• Zhang Jing, She Ping, Xu Qiang, Tian Fengkun, Rao Heng, Qin Jun‐Sheng, Bonin Julien, Robert Marc: Efficient Visible‐Light‐Driven Carbon Dioxide Reduction using a Bioinspired Nickel Molecular Catalyst. ChemSusChem 2024. <https://doi.org/10.1002/cssc.202301892>
• Li Hao‐Yuan, Niu Xiaoying, Yang Xiu‐Long: Photoinduced Generation of Active Intermediates from Unmodified 1,3‐Dicarbonyl Compounds for Organic Transformations. Eur J Org Chem 2024, 27. <https://doi.org/10.1002/ejoc.202400102>
• Yuan Yurong, Faure Clara, Berthelot Mathieu, Belmont Philippe, Brachet Etienne: Harnessing the Potential of Electron Donor–Acceptor Complexes and N-Centered Radicals: Expanding the Frontiers of Isoquinoline Derivative Synthesis. J. Org. Chem. 2024, 89, 3538. <https://doi.org/10.1021/acs.joc.4c00086>
• Morozkov Gleb V., Abel Anton S., Lyssenko Konstantin A., Roznyatovsky Vitaly A., Averin Alexei D., Beletskaya Irina P., Bessmertnykh-Lemeune Alla: Ruthenium(ii) complexes with phosphonate-substituted phenanthroline ligands as reusable photoredox catalysts. Dalton Trans. 2024, 53, 535. <https://doi.org/10.1039/D3DT02936K>
• Liu Shuai, Huang Kai-Yue, Liu Sha-Sha, He Yang, Zheng Yan, Li Lai-Cai: Substitution effects on the mechanism of Light-Induced 2,5-Diaryltetrazole-Naphthoquinone 1,3-Dipolar Cycloaddition: A theoretical study. Computational and Theoretical Chemistry 2023, 1222, 114060. <https://doi.org/10.1016/j.comptc.2023.114060>
• Li Niang-Xiu, Chen Yu-Mei, Xu Quan-Qing, Mu Wei-Hua: Photocatalytic reduction of CO2 to CO using nickel(II)-bipyridine complexes with different substituent groups as catalysts. Journal of CO2 Utilization 2023, 68, 102385. <https://doi.org/10.1016/j.jcou.2022.102385>
• Akita Munetaka, Ceroni Paola, Stephenson Corey R. J., Masson Géraldine: Progress in Photocatalysis for Organic Chemistry. J. Org. Chem. 2023, 88, 6281. <https://doi.org/10.1021/acs.joc.3c00812>
• Meyer Franc, Halasyamani P. Shiv, Masson Géraldine: Advances in Organic and Inorganic Photoredox Catalysis. ACS Org. Inorg. Au 2023, 3, 1. <https://doi.org/10.1021/acsorginorgau.2c00062>
• Rai Pratibha, Singh Jaya, Rai Pragati, Maurya Priyanka, Singh Jagdamba: Recent Development in Visible-Light Assisted, Photocatalyst Free Carbon-Heteroatom Bond Formation: review. Polycyclic Aromatic Compounds 2023, 1. <https://doi.org/10.1080/10406638.2023.2263609>
• Patel Geetika, Patel Ashok Raj, Banerjee Subhash: Sustainability of Visible Light-Driven Organic Transformations - A Review. COC 2023, 27, 166. <https://doi.org/10.2174/1385272827666221229110656>
• Ahmad Muhammad Siddique, Lin Po-Han, Zhang Qing, Zeng Bing, Wang Qifeng, Meguellati Kamel: Visible Light Induced C-H/N-H and C-X Bonds Reactions. Reactions 2023, 4, 189. <https://doi.org/10.3390/reactions4010012>
• Saikia B. Shriya, Deb Mohit L., Baruah Pranjal K.: Green synthesis of 1,3-oxazines by visible light-promoted catalyst-free C–H activation/cyclization of tertiary amines. Environ Chem Lett 2022, 20, 109. <https://doi.org/10.1007/s10311-021-01308-6>
• Castellanos-Soriano Jorge, Álvarez-Gutiérrez Daniel, Jiménez M. Consuelo, Pérez-Ruiz Raúl: Photoredox catalysis powered by triplet fusion upconversion: arylation of heteroarenes. Photochem Photobiol Sci 2022, 21, 1175. <https://doi.org/10.1007/s43630-022-00203-5>
• Rana Priksha, Singh Nishi, Majumdar Poulomi, Prakash Singh Surya: Evolution of BODIPY/aza-BODIPY dyes for organic photoredox/energy transfer catalysis. Coordination Chemistry Reviews 2022, 470, 214698. <https://doi.org/10.1016/j.ccr.2022.214698>
• Pitre Spencer P., Overman Larry E.: Strategic Use of Visible-Light Photoredox Catalysis in Natural Product Synthesis. Chem. Rev. 2022, 122, 1717. <https://doi.org/10.1021/acs.chemrev.1c00247>
• Holmberg-Douglas Natalie, Nicewicz David A.: Photoredox-Catalyzed C–H Functionalization Reactions. Chem. Rev. 2022, 122, 1925. <https://doi.org/10.1021/acs.chemrev.1c00311>
• Gupta Anamika, Iqbal Safia, Roohi, Hussain Mohd. Kamil, Zaheer Mohd. Rehan, Shankar Krapa: Visible Light-Promoted Green and Sustainable Approach for One-Pot Synthesis of 4,4’-(Arylmethylene)bis(1H-pyrazol-5-ols), In Vitro Anticancer Activity, and Molecular Docking with Covid-19 Mpro. ACS Omega 2022, 7, 34583. <https://doi.org/10.1021/acsomega.2c04506>
• Tsuchiya Naoki, Sheppard Tom D., Nishikata Takashi: Tertiary Alkylative Suzuki–Miyaura Couplings. Synthesis 2022, 54, 2340. <https://doi.org/10.1055/a-1732-4597>
• Karmakar Sukhen, Silamkoti Arundutt, Meanwell Nicholas A., Mathur Arvind, Gupta Arun Kumar: Utilization of C(sp3)‐Carboxylic Acids and Their Redox‐Active Esters in Decarboxylative Carbon−Carbon Bond Formation. Adv Synth Catal 2021, 363, 3693. <https://doi.org/10.1002/adsc.202100314>
• Wang Youjia, Duan Ruochen, Wu Yanhui, Li Xulian, Deng Chao: Metal‐Free Synthesis of Diarylmethanes through Visible‐Light Induced Radical Reactions with Arylamines. ChemistrySelect 2021, 6, 6097. <https://doi.org/10.1002/slct.202101388>
• Ren Shujian, Fu Jiahui, Cheng Dongping, Li Xiaonian, Xu Xiaoliang: A facile access for multisubstituted trifluoromethyl olefins by visible light catalysis. Tetrahedron Letters 2021, 66, 152829. <https://doi.org/10.1016/j.tetlet.2021.152829>
• Ren Shujian, Cheng Dongping, Li Xiaonian, Xu Xiaoliang: Mild oxidation of benzyl alcohols to benzyl aldehydes or ketones catalyzed by visible light. Tetrahedron Letters 2021, 76, 153234. <https://doi.org/10.1016/j.tetlet.2021.153234>
• Das Biswanath, Rahaman Ahibur, Shatskiy Andrey, Verho Oscar, Kärkäs Markus D., Åkermark Björn: The Impact of Ligand Carboxylates on Electrocatalyzed Water Oxidation. Acc. Chem. Res. 2021, 54, 3326. <https://doi.org/10.1021/acs.accounts.1c00298>
• Tian Ya-Ming, Guo Xiao-Ning, Braunschweig Holger, Radius Udo, Marder Todd B.: Photoinduced Borylation for the Synthesis of Organoboron Compounds. Chem. Rev. 2021, 121, 3561. <https://doi.org/10.1021/acs.chemrev.0c01236>
• Kos Martin, Rodríguez Rafael, Storch Jan, Sýkora Jan, Caytan Elsa, Cordier Marie, Císařová Ivana, Vanthuyne Nicolas, Williams J. A. Gareth, Žádný Jaroslav, Církva Vladimír, Crassous Jeanne: Enantioenriched Ruthenium-Tris-Bipyridine Complexes Bearing One Helical Bipyridine Ligand: Access to Fused Multihelicenic Systems and Chiroptical Redox Switches. Inorg. Chem. 2021, 60, 11838. <https://doi.org/10.1021/acs.inorgchem.1c01379>
• Liu Hong-Kun, Lei Yi-Fei, Tian Peng-Ju, Wang Hui, Zhao Xin, Li Zhan-Ting, Zhang Dan-Wei: [Fe(bpy)3]2+-based porous organic polymers with boosted photocatalytic activity for recyclable organic transformations. J. Mater. Chem. A 2021, 9, 6361. <https://doi.org/10.1039/D0TA12267J>
• Kim Se Hyun, An Ju Hyeon, Lee Jun Hee: Highly chemoselective deoxygenation of N-heterocyclic N-oxides under transition metal-free conditions. Org. Biomol. Chem. 2021, 19, 3735. <https://doi.org/10.1039/D1OB00260K>
• Dutta Arup, Rahman Noimur, Kumar John Elisa, Rabha Jintu, Phukan Tridip, Nongkhlaw Rishanlang: Catalyst-free UV365-assisted synthesis of pyran annulated heterocyclic scaffolds and evaluation of their antibacterial activities. Synthetic Communications 2021, 51, 263. <https://doi.org/10.1080/00397911.2020.1825741>
• Zenkov I. S., Yakushev A. A., Abel A. S., Averin A. D., Bessmertnykh-Lemeune A. G., Beletskaya I. P.: Photocatalytic Activity of Ruthenium(II) Complex with 1,10-Phenanthroline-3,8-dicarboxylic Acid in Aerobic Oxidation Reactions. Russ J Org Chem 2021, 57, 1398. <https://doi.org/10.1134/S1070428021090025>
• Zhao Yizhou, Wang Lanning, Song Tinglu, Mudryi Alexander, Li Yujing, Chen Qi: Recent Progress in Designing Halide-Perovskite-Based System for the Photocatalytic Applications. Front. Chem. 2021, 8. <https://doi.org/10.3389/fchem.2020.613174>
• Zhang Yajing, Wang Qian, Yan Zongsheng, Ma Donglai, Zheng Yuguang: Visible-light-mediated copper photocatalysis for organic syntheses. Beilstein J. Org. Chem. 2021, 17, 2520. <https://doi.org/10.3762/bjoc.17.169>
• Zhu Da‐Liang, Wu Qi, Li Hai‐Yan, Li Hong‐Xi, Lang Jian‐Ping: Hantzsch Ester as a Visible‐Light Photoredox Catalyst for Transition‐Metal‐Free Coupling of Arylhalides and Arylsulfinates. Chemistry A European J 2020, 26, 3484. <https://doi.org/10.1002/chem.201905281>
• Zidan Montserrat, Morris Avery O., McCallum Terry, Barriault Louis: The Alkylation and Reduction of Heteroarenes with Alcohols Using Photoredox Catalyzed Hydrogen Atom Transfer via Chlorine Atom Generation. Eur J Org Chem 2020, 2020, 1453. <https://doi.org/10.1002/ejoc.201900786>
• Gualandi Andrea, Marchini Marianna, Mengozzi Luca, Kidanu Hagos Tesfay, Franc Antoine, Ceroni Paola, Cozzi Pier Giorgio: Aluminum(III) Salen Complexes as Active Photoredox Catalysts. Eur J Org Chem 2020, 2020, 1486. <https://doi.org/10.1002/ejoc.201901086>
• Barthelemy Anne‐Laure, Dagousset Guillaume, Magnier Emmanuel: Metal‐Free Visible‐Light‐Mediated Hydrotrifluoromethylation of Unactivated Alkenes and Alkynes in Continuous Flow. Eur J Org Chem 2020, 2020, 1429. <https://doi.org/10.1002/ejoc.201901252>
• Fuks Elina, Huber Laura, Schinkel Thea, Trapp Oliver: Investigation of Straightforward, Photoinduced Alkylations of Electron‐Rich Heterocompounds with Electron‐Deficient Alkyl Bromides in the Sole Presence of 2,6‐Lutidine. Eur J Org Chem 2020, 2020, 6192. <https://doi.org/10.1002/ejoc.202001003>
• Qiao Shanshan, Feng Chao, Guo Yuan, Chen Tingxiang, Akram Naeem, Zhang Yi, Wang Wei, Yue Fan, Wang Jide: CdS nanoparticles modified Ni@NiO spheres as photocatalyst for oxygen production in water oxidation system and hydrogen production in water reduction system. Chemical Engineering Journal 2020, 395, 125068. <https://doi.org/10.1016/j.cej.2020.125068>
• Qiao Shanshan, Guo Jia, Wang Di, Zhang Liugen, Hassan Afaq, Chen Tingxiang, Feng Chao, Zhang Yi, Wang Jide: Core-shell cobalt particles Co@CoO loaded on nitrogen-doped graphene for photocatalytic water-splitting. International Journal of Hydrogen Energy 2020, 45, 1629. <https://doi.org/10.1016/j.ijhydene.2019.10.157>
• Sun Wencheng, Teng Qiaoling, Cheng Dongping, Li Xiaonian, Xu Xiaoliang: The hydrodebromination of 1,1-dibromoalkenes via visible light catalysis. Tetrahedron Letters 2020, 61, 151410. <https://doi.org/10.1016/j.tetlet.2019.151410>
• Pagire Santosh K., Föll Thomas, Reiser Oliver: Shining Visible Light on Vinyl Halides: Expanding the Horizons of Photocatalysis. Acc. Chem. Res. 2020, 53, 782. <https://doi.org/10.1021/acs.accounts.9b00615>
• Karbakhsh Ravari Alireza, Pineda-Galvan Yuliana, Huynh Alexander, Ezhov Roman, Pushkar Yulia: Facile Light-Induced Transformation of [RuII(bpy)2(bpyNO)]2+ to [RuII(bpy)3]2+. Inorg. Chem. 2020, 59, 13880. <https://doi.org/10.1021/acs.inorgchem.0c01446>
• Pagire Santosh K., Kumagai Naoya, Shibasaki Masakatsu: The Different Faces of [Ru(bpy)3Cl2] and fac[Ir(ppy)3] Photocatalysts: Redox Potential Controlled Synthesis of Sulfonylated Fluorenes and Pyrroloindoles from Unactivated Olefins and Sulfonyl Chlorides. Org. Lett. 2020, 22, 7853. <https://doi.org/10.1021/acs.orglett.0c02760>
• Gao Zhong-Zheng, Xu Yan-Yan, Wang Ze-Kun, Wang Hui, Zhang Dan-Wei, Li Zhan-Ting: Porous [Ru(bpy)3]2+-Cored Metallosupramolecular Polymers: Preparation and Recyclable Photocatalysis for the Formation of Amides and 2-Diazo-2-phenylacetates. ACS Appl. Polym. Mater. 2020, 2, 4885. <https://doi.org/10.1021/acsapm.0c00800>
• Liu Yanhong, Yang Yiying, Zhu Rongxiu, Zhang Dongju: Computational Clarification of Synergetic RuII/CuI-Metallaphotoredox Catalysis in C(sp3)–N Cross-Coupling Reactions of Alkyl Redox-Active Esters with Anilines. ACS Catal. 2020, 10, 5030. <https://doi.org/10.1021/acscatal.0c00060>
• Cheng Wan-Min, Shang Rui: Transition Metal-Catalyzed Organic Reactions under Visible Light: Recent Developments and Future Perspectives. ACS Catal. 2020, 10, 9170. <https://doi.org/10.1021/acscatal.0c01979>
• Luo Yi, Xu Zi-Yue, Wang Hui, Sun Xing-Wen, Li Zhan-Ting, Zhang Dan-Wei: Porous Ru(bpy)32+-Linked Polymers for Recyclable Photocatalysis of Enantioselective Alkylation of Aldehydes. ACS Macro Lett. 2020, 9, 90. <https://doi.org/10.1021/acsmacrolett.9b00872>
• Gualandi Andrea, Calogero Francesco, Martinelli Ada, Quintavalla Arianna, Marchini Marianna, Ceroni Paola, Lombardo Marco, Cozzi Pier Giorgio: A supramolecular bifunctional iridium photoaminocatalyst for the enantioselective alkylation of aldehydes. Dalton Trans. 2020, 49, 14497. <https://doi.org/10.1039/D0DT02587A>
• Waki Minoru, Shirai Soichi, Yamanaka Ken-ichi, Maegawa Yoshifumi, Inagaki Shinji: Heterogeneous water oxidation photocatalysis based on periodic mesoporous organosilica immobilizing a tris(2,2′-bipyridine)ruthenium sensitizer. RSC Adv. 2020, 10, 13960. <https://doi.org/10.1039/D0RA00895H>
• Yang Xue, Zhang Suyuan, Li Peixian, Gao Shuiying, Cao Rong: Visible-light-driven photocatalytic selective organic oxidation reactions. J. Mater. Chem. A 2020, 8, 20897. <https://doi.org/10.1039/D0TA05485B>
• Jain A., Ameta C.: Novel Way to Harness Solar Energy: Photo-Redox Catalysis in Organic Synthesis. Kinet Catal 2020, 61, 242. <https://doi.org/10.1134/S002315842002007X>
• Ho Yee Ann, Paffenholz Eva, Kim Hyun Jin, Orgis Benjamin, Rueping Magnus, Fabry David C.: Catalytic Wacker‐type Oxidations Using Visible Light Photoredox Catalysis. ChemCatChem 2019, 11, 1889. <https://doi.org/10.1002/cctc.201900271>
• Loibl Antonia, Weber Manuela, Lutz Martin, Müller Christian: ReI Complexes of Pyridylphosphinines and 2,2′‐Bipyridine Derivatives: A Comparison. Eur J Inorg Chem 2019, 2019, 1575. <https://doi.org/10.1002/ejic.201801234>
• Lekkala Ravindar, Lekkala Revathi, Moku Balakrishna, Rakesh K. P., Qin Hua‐Li: Recent Developments in Radical‐Mediated Transformations of Organohalides. Eur J Org Chem 2019, 2019, 2769. <https://doi.org/10.1002/ejoc.201900098>
• Wu Yi-Peng, Yan Meng, Gao Zhong-Zheng, Hou Jun-Li, Wang Hui, Zhang Dan-Wei, Zhang Junliang, Li Zhan-Ting: Ruthenium(II)-cored supramolecular organic framework-mediated recyclable visible light photoreduction of azides to amines and cascade formation of lactams. Chinese Chemical Letters 2019, 30, 1383. <https://doi.org/10.1016/j.cclet.2019.03.056>
• Luis Ena T., Iranmanesh Hasti, Beves Jonathon E.: Photosubstitution reactions in ruthenium(II) trisdiimine complexes: Implications for photoredox catalysis. Polyhedron 2019, 160, 1. <https://doi.org/10.1016/j.poly.2018.11.057>
• Weng Jian-Quan, Xu Wen-Xiu, Dai Xiao-Qiang, Zhang Jun-Hui, Liu Xing-Hai: Alkylation reactions of benzothiazoles with N,N-dimethylamides catalyzed by the two-component system under visible light. Tetrahedron Letters 2019, 60, 390. <https://doi.org/10.1016/j.tetlet.2018.12.064>
• Ye Hongqiang, Zhao He, Ren Shujian, Ye Hongfeng, Cheng Dongping, Li Xiaonian, Xu Xiaoliang: The coupling of alkylboronic acids and esters with Baylis–Hillman derivatives by Lewis base/photoredox dual catalysis. Tetrahedron Letters 2019, 60, 1302. <https://doi.org/10.1016/j.tetlet.2019.04.015>
• Ren Xiang, Lu Zhan: Visible light promoted difunctionalization reactions of alkynes. Chinese Journal of Catalysis 2019, 40, 1003. <https://doi.org/10.1016/S1872-2067(19)63278-X>
• Prasanna Ramanathan, Guha Somraj, Sekar Govindasamy: Proton-Coupled Electron Transfer: Transition-Metal-Free Selective Reduction of Chalcones and Alkynes Using Xanthate/Formic Acid. Org. Lett. 2019, 21, 2650. <https://doi.org/10.1021/acs.orglett.9b00635>
• Lyu Xue-Li, Huang Shi-Sheng, Song Hong-Jian, Liu Yu-Xiu, Wang Qing-Min: Visible-Light-Induced Copper-Catalyzed Decarboxylative Coupling of Redox-Active Esters with N-Heteroarenes. Org. Lett. 2019, 21, 5728. <https://doi.org/10.1021/acs.orglett.9b02105>
• Chang Chao-Wan, Cheng Ming-Chuan, Lee Gene-Hsiang, Peng Shie-Ming: Facile synthesis of 1,5-disubstituted tetrazoles by reacting a ruthenium acetylide complex with trimethylsilyl azide. Dalton Trans. 2019, 48, 11732. <https://doi.org/10.1039/C9DT02363A>
• Teplý Filip: Visible-light photoredox catalysis with [Ru(bpy)3]2+: General principles and the twentieth-century roots. Physical Sciences Reviews 2019, 0. <https://doi.org/10.1515/psr-2017-0171>
• Zeitler Kirsten, Neumann Matthias: Synergistic visible light photoredox catalysis. Physical Sciences Reviews 2019, 0. <https://doi.org/10.1515/psr-2017-0173>
• Rai Vijai K., Verma Fooleswar, Mahata Suhasini, Bhardiya Smita R., Singh Manorama, Rai Ankita: Metal Doped-C3N4/Fe2O4: Efficient and Versatile Heterogenous Catalysts for Organic Transformations. COC 2019, 23, 1284. <https://doi.org/10.2174/1385272823666190709113758>
• Hatakeda Miho, Toohara Souta, Nakashima Takuya, Sakurai Shinichi, Kuroiwa Keita: Helical-Ribbon and Tape Formation of Lipid Packaged [Ru(bpy)3]2+ Complexes in Organic Media. IJMS 2019, 20, 3298. <https://doi.org/10.3390/ijms20133298>
• Zhu Jie, Yang Wen‐Chao, Wang Xiao‐dong, Wu Lei: Photoredox Catalysis in C–S Bond Construction: Recent Progress in Photo‐Catalyzed Formation of Sulfones and Sulfoxides. Adv Synth Catal 2018, 360, 386. <https://doi.org/10.1002/adsc.201701194>
• Tripathi Shubhangi, Kapoor Ritu, Yadav Lal Dhar S.: Visible Light Activated Radical Denitrative Benzoylation of β‐Nitrostyrenes: A Photocatalytic Approach to Chalcones. Adv Synth Catal 2018, 360, 1407. <https://doi.org/10.1002/adsc.201701559>
• Revathi Lekkala, Ravindar Lekkala, Fang Wan‐Yin, Rakesh K. P., Qin Hua‐Li: Visible Light‐Induced C−H Bond Functionalization: A Critical Review. Adv Synth Catal 2018, 360, 4652. <https://doi.org/10.1002/adsc.201800736>
• Dmitriev Igor A., Supranovich Vyacheslav I., Levin Vitalij V., Struchkova Marina I., Dilman Alexander D.: Visible Light Promoted 2‐Bromotetrafluoroethylation of Nitrones. Adv Synth Catal 2018, 360, 3788. <https://doi.org/10.1002/adsc.201800802>
• Marzo Leyre, Pagire Santosh K., Reiser Oliver, König Burkhard: Photokatalyse mit sichtbarem Licht: Welche Bedeutung hat sie für die organische Synthese?. Angewandte Chemie 2018, 130, 10188. <https://doi.org/10.1002/ange.201709766>
• Barthelemy Anne‐Laure, Tuccio Béatrice, Magnier Emmanuel, Dagousset Guillaume: Alkoxyl Radicals Generated under Photoredox Catalysis: A Strategy for anti‐Markovnikov Alkoxylation Reactions. Angewandte Chemie 2018, 130, 13986. <https://doi.org/10.1002/ange.201806522>
• Marzo Leyre, Pagire Santosh K., Reiser Oliver, König Burkhard: Visible‐Light Photocatalysis: Does It Make a Difference in Organic Synthesis?. Angew Chem Int Ed 2018, 57, 10034. <https://doi.org/10.1002/anie.201709766>
• Barthelemy Anne‐Laure, Tuccio Béatrice, Magnier Emmanuel, Dagousset Guillaume: Alkoxyl Radicals Generated under Photoredox Catalysis: A Strategy for anti‐Markovnikov Alkoxylation Reactions. Angew Chem Int Ed 2018, 57, 13790. <https://doi.org/10.1002/anie.201806522>
• Hou Hong, Zhu Shaoqun, Atodiresei Iuliana, Rueping Magnus: Asymmetric Organocatalysis and Photoredox Catalysis for the α‐Functionalization of Tetrahydroisoquinolines. Eur J Org Chem 2018, 2018, 1277. <https://doi.org/10.1002/ejoc.201800117>
• McGee Philippe, Brousseau Julie, Barriault Louis: Development of New Gold (I)‐Catalyzed Carbocyclizations and their Applications in the Synthesis of Natural Products. Israel Journal of Chemistry 2018, 58, 511. <https://doi.org/10.1002/ijch.201700054>
• López-Calixto Carmen G., Liras Marta, de la Peña O’Shea Victor A., Pérez-Ruiz Raúl: Synchronized biphotonic process triggering C C coupling catalytic reactions. Applied Catalysis B: Environmental 2018, 237, 18. <https://doi.org/10.1016/j.apcatb.2018.05.062>
• Michelin Clément, Hoffmann Norbert: Photocatalysis applied to organic synthesis – A green chemistry approach. Current Opinion in Green and Sustainable Chemistry 2018, 10, 40. <https://doi.org/10.1016/j.cogsc.2018.02.009>
• Ye Hongqiang, Ye Qianwen, Cheng Dongping, Li Xiaonian, Xu Xiaoliang: The coupling of potassium organotrifluoroborates with Baylis–Hillman derivatives via visible-light photoredox catalysis. Tetrahedron Letters 2018, 59, 2046. <https://doi.org/10.1016/j.tetlet.2018.04.035>
• Hong Dachao, Tsukakoshi Yuto, Kotani Hiroaki, Ishizuka Tomoya, Ohkubo Kei, Shiota Yoshihito, Yoshizawa Kazunari, Fukuzumi Shunichi, Kojima Takahiko: Mechanistic Insights into Homogeneous Electrocatalytic and Photocatalytic Hydrogen Evolution Catalyzed by High-Spin Ni(II) Complexes with S2N2-Type Tetradentate Ligands. Inorg. Chem. 2018, 57, 7180. <https://doi.org/10.1021/acs.inorgchem.8b00881>
• Pagire Santosh K., Hossain Asik, Reiser Oliver: Temperature Controlled Selective C–S or C–C Bond Formation: Photocatalytic Sulfonylation versus Arylation of Unactivated Heterocycles Utilizing Aryl Sulfonyl Chlorides. Org. Lett. 2018, 20, 648. <https://doi.org/10.1021/acs.orglett.7b03790>
• Li Run, Byun Jeehye, Huang Wei, Ayed Cyrine, Wang Lei, Zhang Kai A. I.: Poly(benzothiadiazoles) and Their Derivatives as Heterogeneous Photocatalysts for Visible-Light-Driven Chemical Transformations. ACS Catal. 2018, 8, 4735. <https://doi.org/10.1021/acscatal.8b00407>
• Tripathi Shubhangi, Yadav Lal Dhar S.: Visible-light-enabled denitrative carboxylation of β-nitrostyrenes: a direct photocatalytic approach to cinnamic acids. New J. Chem. 2018, 42, 3765. <https://doi.org/10.1039/C7NJ04578F>
• Verma Fooleswar, Sahu Anjumala, Singh Puneet K., Rai Ankita, Singh Manorama, Rai Vijai K.: Visible-light driven regioselective synthesis of 1H-tetrazoles from aldehydes through isocyanide-based [3 + 2] cycloaddition. Green Chem. 2018, 20, 3783. <https://doi.org/10.1039/C8GC01321G>
• Zhang Xu, Rakesh K. P., Ravindar L., Qin Hua-Li: Visible-light initiated aerobic oxidations: a critical review. Green Chem. 2018, 20, 4790. <https://doi.org/10.1039/C8GC02382D>
• Nongthombam Geetmani Singh, Kharmawlong George Kupar, Kumar John Elisa, Nongkhlaw Rishanlang: UV365 light promoted catalyst-free synthesis of pyrimido[4,5-b]quinoline-2,4-diones in aqueous-glycerol medium. New J. Chem. 2018, 42, 9436. <https://doi.org/10.1039/C8NJ01459K>
• Kibriya Golam, Bagdi Avik K., Hajra Alakananda: Visible light induced tetramethylethylenediamine assisted formylation of imidazopyridines. Org. Biomol. Chem. 2018, 16, 3473. <https://doi.org/10.1039/C8OB00532J>
• Erdmann E., Villinger A., König B., Seidel W. W.: 1,10-Phenanthroline-dithiine iridium and ruthenium complexes: synthesis, characterization and photocatalytic dihydrogen evolution. Photochem Photobiol Sci 2018, 17, 1056. <https://doi.org/10.1039/c8pp00068a>
• Khan Raysa, Boonseng Sarote, Kemmitt Paul D., Felix Robert, Coles Simon J., Tizzard Graham J., Williams Gareth, Simmonds Olivia, Harvey Jessica‐Lily, Atack John, Cox Hazel, Spencer John: Combining Sanford Arylations on Benzodiazepines with the Nuisance Effect. Adv Synth Catal 2017, 359, 3261. <https://doi.org/10.1002/adsc.201700626>
• Daniel Marion, Dagousset Guillaume, Diter Patrick, Klein Pierre‐André, Tuccio Béatrice, Goncalves Anne‐Marie, Masson Géraldine, Magnier Emmanuel: Fluorinated Sulfilimino Iminiums: Efficient and Versatile Sources of Perfluoroalkyl Radicals under Photoredox Catalysis. Angewandte Chemie 2017, 129, 4055. <https://doi.org/10.1002/ange.201700290>
• Pagire Santosh K., Kreitmeier Peter, Reiser Oliver: Bildung von α‐Ketoradikalen aus Vinylbromiden und molekularem Sauerstoff mit sichtbarem Licht: Synthese von Indenonen und Dihydroindeno[1,2‐c]chromenen. Angewandte Chemie 2017, 129, 11068. <https://doi.org/10.1002/ange.201702953>
• Daniel Marion, Dagousset Guillaume, Diter Patrick, Klein Pierre‐André, Tuccio Béatrice, Goncalves Anne‐Marie, Masson Géraldine, Magnier Emmanuel: Fluorinated Sulfilimino Iminiums: Efficient and Versatile Sources of Perfluoroalkyl Radicals under Photoredox Catalysis. Angew Chem Int Ed 2017, 56, 3997. <https://doi.org/10.1002/anie.201700290>
• Pagire Santosh K., Kreitmeier Peter, Reiser Oliver: Visible‐Light‐Promoted Generation of α‐Ketoradicals from Vinyl‐bromides and Molecular Oxygen: Synthesis of Indenones and Dihydroindeno[1,2‐c]chromenes. Angew Chem Int Ed 2017, 56, 10928. <https://doi.org/10.1002/anie.201702953>
• Pettersson Fredrik, Bergonzini Giulia, Cassani Carlo, Wallentin Carl‐Johan: Redox‐Neutral Dual Functionalization of Electron‐Deficient Alkenes. Chemistry A European J 2017, 23, 7444. <https://doi.org/10.1002/chem.201701589>
• Hoffmann Norbert: Proton‐Coupled Electron Transfer in Photoredox Catalytic Reactions. Eur J Org Chem 2017, 2017, 1982. <https://doi.org/10.1002/ejoc.201601445>
• Santacroce Veronica, Duboc Raphael, Malacria Max, Maestri Giovanni, Masson Geraldine: Visible‐Light, Photoredox‐Mediated Oxidative Tandem Nitroso‐Diels–Alder Reaction of Arylhydroxylamines with Conjugated Dienes. Eur J Org Chem 2017, 2017, 2095. <https://doi.org/10.1002/ejoc.201601492>
• Meyer Andreas Uwe, Lau Vincent Wing‐hei, König Burkhard, Lotsch Bettina V.: Photocatalytic Oxidation of Sulfinates to Vinyl Sulfones with Cyanamide‐Functionalised Carbon Nitride. Eur J Org Chem 2017, 2017, 2179. <https://doi.org/10.1002/ejoc.201601637>
• Boubertakh Oualid, Goddard Jean‐Philippe: Construction and Functionalization of Heteroarenes by Use of Photoredox Catalysis. Eur J Org Chem 2017, 2017, 2072. <https://doi.org/10.1002/ejoc.201601653>
• Eisenhofer Anna, Hioe Johnny, Gschwind Ruth M., König Burkhard: Photocatalytic Phenol–Arene C–C and C–O Cross‐Dehydrogenative Coupling. Eur J Org Chem 2017, 2017, 2194. <https://doi.org/10.1002/ejoc.201700211>
• Sázelová Petra, Koval Dušan, Severa Lukáš, Teplý Filip, Kašička Václav: Chiral analysis of α‐diimine Ru(II) and Fe(II) complexes by capillary electrophoresis using sulfated cyclodextrins as stereoselectors. Electrophoresis 2017, 38, 1913. <https://doi.org/10.1002/elps.201700077>
• Mishra Anu, Rai Pratibha, Srivastava Madhulika, Tripathi Bhartendu Pati, Yadav Snehlata, Singh Jaya, Singh Jagdamba: A Peerless Aproach: Organophotoredox/Cu(I) Catalyzed, Regioselective, Visible Light Facilitated, Click Synthesis of 1,2,3-Triazoles via Azide–Alkyne [3 + 2] Cycloaddition. Catal Lett 2017, 147, 2600. <https://doi.org/10.1007/s10562-017-2156-8>
• Swavey Shawn, Ireland David, Irwin Emily, Counts Jacob: Synthesis, spectroscopic, and electrochemical studies of bis-ruthenium(II) polypyridyl complexes bridged by dipyrromethenes. Inorganica Chimica Acta 2017, 454, 71. <https://doi.org/10.1016/j.ica.2016.03.008>
• Borpatra Paran J., Deb Mohit L., Baruah Pranjal K.: Visible light-promoted metal-free intramolecular cross dehydrogenative coupling approach to 1,3-oxazines. Tetrahedron Letters 2017, 58, 4006. <https://doi.org/10.1016/j.tetlet.2017.09.018>
• Shang Jinting, Tang Hanying, Ji Hongwei, Ma Wanhong, Chen Chuncheng, Zhao Jincai: Synthesis, characterization, and activity of a covalently anchored heterogeneous perylene diimide photocatalyst. Chinese Journal of Catalysis 2017, 38, 2094. <https://doi.org/10.1016/S1872-2067(17)62960-7>
• Kumamoto Kota, Tsuchibashi Kenta, Pramata Azzah Dyah, Yuasa Masayoshi, Shimanoe Kengo, Kida Tetsuya: Visible Light-Driven Photoenergy Storage and Photocatalysis Using Polyoxometallates Coupled with a Ru Complex. J. Phys. Chem. C 2017, 121, 13515. <https://doi.org/10.1021/acs.jpcc.7b02484>
• Zhao Quan-Qing, Chen Jun, Yan Dong-Mei, Chen Jia-Rong, Xiao Wen-Jing: Photocatalytic Hydrazonyl Radical-Mediated Radical Cyclization/Allylation Cascade: Synthesis of Dihydropyrazoles and Tetrahydropyridazines. Org. Lett. 2017, 19, 3620. <https://doi.org/10.1021/acs.orglett.7b01609>
• Kärkäs Markus D.: Photochemical Generation of Nitrogen-Centered Amidyl, Hydrazonyl, and Imidyl Radicals: Methodology Developments and Catalytic Applications. ACS Catal. 2017, 7, 4999. <https://doi.org/10.1021/acscatal.7b01385>
• Yang Bo, Lu Zhan: Visible-Light-Promoted Metal-Free Aerobic Hydroxyazidation of Alkenes. ACS Catal. 2017, 7, 8362. <https://doi.org/10.1021/acscatal.7b02892>
• Hong Dachao, Tsukakoshi Yuto, Kotani Hiroaki, Ishizuka Tomoya, Kojima Takahiko: Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production. J. Am. Chem. Soc. 2017, 139, 6538. <https://doi.org/10.1021/jacs.7b01956>
• Pagire Santosh K., Hossain Asik, Traub Lukas, Kerres Sabine, Reiser Oliver: Photosensitised regioselective [2+2]-cycloaddition of cinnamates and related alkenes. Chem. Commun. 2017, 53, 12072. <https://doi.org/10.1039/C7CC06710K>
• Marin Mireia, Miranda Miguel A., Marin M. Luisa: A comprehensive mechanistic study on the visible-light photocatalytic reductive dehalogenation of haloaromatics mediated by Ru(bpy)3Cl2. Catal. Sci. Technol. 2017, 7, 4852. <https://doi.org/10.1039/C7CY01231D>
• Li Yuewen, Lu Yiye, Mao Runyu, Li Zhiming, Wu Jie: A photoinduced reaction of perfluoroalkyl halides with 1,3-diarylprop-2-yn-1-ones catalyzed by DABSO. Org. Chem. Front. 2017, 4, 1745. <https://doi.org/10.1039/C7QO00279C>
• Srivastava Vishal, Singh Praveen P.: Eosin Y catalysed photoredox synthesis: a review. RSC Adv. 2017, 7, 31377. <https://doi.org/10.1039/C7RA05444K>
• Cai Xiaohui, Liu Hanwen, Zhi Lihua, Wen Huang, Yu Ailing, Li Lianhua, Chen Fengjuan, Wang Baodui: A g-C3N4/rGO nanocomposite as a highly efficient metal-free photocatalyst for direct C–H arylation under visible light irradiation. RSC Adv. 2017, 7, 46132. <https://doi.org/10.1039/C7RA07462J>
• Li Yang, Liu Bang, Song Ren‐Jie, Wang Qiu‐An, Li Jin‐Heng: Visible Light‐Initiated C(sp3)Br/C(sp3)H Functionalization of α‐Carbonyl Alkyl Bromides through Hydride Radical Shift. Adv Synth Catal 2016, 358, 1219. <https://doi.org/10.1002/adsc.201501134>
• Zhang Heng, Huang Xueliang: Ligand‐Free Heck Reactions of Aryl Iodides: Significant Acceleration of the Rate through Visible Light Irradiation at Ambient Temperature. Adv Synth Catal 2016, 358, 3736. <https://doi.org/10.1002/adsc.201600704>
• Suzuki Itaru, Esumi Naoto, Yasuda Makoto: Photoredox α‐Allylation of α‐Halocarbonyls with Allylboron Compounds Accelerated by Fluoride Salts under Visible Light Irradiation. Asian J Org Chem 2016, 5, 179. <https://doi.org/10.1002/ajoc.201500475>
• Wang Chuanyong, Qin Jie, Shen Xiaodong, Riedel Radostan, Harms Klaus, Meggers Eric: Asymmetric Radical–Radical Cross‐Coupling through Visible‐Light‐Activated Iridium Catalysis. Angewandte Chemie 2016, 128, 695. <https://doi.org/10.1002/ange.201509524>
• Fava Eleonora, Millet Anthony, Nakajima Masaki, Loescher Sebastian, Rueping Magnus: Reduktive Umpolung von Carbonylderivaten mittels Photoredoxkatalyse mit sichtbarem Licht: ein direkter Zugang zu vicinalen Diaminen und Aminoalkoholen über α‐Aminoradikale und Ketylradikale. Angewandte Chemie 2016, 128, 6888. <https://doi.org/10.1002/ange.201511235>
• Hopkinson Matthew N., Gómez‐Suárez Adrián, Teders Michael, Sahoo Basudev, Glorius Frank: Schnelles Entdecken photokatalytischer Reaktionen durch mechanismusbasiertes Screening. Angewandte Chemie 2016, 128, 4434. <https://doi.org/10.1002/ange.201600995>
• Wang Chuanyong, Qin Jie, Shen Xiaodong, Riedel Radostan, Harms Klaus, Meggers Eric: Asymmetric Radical–Radical Cross‐Coupling through Visible‐Light‐Activated Iridium Catalysis. Angew Chem Int Ed 2016, 55, 685. <https://doi.org/10.1002/anie.201509524>
• Fava Eleonora, Millet Anthony, Nakajima Masaki, Loescher Sebastian, Rueping Magnus: Reductive Umpolung of Carbonyl Derivatives with Visible‐Light Photoredox Catalysis: Direct Access to Vicinal Diamines and Amino Alcohols via α‐Amino Radicals and Ketyl Radicals. Angew Chem Int Ed 2016, 55, 6776. <https://doi.org/10.1002/anie.201511235>
• Hopkinson Matthew N., Gómez‐Suárez Adrián, Teders Michael, Sahoo Basudev, Glorius Frank: Accelerated Discovery in Photocatalysis using a Mechanism‐Based Screening Method. Angew Chem Int Ed 2016, 55, 4361. <https://doi.org/10.1002/anie.201600995>
• Bergonzini Giulia, Cassani Carlo, Lorimer‐Olsson Haldor, Hörberg Johanna, Wallentin Carl‐Johan: Visible‐Light‐Mediated Photocatalytic Difunctionalization of Olefins by Radical Acylarylation and Tandem Acylation/Semipinacol Rearrangement. Chemistry A European J 2016, 22, 3292. <https://doi.org/10.1002/chem.201504985>
• Honeker Roman, Garza‐Sanchez R. Aleyda, Hopkinson Matthew N., Glorius Frank: Visible‐Light‐Promoted Trifluoromethylthiolation of Styrenes by Dual Photoredox/Halide Catalysis. Chemistry A European J 2016, 22, 4395. <https://doi.org/10.1002/chem.201600190>
• Meyer Andreas Uwe, Straková Karolína, Slanina Tomáš, König Burkhard: Eosin Y (EY) Photoredox‐Catalyzed Sulfonylation of Alkenes: Scope and Mechanism. Chemistry A European J 2016, 22, 8694. <https://doi.org/10.1002/chem.201601000>
• Fan Lulu, Jia Jiaqi, Hou Hong, Lefebvre Quentin, Rueping Magnus: Decarboxylative Aminomethylation of Aryl‐ and Vinylsulfonates through Combined Nickel‐ and Photoredox‐Catalyzed Cross‐Coupling. Chemistry A European J 2016, 22, 16437. <https://doi.org/10.1002/chem.201604452>
• Christmann Julien, Ibrahim Ahmad, Charlot Vincent, Croutxé‐Barghorn Céline, Ley Christian, Allonas Xavier: Elucidation of the Key Role of [Ru(bpy)3]2+ in Photocatalyzed RAFT Polymerization. ChemPhysChem 2016, 17, 2309. <https://doi.org/10.1002/cphc.201600034>
• Das Santu, Lai Dipti, Mallick Apabrita, Roy Soumyajit: Photo Redox Mediated Inexpensive One-Pot Synthesis of 1,4-Diphenyl Substituted Butane-1,4-Dione from Styrene using Polyoxometalate as a Catalyst. ChemistrySelect 2016, 1, 691. <https://doi.org/10.1002/slct.201500052>
• Feng Zhujia, Zeng Tingting, Xuan Jun, Liu Yunhang, Lu Liangqiu, Xiao Wen-Jing: C–H allylation of N-aryl-tetrahydroisoquinolines by merging photoredox catalysis with iodide catalysis. Sci. China Chem. 2016, 59, 171. <https://doi.org/10.1007/s11426-015-5548-x>
• Gao Shuanhu, Qiu Yuanyou: Advances of radical and photo reactions in natural products synthesis. Sci. China Chem. 2016, 59, 1093. <https://doi.org/10.1007/s11426-016-0032-y>
• Vincent Guillaume, Cheli Saloua, Martinez Mallorquin Rocio, Abramovitch Adi, Beauvière Sophie, Gomez Catherine, Brebion Franck, Marek Ilan, Malacria Max, Goddard Jean Philippe, Fensterbank Louis: Oxidation of bis-sulfinyl carbanions as the pivot of ionic/radical tandem reactions. Comptes Rendus Chimie 2016, 19, 403. <https://doi.org/10.1016/j.crci.2015.11.012>
• Hering Thea, König Burkhard: Photocatalytic activation of N-chloro compounds for the chlorination of arenes. Tetrahedron 2016, 72, 7821. <https://doi.org/10.1016/j.tet.2016.06.028>
• Erbland Guillaume, Ruch Jonas, Goddard Jean-Philippe: Photochemical functionalization of diazines: metal-free vinylation and phosphonylation. Tetrahedron 2016, 72, 7826. <https://doi.org/10.1016/j.tet.2016.07.069>
• Yadav Vinod K., Srivastava Vishnu P., Yadav Lal Dhar S.: Visible-light-promoted cyclodesulfurization of phenolic thioureas: an organophotoredox catalytic approach to 2-aminobenzoxazoles. Tetrahedron Letters 2016, 57, 155. <https://doi.org/10.1016/j.tetlet.2015.11.089>
• Hou Tianyuan, Lu Ping, Li Pixu: Visible-light-mediated benzylic sp3 C–H bond functionalization to C–Br or C–N bond. Tetrahedron Letters 2016, 57, 2273. <https://doi.org/10.1016/j.tetlet.2016.04.036>
• Zhang Ying-Peng, Feng Xiao-Long, Yang Yun-Shang, Cao Bi-Xia: Metal-free, C–H arylation of indole and its derivatives with aryl diazonium salts by visible-light photoredox catalysis. Tetrahedron Letters 2016, 57, 2298. <https://doi.org/10.1016/j.tetlet.2016.04.051>
• Yadav Vinod K., Srivastava Vishnu P., Yadav Lal Dhar S.: Visible light induced azidation of aldehydic C–H with carbon tetrabromide and sodium azide. Tetrahedron Letters 2016, 57, 2502. <https://doi.org/10.1016/j.tetlet.2016.04.098>
• Morris Scott A., Wang Jiang, Zheng Nan: The Prowess of Photogenerated Amine Radical Cations in Cascade Reactions: From Carbocycles to Heterocycles. Acc. Chem. Res. 2016, 49, 1957. <https://doi.org/10.1021/acs.accounts.6b00263>
• Majek Michal, Jacobi von Wangelin Axel: Mechanistic Perspectives on Organic Photoredox Catalysis for Aromatic Substitutions. Acc. Chem. Res. 2016, 49, 2316. <https://doi.org/10.1021/acs.accounts.6b00293>
• Reiser Oliver: Shining Light on Copper: Unique Opportunities for Visible-Light-Catalyzed Atom Transfer Radical Addition Reactions and Related Processes. Acc. Chem. Res. 2016, 49, 1990. <https://doi.org/10.1021/acs.accounts.6b00296>
• Poplata Saner, Tröster Andreas, Zou You-Quan, Bach Thorsten: Recent Advances in the Synthesis of Cyclobutanes by Olefin [2 + 2] Photocycloaddition Reactions. Chem. Rev. 2016, 116, 9748. <https://doi.org/10.1021/acs.chemrev.5b00723>
• Kärkäs Markus D., Porco John A., Stephenson Corey R. J.: Photochemical Approaches to Complex Chemotypes: Applications in Natural Product Synthesis. Chem. Rev. 2016, 116, 9683. <https://doi.org/10.1021/acs.chemrev.5b00760>
• Skubi Kazimer L., Blum Travis R., Yoon Tehshik P.: Dual Catalysis Strategies in Photochemical Synthesis. Chem. Rev. 2016, 116, 10035. <https://doi.org/10.1021/acs.chemrev.6b00018>
• Afewerki Samson, Córdova Armando: Combinations of Aminocatalysts and Metal Catalysts: A Powerful Cooperative Approach in Selective Organic Synthesis. Chem. Rev. 2016, 116, 13512. <https://doi.org/10.1021/acs.chemrev.6b00226>
• Fan Xiu-Wei, Lei Tao, Zhou Chao, Meng Qing-Yuan, Chen Bin, Tung Chen-Ho, Wu Li-Zhu: Radical Addition of Hydrazones by α-Bromo Ketones To Prepare 1,3,5-Trisubstituted Pyrazoles via Visible Light Catalysis. J. Org. Chem. 2016, 81, 7127. <https://doi.org/10.1021/acs.joc.6b00992>
• Yang Bo, Lu Zhan: Visible-Light-Promoted Oxidative [4 + 2] Cycloadditions of Aryl Silyl Enol Ethers. J. Org. Chem. 2016, 81, 7288. <https://doi.org/10.1021/acs.joc.6b01016>
• Xia Zhonghua, Khaled Omar, Mouriès-Mansuy Virginie, Ollivier Cyril, Fensterbank Louis: Dual Photoredox/Gold Catalysis Arylative Cyclization of o-Alkynylphenols with Aryldiazonium Salts: A Flexible Synthesis of Benzofurans. J. Org. Chem. 2016, 81, 7182. <https://doi.org/10.1021/acs.joc.6b01060>
• Dong Wuheng, Hu Bei, Gao Xiaoshuang, Li Yuyuan, Xie Xiaomin, Zhang Zhaoguo: Visible-Light-Induced Photocatalytic Aerobic Oxidation/Povarov Cyclization Reaction: Synthesis of Substituted Quinoline-Fused Lactones. J. Org. Chem. 2016, 81, 8770. <https://doi.org/10.1021/acs.joc.6b01253>
• Gao Xiao-Fei, Du Jing-Jing, Liu Zheng, Guo Jun: Visible-Light-Induced Specific Desulfurization of Cysteinyl Peptide and Glycopeptide in Aqueous Solution. Org. Lett. 2016, 18, 1166. <https://doi.org/10.1021/acs.orglett.6b00292>
• Lebée Clément, Languet Morgan, Allain Clémence, Masson Géraldine: α-Carbamoylsulfides as N-Carbamoylimine Precursors in the Visible Light Photoredox-Catalyzed Synthesis of α,α-Disubstituted Amines. Org. Lett. 2016, 18, 1478. <https://doi.org/10.1021/acs.orglett.6b00442>
• Pagire Santosh K., Paria Suva, Reiser Oliver: Synthesis of β-Hydroxysulfones from Sulfonyl Chlorides and Alkenes Utilizing Visible Light Photocatalytic Sequences. Org. Lett. 2016, 18, 2106. <https://doi.org/10.1021/acs.orglett.6b00734>
• Cannillo Alexandre, Schwantje Travis R., Bégin Maxime, Barabé Francis, Barriault Louis: Gold-Catalyzed Photoredox C(sp2) Cyclization: Formal Synthesis of (±)-Triptolide. Org. Lett. 2016, 18, 2592. <https://doi.org/10.1021/acs.orglett.6b00968>
• Jarrige Lucie, Carboni Aude, Dagousset Guillaume, Levitre Guillaume, Magnier Emmanuel, Masson Géraldine: Photoredox-Catalyzed Three-Component Tandem Process: An Assembly of Complex Trifluoromethylated Phthalans and Isoindolines. Org. Lett. 2016, 18, 2906. <https://doi.org/10.1021/acs.orglett.6b01257>
• Esumi Naoto, Suzuki Kensuke, Nishimoto Yoshihiro, Yasuda Makoto: Synthesis of 1,4-Dicarbonyl Compounds from Silyl Enol Ethers and Bromocarbonyls, Catalyzed by an Organic Dye under Visible-Light Irradiation with Perfect Selectivity for the Halide Moiety over the Carbonyl Group. Org. Lett. 2016, 18, 5704. <https://doi.org/10.1021/acs.orglett.6b02869>
• Jin Yunhe, Yang Haijun, Fu Hua: Thiophenol-Catalyzed Visible-Light Photoredox Decarboxylative Couplings of N-(Acetoxy)phthalimides. Org. Lett. 2016, 18, 6400. <https://doi.org/10.1021/acs.orglett.6b03300>
• Luo Jian, Zhang Jian: Donor–Acceptor Fluorophores for Visible-Light-Promoted Organic Synthesis: Photoredox/Ni Dual Catalytic C(sp3)–C(sp2) Cross-Coupling. ACS Catal. 2016, 6, 873. <https://doi.org/10.1021/acscatal.5b02204>
• Bartling Hanna, Eisenhofer Anna, König Burkhard, Gschwind Ruth M.: The Photocatalyzed Aza-Henry Reaction of N-Aryltetrahydroisoquinolines: Comprehensive Mechanism, H•- versus H+-Abstraction, and Background Reactions. J. Am. Chem. Soc. 2016, 138, 11860. <https://doi.org/10.1021/jacs.6b06658>
• McTiernan C. D., Morin M., McCallum T., Scaiano J. C., Barriault L.: Polynuclear gold(i) complexes in photoredox catalysis: understanding their reactivity through characterization and kinetic analysis. Catal. Sci. Technol. 2016, 6, 201. <https://doi.org/10.1039/C5CY01259G>
• Chen Jun, Cen Jie, Xu Xiaoliang, Li Xiaonian: The application of heterogeneous visible light photocatalysts in organic synthesis. Catal. Sci. Technol. 2016, 6, 349. <https://doi.org/10.1039/C5CY01289A>
• Rackl Daniel, Kreitmeier Peter, Reiser Oliver: Synthesis of a polyisobutylene-tagged fac-Ir(ppy)3 complex and its application as recyclable visible-light photocatalyst in a continuous flow process. Green Chem. 2016, 18, 214. <https://doi.org/10.1039/C5GC01792K>
• Gui Yong-Yuan, Sun Liang, Lu Zhi-Peng, Yu Da-Gang: Photoredox sheds new light on nickel catalysis: from carbon–carbon to carbon–heteroatom bond formation. Org. Chem. Front. 2016, 3, 522. <https://doi.org/10.1039/C5QO00437C>
• Tripathi Shubhangi, Singh Sachchida N., Yadav Lal Dhar S.: Visible light photocatalysis with CBr4: a highly selective aerobic photooxidation of methylarenes to aldehydes. RSC Adv. 2016, 6, 14547. <https://doi.org/10.1039/C5RA26623H>
• Tlahuext-Aca Adrian, Hopkinson Matthew N., Sahoo Basudev, Glorius Frank: Dual gold/photoredox-catalyzed C(sp)–H arylation of terminal alkynes with diazonium salts. Chem. Sci. 2016, 7, 89. <https://doi.org/10.1039/C5SC02583D>
• Ma Jiajia, Harms Klaus, Meggers Eric: Enantioselective rhodium/ruthenium photoredox catalysis en route to chiral 1,2-aminoalcohols. Chem. Commun. 2016, 52, 10183. <https://doi.org/10.1039/C6CC04397F>
• Meyer Andreas Uwe, Berger Anna Lucia, König Burkhard: Metal-free C–H sulfonamidation of pyrroles by visible light photoredox catalysis. Chem. Commun. 2016, 52, 10918. <https://doi.org/10.1039/C6CC06111G>
• Kärkäs Markus D., Åkermark Björn: Water oxidation using earth-abundant transition metal catalysts: opportunities and challenges. Dalton Trans. 2016, 45, 14421. <https://doi.org/10.1039/C6DT00809G>
• Fava Eleonora, Nakajima Masaki, Tabak Martin B., Rueping Magnus: Tin-free visible light photoredox catalysed cyclisation of enamides as a mild procedure for the synthesis of γ-lactams. Green Chem. 2016, 18, 4531. <https://doi.org/10.1039/C6GC01099G>
• Oelgemöller Michael, Hoffmann Norbert: Studies in organic and physical photochemistry – an interdisciplinary approach. Org. Biomol. Chem. 2016, 14, 7392. <https://doi.org/10.1039/C6OB00842A>
• Lévêque Christophe, Chenneberg Ludwig, Corcé Vincent, Goddard Jean-Philippe, Ollivier Cyril, Fensterbank Louis: Primary alkyl bis-catecholato silicates in dual photoredox/nickel catalysis: aryl- and heteroaryl-alkyl cross coupling reactions. Org. Chem. Front. 2016, 3, 462. <https://doi.org/10.1039/C6QO00014B>
• An Yuanyuan, Li Yuewen, Wu Jie: A general route to fluorinated 3,3-disubstituted 2-oxindoles via a photoinduced radical cyclization of N-arylacrylamides under catalyst-free conditions. Org. Chem. Front. 2016, 3, 570. <https://doi.org/10.1039/C6QO00055J>
• Li Yuewen, Zheng Danqing, Li Zhenhua, Wu Jie: Generation of N-aminosulfonamides via a photo-induced fixation of sulfur dioxide into aryl/alkyl halides. Org. Chem. Front. 2016, 3, 574. <https://doi.org/10.1039/C6QO00060F>
• Brahmachari Goutam: Design for carbon–carbon bond forming reactions under ambient conditions. RSC Adv. 2016, 6, 64676. <https://doi.org/10.1039/C6RA14399G>
• Xuan Jun, Zeng Ting‐Ting, Feng Zhu‐Jia, Deng Qiao‐Hui, Chen Jia‐Rong, Lu Liang‐Qiu, Xiao Wen‐Jing, Alper Howard: Redox‐Neutral α‐Allylation of Amines by Combining Palladium Catalysis and Visible‐Light Photoredox Catalysis. Angewandte Chemie 2015, 127, 1645. <https://doi.org/10.1002/ange.201409999>
• Hollister Kyle A., Conner Elizabeth S., Spell Mark L., Deveaux Kristina, Maneval Léa, Beal Michael W., Ragains Justin R.: Remote Hydroxylation through Radical Translocation and Polar Crossover. Angewandte Chemie 2015, 127, 7948. <https://doi.org/10.1002/ange.201500880>
• Iali Wissam, Lanoe Pierre‐Henri, Torelli Stéphane, Jouvenot Damien, Loiseau Frédérique, Lebrun Colette, Hamelin Olivier, Ménage Stéphane: A Ruthenium(II)–Copper(II) Dyad for the Photocatalytic Oxygenation of Organic Substrates Mediated by Dioxygen Activation. Angewandte Chemie 2015, 127, 8535. <https://doi.org/10.1002/ange.201501180>
• Nakajima Masaki, Fava Eleonora, Loescher Sebastian, Jiang Zhen, Rueping Magnus: Eine additivarme photoredoxkatalysierte reduktive Kupplung von Aldehyden, Ketonen und Iminen mit sichtbarem Licht. Angewandte Chemie 2015, 127, 8952. <https://doi.org/10.1002/ange.201501556>
• Sahoo Basudev, Li Jun‐Long, Glorius Frank: Photoredoxkatalysierte Semipinakol‐Umlagerung mit sichtbarem Licht: Trifluormethylierung/Ringerweiterung über einen radikalisch‐polaren Mechanismus. Angewandte Chemie 2015, 127, 11740. <https://doi.org/10.1002/ange.201503210>
• Zhou Quan‐Quan, Guo Wei, Ding Wei, Wu Xiong, Chen Xi, Lu Liang‐Qiu, Xiao Wen‐Jing: Decarboxylative Alkynylation and Carbonylative Alkynylation of Carboxylic Acids Enabled by Visible‐Light Photoredox Catalysis. Angewandte Chemie 2015, 127, 11348. <https://doi.org/10.1002/ange.201504559>
• Corcé Vincent, Chamoreau Lise‐Marie, Derat Etienne, Goddard Jean‐Philippe, Ollivier Cyril, Fensterbank Louis: Silicates as Latent Alkyl Radical Precursors: Visible‐Light Photocatalytic Oxidation of Hypervalent Bis‐Catecholato Silicon Compounds. Angewandte Chemie 2015, 127, 11576. <https://doi.org/10.1002/ange.201504963>
• Xuan Jun, Zhang Zhao‐Guo, Xiao Wen‐Jing: Durch sichtbares Licht induzierte decarboxylierende Funktionalisierung von Carbonsäuren und ihren Derivaten. Angewandte Chemie 2015, 127, 15854. <https://doi.org/10.1002/ange.201505731>
• Tan Yuqi, Yuan Wei, Gong Lei, Meggers Eric: Aerobic Asymmetric Dehydrogenative Cross‐Coupling between Two CH Groups Catalyzed by a Chiral‐at‐Metal Rhodium Complex. Angewandte Chemie 2015, 127, 13237. <https://doi.org/10.1002/ange.201506273>
• Bergonzini Giulia, Cassani Carlo, Wallentin Carl‐Johan: Acyl Radicals from Aromatic Carboxylic Acids by Means of Visible‐Light Photoredox Catalysis. Angewandte Chemie 2015, 127, 14272. <https://doi.org/10.1002/ange.201506432>
• Sahoo Basudev, Hopkinson Matthew N., Glorius Frank: Durch sichtbares Licht vermittelte Synthese von Indolizinen in Abwesenheit eines externen Photokatalysators. Angewandte Chemie 2015, 127, 15766. <https://doi.org/10.1002/ange.201506868>
• Xuan Jun, Zeng Ting‐Ting, Feng Zhu‐Jia, Deng Qiao‐Hui, Chen Jia‐Rong, Lu Liang‐Qiu, Xiao Wen‐Jing, Alper Howard: Redox‐Neutral α‐Allylation of Amines by Combining Palladium Catalysis and Visible‐Light Photoredox Catalysis. Angew Chem Int Ed 2015, 54, 1625. <https://doi.org/10.1002/anie.201409999>
• Hollister Kyle A., Conner Elizabeth S., Spell Mark L., Deveaux Kristina, Maneval Léa, Beal Michael W., Ragains Justin R.: Remote Hydroxylation through Radical Translocation and Polar Crossover. Angew Chem Int Ed 2015, 54, 7837. <https://doi.org/10.1002/anie.201500880>
• Iali Wissam, Lanoe Pierre‐Henri, Torelli Stéphane, Jouvenot Damien, Loiseau Frédérique, Lebrun Colette, Hamelin Olivier, Ménage Stéphane: A Ruthenium(II)–Copper(II) Dyad for the Photocatalytic Oxygenation of Organic Substrates Mediated by Dioxygen Activation. Angew Chem Int Ed 2015, 54, 8415. <https://doi.org/10.1002/anie.201501180>
• Nakajima Masaki, Fava Eleonora, Loescher Sebastian, Jiang Zhen, Rueping Magnus: Photoredox‐Catalyzed Reductive Coupling of Aldehydes, Ketones, and Imines with Visible Light. Angew Chem Int Ed 2015, 54, 8828. <https://doi.org/10.1002/anie.201501556>
• Sahoo Basudev, Li Jun‐Long, Glorius Frank: Visible‐Light Photoredox‐Catalyzed Semipinacol‐Type Rearrangement: Trifluoromethylation/Ring Expansion by a Radical–Polar Mechanism. Angew Chem Int Ed 2015, 54, 11577. <https://doi.org/10.1002/anie.201503210>
• Zhou Quan‐Quan, Guo Wei, Ding Wei, Wu Xiong, Chen Xi, Lu Liang‐Qiu, Xiao Wen‐Jing: Decarboxylative Alkynylation and Carbonylative Alkynylation of Carboxylic Acids Enabled by Visible‐Light Photoredox Catalysis. Angew Chem Int Ed 2015, 54, 11196. <https://doi.org/10.1002/anie.201504559>
• Corcé Vincent, Chamoreau Lise‐Marie, Derat Etienne, Goddard Jean‐Philippe, Ollivier Cyril, Fensterbank Louis: Silicates as Latent Alkyl Radical Precursors: Visible‐Light Photocatalytic Oxidation of Hypervalent Bis‐Catecholato Silicon Compounds. Angew Chem Int Ed 2015, 54, 11414. <https://doi.org/10.1002/anie.201504963>
• Xuan Jun, Zhang Zhao‐Guo, Xiao Wen‐Jing: Visible‐Light‐Induced Decarboxylative Functionalization of Carboxylic Acids and Their Derivatives. Angew Chem Int Ed 2015, 54, 15632. <https://doi.org/10.1002/anie.201505731>
• Tan Yuqi, Yuan Wei, Gong Lei, Meggers Eric: Aerobic Asymmetric Dehydrogenative Cross‐Coupling between Two CH Groups Catalyzed by a Chiral‐at‐Metal Rhodium Complex. Angew Chem Int Ed 2015, 54, 13045. <https://doi.org/10.1002/anie.201506273>
• Bergonzini Giulia, Cassani Carlo, Wallentin Carl‐Johan: Acyl Radicals from Aromatic Carboxylic Acids by Means of Visible‐Light Photoredox Catalysis. Angew Chem Int Ed 2015, 54, 14066. <https://doi.org/10.1002/anie.201506432>
• Sahoo Basudev, Hopkinson Matthew N., Glorius Frank: External‐Photocatalyst‐Free Visible‐Light‐Mediated Synthesis of Indolizines. Angew Chem Int Ed 2015, 54, 15545. <https://doi.org/10.1002/anie.201506868>
• Hoffmann Norbert: Combining Photoredox and Metal Catalysis. ChemCatChem 2015, 7, 393. <https://doi.org/10.1002/cctc.201402868>
• Majek Michal, Filace Fabiana, Jacobi von Wangelin Axel: Visible Light Driven Hydro‐/Deuterodefunctionalization of Anilines. Chemistry A European J 2015, 21, 4518. <https://doi.org/10.1002/chem.201406461>
• Xuan Jun, Zeng Ting‐Ting, Chen Jia‐Rong, Lu Liang‐Qiu, Xiao Wen‐Jing: Room Temperature CP Bond Formation Enabled by Merging Nickel Catalysis and Visible‐Light‐Induced Photoredox Catalysis. Chemistry A European J 2015, 21, 4962. <https://doi.org/10.1002/chem.201500227>
• Holan Martin, Pohl Radek, Císařová Ivana, Klepetářová Blanka, Jones Peter G., Jahn Ullrich: Highly Functionalized Cyclopentane Derivatives by Tandem Michael Addition/Radical Cyclization/Oxygenation Reactions. Chemistry A European J 2015, 21, 9877. <https://doi.org/10.1002/chem.201500424>
• Wang Chengfeng, Ren Xiang, Xie Hujun, Lu Zhan: [3+2] Redox‐Neutral Cycloaddition of Nitrocyclopropanes with Styrenes by Visible‐Light Photocatalysis. Chemistry A European J 2015, 21, 9676. <https://doi.org/10.1002/chem.201500873>
• Wang Chuanyong, Zheng Yu, Huo Haohua, Röse Philipp, Zhang Lilu, Harms Klaus, Hilt Gerhard, Meggers Eric: Merger of Visible Light Induced Oxidation and Enantioselective Alkylation with a Chiral Iridium Catalyst. Chemistry A European J 2015, 21, 7355. <https://doi.org/10.1002/chem.201500998>
• Majek Michal, Faltermeier Uwe, Dick Bernhard, Pérez‐Ruiz Raúl, Jacobi von Wangelin Axel: Application of Visible‐to‐UV Photon Upconversion to Photoredox Catalysis: The Activation of Aryl Bromides. Chemistry A European J 2015, 21, 15496. <https://doi.org/10.1002/chem.201502698>
• Yang Qing‐Qing, Marchini Marianna, Xiao Wen‐Jing, Ceroni Paola, Bandini Marco: Visible‐Light‐Induced Direct Photocatalytic Carboxylation of Indoles with CBr4/MeOH. Chemistry A European J 2015, 21, 18052. <https://doi.org/10.1002/chem.201503787>
• Schneider Ludovic, Mekmouche Yasmina, Rousselot‐Pailley Pierre, Simaan A. Jalila, Robert Viviane, Réglier Marius, Aukauloo Ally, Tron Thierry: Visible‐Light‐Driven Oxidation of Organic Substrates with Dioxygen Mediated by a [Ru(bpy)3]2+/Laccase System. ChemSusChem 2015, 8, 3048. <https://doi.org/10.1002/cssc.201500602>
• Schroll Peter, König Burkhard: Photocatalytic α‐Oxyamination of Stable Enolates, Silyl Enol Ethers, and 2‐Oxoalkane Phosphonic Esters. Eur J Org Chem 2015, 2015, 309. <https://doi.org/10.1002/ejoc.201403433>
• Hoffmann Norbert: Electron and hydrogen transfer in organic photochemical reactions. J of Physical Organic Chem 2015, 28, 121. <https://doi.org/10.1002/poc.3370>
• Xiao Pu, Zhang Jing, Campolo Damien, Dumur Frederic, Gigmes Didier, Fouassier Jean Pierre, Lalevée Jacques: Copper and iron complexes as visible‐light‐sensitive photoinitiators of polymerization. J. Polym. Sci., Part A: Polym. Chem. 2015, 53, 2673. <https://doi.org/10.1002/pola.27762>
• Dong Boliang, Su Yijin, Ye Xiaohan, Petersen Jeffrey L., Shi Xiaodong: Synthesis and characterization of fluorescent-active triazole-gold complexes. Sci. China Chem. 2015, 58, 1235. <https://doi.org/10.1007/s11426-015-5412-z>
• Akita Munetaka, Koike Takashi: Sunlight-driven trifluoromethylation of olefinic substrates by photoredox catalysis: A green organic process. Comptes Rendus Chimie 2015, 18, 742. <https://doi.org/10.1016/j.crci.2015.01.013>
• Zhu Mei, Fu Weijun, Zou Guanglong, Xu Chen, Wang Zhiqiang: Visible-light-mediated radical difluoromethylenephosphonation of 2-isocyanobiaryls with bromodifluoromethylphosphonate for the synthesis of 6-difluoromethylenephosphonyl-phenanthridines. Journal of Fluorine Chemistry 2015, 180, 1. <https://doi.org/10.1016/j.jfluchem.2015.07.028>
• Xiao Pu, Zhang Jing, Dumur Frédéric, Tehfe Mohamad Ali, Morlet-Savary Fabrice, Graff Bernadette, Gigmes Didier, Fouassier Jean Pierre, Lalevée Jacques: Visible light sensitive photoinitiating systems: Recent progress in cationic and radical photopolymerization reactions under soft conditions. Progress in Polymer Science 2015, 41, 32. <https://doi.org/10.1016/j.progpolymsci.2014.09.001>
• Wang Xiaolei, Chen Chuo: An approach for the synthesis of nakamuric acid. Tetrahedron 2015, 71, 3690. <https://doi.org/10.1016/j.tet.2014.10.027>
• Ma Yuyong, De Saptarshi, Chen Chuo: Syntheses of cyclic guanidine-containing natural products. Tetrahedron 2015, 71, 1145. <https://doi.org/10.1016/j.tet.2014.11.056>
• Cao Min-Yi, Ren Xiang, Lu Zhan: Olefin difunctionalizations via visible light photocatalysis. Tetrahedron Letters 2015, 56, 3732. <https://doi.org/10.1016/j.tetlet.2015.04.091>
• Lee Jun Hee, Mho Sun-il: A Tin-Free Route to trans-Diels–Alder Motifs by Visible Light Photoredox Catalysis. J. Org. Chem. 2015, 80, 3309. <https://doi.org/10.1021/acs.joc.5b00041>
• Zheng Lewei, Yang Chao, Xu ZhaoZhong, Gao Fei, Xia Wujiong: Difunctionalization of Alkenes via the Visible-Light-Induced Trifluoromethylarylation/1,4-Aryl Shift/Desulfonylation Cascade Reactions. J. Org. Chem. 2015, 80, 5730. <https://doi.org/10.1021/acs.joc.5b00677>
• Majhi Biju, Kundu Debasish, Ranu Brindaban C.: Ascorbic Acid Promoted Oxidative Arylation of Vinyl Arenes to 2-Aryl Acetophenones without Irradiation at Room Temperature under Aerobic Conditions. J. Org. Chem. 2015, 80, 7739. <https://doi.org/10.1021/acs.joc.5b00825>
• Oderinde Martins S., Varela-Alvarez Adrian, Aquila Brian, Robbins Daniel W., Johannes Jeffrey W.: Effects of Molecular Oxygen, Solvent, and Light on Iridium-Photoredox/Nickel Dual-Catalyzed Cross-Coupling Reactions. J. Org. Chem. 2015, 80, 7642. <https://doi.org/10.1021/acs.joc.5b01193>
• Pratsch Gerald, Overman Larry E.: Synthesis of 2,5-Diaryl-1,5-dienes from Allylic Bromides Using Visible-Light Photoredox Catalysis. J. Org. Chem. 2015, 80, 11388. <https://doi.org/10.1021/acs.joc.5b01962>
• Lu Ping, Hou Tianyuan, Gu Xiangyong, Li Pixu: Visible-Light-Promoted Conversion of Alkyl Benzyl Ether to Alkyl Ester or Alcohol via O-α-sp3 C–H Cleavage. Org. Lett. 2015, 17, 1954. <https://doi.org/10.1021/acs.orglett.5b00663>
• Kaldas Sherif J., Cannillo Alexandre, McCallum Terry, Barriault Louis: Indole Functionalization via Photoredox Gold Catalysis. Org. Lett. 2015, 17, 2864. <https://doi.org/10.1021/acs.orglett.5b01260>
• Zoller Jochen, Fabry David C., Rueping Magnus: Unexpected Dual Role of Titanium Dioxide in the Visible Light Heterogeneous Catalyzed C–H Arylation of Heteroarenes. ACS Catal. 2015, 5, 3900. <https://doi.org/10.1021/acscatal.5b00668>
• Knorn Matthias, Rawner Thomas, Czerwieniec Rafał, Reiser Oliver: [Copper(phenanthroline)(bisisonitrile)]+-Complexes for the Visible-Light-Mediated Atom Transfer Radical Addition and Allylation Reactions. ACS Catal. 2015, 5, 5186. <https://doi.org/10.1021/acscatal.5b01071>
• Huo Haohua, Wang Chuanyong, Harms Klaus, Meggers Eric: Enantioselective, Catalytic Trichloromethylation through Visible-Light-Activated Photoredox Catalysis with a Chiral Iridium Complex. J. Am. Chem. Soc. 2015, 137, 9551. <https://doi.org/10.1021/jacs.5b06010>
• Tang Jian, Grampp Günter, Liu Yun, Wang Bing-Xiang, Tao Fei-Fei, Wang Li-Jun, Liang Xue-Zheng, Xiao Hui-Quan, Shen Yong-Miao: Visible Light Mediated Cyclization of Tertiary Anilines with Maleimides Using Nickel(II) Oxide Surface-Modified Titanium Dioxide Catalyst. J. Org. Chem. 2015, 80, 2724. <https://doi.org/10.1021/jo502901h>
• Meggers Eric: Asymmetric catalysis activated by visible light. Chem. Commun. 2015, 51, 3290. <https://doi.org/10.1039/C4CC09268F>
• Wang Chengfeng, Lu Zhan: Catalytic enantioselective organic transformations via visible light photocatalysis. Org. Chem. Front. 2015, 2, 179. <https://doi.org/10.1039/C4QO00306C>
• Li Yanjie, Miyazawa Kazuki, Koike Takashi, Akita Munetaka: Alkyl- and aryl-thioalkylation of olefins with organotrifluoroborates by photoredox catalysis. Org. Chem. Front. 2015, 2, 319. <https://doi.org/10.1039/C4QO00352G>
• Wu Xinxin, Meng Chunna, Yuan Xiaoqian, Jia Xiaotong, Qian Xuhong, Ye Jinxing: Transition-metal-free visible-light photoredox catalysis at room-temperature for decarboxylative fluorination of aliphatic carboxylic acids by organic dyes. Chem. Commun. 2015, 51, 11864. <https://doi.org/10.1039/C5CC04527D>
• Wang Xiaolei, Gao Yang, Ma Zhiqiang, Rodriguez Rodrigo A., Yu Zhi-Xiang, Chen Chuo: Syntheses of sceptrins and nakamuric acid and insights into the biosyntheses of pyrrole–imidazole dimers. Org. Chem. Front. 2015, 2, 978. <https://doi.org/10.1039/C5QO00165J>
• Dinda Milan, Bose Chandan, Ghosh Tridev, Maity Soumitra: Cross dehydrogenative coupling (CDC) of aldehydes with N-hydroxyimides by visible light photoredox catalysis. RSC Adv. 2015, 5, 44928. <https://doi.org/10.1039/C5RA05719A>
• Dai Xiaojun, Mao Renjie, Guan Baochuan, Xu Xiaoliang, Li Xiaonian: Visible light photoredox catalysis: regioselective radical addition of aminoalkyl radicals to 2,3-allenoates. RSC Adv. 2015, 5, 55290. <https://doi.org/10.1039/C5RA10491B>
• Duret Guillaume, Quinlan Robert, Bisseret Philippe, Blanchard Nicolas: Boron chemistry in a new light. Chem. Sci. 2015, 6, 5366. <https://doi.org/10.1039/C5SC02207J>
• Ravelli Davide, Protti Stefano, Albini Angelo: Energy and Molecules from Photochemical/Photocatalytic Reactions. An Overview. Molecules 2015, 20, 1527. <https://doi.org/10.3390/molecules20011527>
• Schultz Danielle M, Sawicki James W, Yoon Tehshik P: An improved procedure for the preparation of Ru(bpz)3(PF6)2 via a high-yielding synthesis of 2,2’-bipyrazine. Beilstein J. Org. Chem. 2015, 11, 61. <https://doi.org/10.3762/bjoc.11.9>
• Miyake Yoshihiro: Visible-Light-Mediated Transformation of Nitrogen-Containing Compounds Based on Single Electron Transfer. J. Syn. Org. Chem., Jpn. 2015, 73, 874. <https://doi.org/10.5059/yukigoseikyokaishi.73.874>
• Paria Suva, Reiser Oliver: Visible Light Photoredox Catalyzed Cascade Cyclizations of α‐Bromochalcones or α‐Bromocinnamates with Heteroarenes. Adv Synth Catal 2014, 356, 557. <https://doi.org/10.1002/adsc.201301069>
• Guo Wei, Cheng Hong‐Gang, Chen Li‐Yan, Xuan Jun, Feng Zhu‐Jia, Chen Jia‐Rong, Lu Liang‐Qiu, Xiao Wen‐Jing: De Novo Synthesis of γ,γ‐Disubstituted Butyrolactones through a Visible Light Photocatalytic Arylation–Lactonization Sequence. Adv Synth Catal 2014, 356, 2787. <https://doi.org/10.1002/adsc.201400041>
• Pandey Ganesh, Jadhav Deepak, Tiwari Sandip Kumar, Singh Bhawana: Visible Light Photoredox Catalysis: Investigation of Distal sp3 CH Functionalization of Tertiary Amines for Alkylation Reaction. Adv Synth Catal 2014, 356, 2813. <https://doi.org/10.1002/adsc.201400107>
• Xia Xu‐Dong, Xuan Jun, Wang Qiang, Lu Liang‐Qiu, Chen Jia‐Rong, Xiao Wen‐Jing: Synthesis of 2‐Substituted Indoles through Visible Light‐Induced Photocatalytic Cyclizations of Styryl Azides. Adv Synth Catal 2014, 356, 2807. <https://doi.org/10.1002/adsc.201400527>
• Hopkinson Matthew N., Sahoo Basudev, Glorius Frank: Dual Photoredox and Gold Catalysis: Intermolecular Multicomponent Oxyarylation of Alkenes. Adv Synth Catal 2014, 356, 2794. <https://doi.org/10.1002/adsc.201400580>
• Chenneberg Ludwig, Baralle Alexandre, Daniel Marion, Fensterbank Louis, Goddard Jean‐Philippe, Ollivier Cyril: Visible Light Photocatalytic Reduction of O‐Thiocarbamates: Development of a Tin‐Free Barton–McCombie Deoxygenation Reaction. Adv Synth Catal 2014, 356, 2756. <https://doi.org/10.1002/adsc.201400729>
• Liu Jie, Liu Qiang, Yi Hong, Qin Chu, Bai Ruopeng, Qi Xiaotian, Lan Yu, Lei Aiwen: Visible‐Light‐Mediated Decarboxylation/Oxidative Amidation of α‐Keto Acids with Amines under Mild Reaction Conditions Using O2. Angewandte Chemie 2014, 126, 512. <https://doi.org/10.1002/ange.201308614>
• Xuan Jun, Xia Xu‐Dong, Zeng Ting‐Ting, Feng Zhu‐Jia, Chen Jia‐Rong, Lu Liang‐Qiu, Xiao Wen‐Jing: Visible‐Light‐Induced Formal [3+2] Cycloaddition for Pyrrole Synthesis under Metal‐Free Conditions. Angewandte Chemie 2014, 126, 5759. <https://doi.org/10.1002/ange.201400602>
• Kafka František, Holan Martin, Hidasová Denisa, Pohl Radek, Císařová Ivana, Klepetářová Blanka, Jahn Ullrich: Oxidative Katalyse mit dem stöchiometrischen Oxidans als Reagens: eine effiziente Strategie für Einelektronentransfer‐induzierte Anion‐Radikal‐Tandemreaktionen. Angewandte Chemie 2014, 126, 10102. <https://doi.org/10.1002/ange.201403776>
• Hurtley Anna E., Lu Zhan, Yoon Tehshik P.: [2+2] Cycloaddition of 1,3‐Dienes by Visible Light Photocatalysis. Angewandte Chemie 2014, 126, 9137. <https://doi.org/10.1002/ange.201405359>
• Hu Xiao‐Qiang, Chen Jia‐Rong, Wei Qiang, Liu Feng‐Lei, Deng Qiao‐Hui, Beauchemin André M., Xiao Wen‐Jing: Photocatalytic Generation of N‐Centered Hydrazonyl Radicals:  A Strategy for Hydroamination of β,γ‐Unsaturated Hydrazones. Angewandte Chemie 2014, 126, 12359. <https://doi.org/10.1002/ange.201406491>
• Liu Jie, Liu Qiang, Yi Hong, Qin Chu, Bai Ruopeng, Qi Xiaotian, Lan Yu, Lei Aiwen: Visible‐Light‐Mediated Decarboxylation/Oxidative Amidation of α‐Keto Acids with Amines under Mild Reaction Conditions Using O2. Angew Chem Int Ed 2014, 53, 502. <https://doi.org/10.1002/anie.201308614>
• Xuan Jun, Xia Xu‐Dong, Zeng Ting‐Ting, Feng Zhu‐Jia, Chen Jia‐Rong, Lu Liang‐Qiu, Xiao Wen‐Jing: Visible‐Light‐Induced Formal [3+2] Cycloaddition for Pyrrole Synthesis under Metal‐Free Conditions. Angew Chem Int Ed 2014, 53, 5653. <https://doi.org/10.1002/anie.201400602>
• Kafka František, Holan Martin, Hidasová Denisa, Pohl Radek, Císařová Ivana, Klepetářová Blanka, Jahn Ullrich: Oxidative Catalysis Using the Stoichiometric Oxidant as a Reagent: An Efficient Strategy for Single‐Electron‐Transfer‐Induced Tandem Anion–Radical Reactions. Angew Chem Int Ed 2014, 53, 9944. <https://doi.org/10.1002/anie.201403776>
• Hurtley Anna E., Lu Zhan, Yoon Tehshik P.: [2+2] Cycloaddition of 1,3‐Dienes by Visible Light Photocatalysis. Angew Chem Int Ed 2014, 53, 8991. <https://doi.org/10.1002/anie.201405359>
• Hu Xiao‐Qiang, Chen Jia‐Rong, Wei Qiang, Liu Feng‐Lei, Deng Qiao‐Hui, Beauchemin André M., Xiao Wen‐Jing: Photocatalytic Generation of N‐Centered Hydrazonyl Radicals:  A Strategy for Hydroamination of β,γ‐Unsaturated Hydrazones. Angew Chem Int Ed 2014, 53, 12163. <https://doi.org/10.1002/anie.201406491>
• Lawati Haider A. J. Al, Dahmani Zeiyana M. Al, Varma Gouri B, Suliman FakhrEldin O: Photoinduced oxidation of a tris(2,2'‐bipyridyl)ruthenium(II)–peroxodisulfate chemiluminescence system for the analysis of mebeverine HCl pharmaceutical formulations and biological fluids using a two‐chip device. Luminescence 2014, 29, 275. <https://doi.org/10.1002/bio.2540>
• Paria Suva, Reiser Oliver: Copper in Photocatalysis. ChemCatChem 2014, 6, 2477. <https://doi.org/10.1002/cctc.201402237>
• Xue Dong, Jia Zhi‐Hui, Zhao Cong‐Jun, Zhang Yan‐Yan, Wang Chao, Xiao Jianliang: Direct Arylation of N‐Heteroarenes with Aryldiazonium Salts by Photoredox Catalysis in Water. Chemistry A European J 2014, 20, 2960. <https://doi.org/10.1002/chem.201304120>
• Miyake Yoshihiro, Ashida Yuya, Nakajima Kazunari, Nishibayashi Yoshiaki: Visible‐Light‐Mediated Addition of α‐Aminoalkyl Radicals to [60]Fullerene by Using Photoredox Catalysts. Chemistry A European J 2014, 20, 6120. <https://doi.org/10.1002/chem.201304731>
• Hopkinson Matthew N., Sahoo Basudev, Li Jun‐Long, Glorius Frank: Dual Catalysis Sees the Light: Combining Photoredox with Organo‐, Acid, and Transition‐Metal Catalysis. Chemistry A European J 2014, 20, 3874. <https://doi.org/10.1002/chem.201304823>
• Xuan Jun, Feng Zhu‐Jia, Chen Jia‐Rong, Lu Liang‐Qiu, Xiao Wen‐Jing: Visible‐Light‐Induced CS Bond Activation: Facile Access to 1,4‐Diketones from β‐Ketosulfones. Chemistry A European J 2014, 20, 3045. <https://doi.org/10.1002/chem.201304898>
• Su Yuanhai, Straathof Natan J. W., Hessel Volker, Noël Timothy: Photochemical Transformations Accelerated in Continuous‐Flow Reactors: Basic Concepts and Applications. Chemistry A European J 2014, 20, 10562. <https://doi.org/10.1002/chem.201400283>
• Barbante Gregory J., Kebede Noah, Hindson Christopher M., Doeven Egan H., Zammit Elizabeth M., Hanson Graeme R., Hogan Conor F., Francis Paul S.: Control of Excitation and Quenching in Multi‐colour Electrogenerated Chemiluminescence Systems through Choice of Co‐reactant. Chemistry A European J 2014, 20, 14026. <https://doi.org/10.1002/chem.201403767>
• Wang Hao, Tao Jinyi, Cai Xinpei, Chen Wei, Zhao Yueqi, Xu Yang, Yao Wang, Zeng Jing, Wan Qian: Stereoselective Synthesis of α‐Linked 2‐Deoxy Glycosides Enabled by Visible‐Light‐Mediated Reductive Deiodination. Chemistry A European J 2014, 20, 17319. <https://doi.org/10.1002/chem.201405516>
• Liu Yu, Zhang Jia‐Ling, Song Ren‐Jie, Li Jin‐Heng: Visible‐Light‐Facilitated 5‐exo‐trig Cyclization of 1,6‐Dienes with Alkyl Chlorides: Selective Scission of the C(sp3)–H Bond in Alkyl Chlorides. Eur J Org Chem 2014, 2014, 1177. <https://doi.org/10.1002/ejoc.201301849>
• Koike Takashi, Akita Munetaka: Trifluoromethylation by Visible-Light-Driven Photoredox Catalysis. Top Catal 2014, 57, 967. <https://doi.org/10.1007/s11244-014-0259-7>
• Gaikwad A. G.: Modification and application of cellulose fibers for the transport of carbonate ions. Int J Ind Chem 2014, 5. <https://doi.org/10.1007/s40090-014-0012-x>
• Dai Xiao-Jun, Xu Xiao-Liang, Cheng Dong-Ping, Li Xiao-Nian: Visible-light photoredox-mediated oxidation of N-methyl tertiaryamines under catalyst free conditions: Direct synthesis of methylene-bridged bis-1,3-dicarbonyl compounds. Chinese Chemical Letters 2014, 25, 545. <https://doi.org/10.1016/j.cclet.2014.01.021>
• Li Lun, Chen Qing-Yun, Guo Yong: Synthesis of α-CF3 ketones from alkenes and electrophilic trifluoromethylating reagents by visible-light driven photoredox catalysis. Journal of Fluorine Chemistry 2014, 167, 79. <https://doi.org/10.1016/j.jfluchem.2014.05.013>
• Fu Weijun, Zhu Mei, Xu Chen, Zou Guanglong, Wang Zhiqiang, Ji Baoming: Visible-light-mediated trifluoroethylation of 2-isocyanobiaryl with trifluoroethyl iodide: Synthesis of 6-trifluoroethyl-phenanthridines. Journal of Fluorine Chemistry 2014, 168, 50. <https://doi.org/10.1016/j.jfluchem.2014.08.022>
• Hoffmann Norbert: Photochemical reactions applied to the synthesis of helicenes and helicene-like compounds. Journal of Photochemistry and Photobiology C: Photochemistry Reviews 2014, 19, 1. <https://doi.org/10.1016/j.jphotochemrev.2013.11.001>
• Keylor Mitchell H., Park James E., Wallentin Carl-Johan, Stephenson Corey R.J.: Photocatalytic initiation of thiol–ene reactions: synthesis of thiomorpholin-3-ones. Tetrahedron 2014, 70, 4264. <https://doi.org/10.1016/j.tet.2014.03.041>
• Xie Jin, Jin Hongming, Xu Pan, Zhu Chengjian: When C–H bond functionalization meets visible-light photoredox catalysis. Tetrahedron Letters 2014, 55, 36. <https://doi.org/10.1016/j.tetlet.2013.10.090>
• Srivastava Vishnu P., Yadav Arvind K., Yadav Lal Dhar S.: Visible-light-induced cyanation of aza-Baylis–Hillman adducts: a Michael type addition. Tetrahedron Letters 2014, 55, 1788. <https://doi.org/10.1016/j.tetlet.2014.01.121>
• Yadav Arvind K., Yadav Lal Dhar S.: Visible-light-promoted aerobic oxidative cyclization to access 1,3,4-oxadiazoles from aldehydes and acylhydrazides. Tetrahedron Letters 2014, 55, 2065. <https://doi.org/10.1016/j.tetlet.2014.02.022>
• Ding Wei, Zhou Quan-Quan, Xuan Jun, Li Tian-Ren, Lu Liang-Qiu, Xiao Wen-Jing: Photocatalytic aerobic oxidation/semipinacol rearrangement sequence: a concise route to the core of pseudoindoxyl alkaloids. Tetrahedron Letters 2014, 55, 4648. <https://doi.org/10.1016/j.tetlet.2014.06.102>
• Sebren Leanne J., Devery James J., Stephenson Corey R. J.: Catalytic Radical Domino Reactions in Organic Synthesis. ACS Catal. 2014, 4, 703. <https://doi.org/10.1021/cs400995r>
• Li Xiang, Gu Xiangyong, Li Yongjuan, Li Pixu: Aerobic Transition-Metal-Free Visible-Light Photoredox Indole C-3 Formylation Reaction. ACS Catal. 2014, 4, 1897. <https://doi.org/10.1021/cs5005129>
• Rueda-Becerril Montserrat, Mahé Olivier, Drouin Myriam, Majewski Marek B., West Julian G., Wolf Michael O., Sammis Glenn M., Paquin Jean-François: Direct C–F Bond Formation Using Photoredox Catalysis. J. Am. Chem. Soc. 2014, 136, 2637. <https://doi.org/10.1021/ja412083f>
• Shu Xing-zhong, Zhang Miao, He Ying, Frei Heinz, Toste F. Dean: Dual Visible Light Photoredox and Gold-Catalyzed Arylative Ring Expansion. J. Am. Chem. Soc. 2014, 136, 5844. <https://doi.org/10.1021/ja500716j>
• Zuo Zhiwei, MacMillan David W. C.: Decarboxylative Arylation of α-Amino Acids via Photoredox Catalysis: A One-Step Conversion of Biomass to Drug Pharmacophore. J. Am. Chem. Soc. 2014, 136, 5257. <https://doi.org/10.1021/ja501621q>
• Terrett Jack A., Clift Michael D., MacMillan David W. C.: Direct β-Alkylation of Aldehydes via Photoredox Organocatalysis. J. Am. Chem. Soc. 2014, 136, 6858. <https://doi.org/10.1021/ja502639e>
• Tyson Elizabeth L., Niemeyer Zachary L., Yoon Tehshik P.: Redox Mediators in Visible Light Photocatalysis: Photocatalytic Radical Thiol–Ene Additions. J. Org. Chem. 2014, 79, 1427. <https://doi.org/10.1021/jo500031g>
• Dai Xiaojun, Cheng Dongping, Guan Baochuan, Mao Wenjuan, Xu Xiaoliang, Li Xiaonian: The Coupling of Tertiary Amines with Acrylate Derivatives via Visible-Light Photoredox Catalysis. J. Org. Chem. 2014, 79, 7212. <https://doi.org/10.1021/jo501097b>
• Fan Weigang, Yang Qi, Xu Fengshan, Li Pixu: A Visible-Light-Promoted Aerobic Metal-Free C-3 Thiocyanation of Indoles. J. Org. Chem. 2014, 79, 10588. <https://doi.org/10.1021/jo5015799>
• Senthil Murugan Krishnan, Rajendran Thangamuthu, Balakrishnan Gopalakrishnan, Ganesan Muniyandi, Sivasubramanian Veluchamy Kamaraj, Sankar Jeyaraman, Ilangovan Andivelu, Ramamurthy Perumal, Rajagopal Seenivasan: Visible-Light Activation of the Bimetallic Chromophore–Catalyst Dyad: Analysis of Transient Intermediates and Reactivity toward Organic Sulfides. J. Phys. Chem. A 2014, 118, 4451. <https://doi.org/10.1021/jp501084b>
• Oh Se Hwan, Malpani Yashwardhan R., Ha Neul, Jung Young-Sik, Han Soo Bong: Vicinal Difunctionalization of Alkenes: Chlorotrifluoromethylation with CF3SO2Cl by Photoredox Catalysis. Org. Lett. 2014, 16, 1310. <https://doi.org/10.1021/ol403716t>
• Carboni Aude, Dagousset Guillaume, Magnier Emmanuel, Masson Géraldine: Photoredox-Induced Three-Component Oxy-, Amino-, and Carbotrifluoromethylation of Enecarbamates. Org. Lett. 2014, 16, 1240. <https://doi.org/10.1021/ol500374e>
• Hou Hong, Zhu Shaoqun, Pan Fangfang, Rueping Magnus: Visible-Light Photoredox-Catalyzed Synthesis of Nitrones: Unexpected Rate Acceleration by Water in the Synthesis of Isoxazolidines. Org. Lett. 2014, 16, 2872. <https://doi.org/10.1021/ol500893g>
• Dagousset Guillaume, Carboni Aude, Magnier Emmanuel, Masson Géraldine: Photoredox-Induced Three-Component Azido- and Aminotrifluoromethylation of Alkenes. Org. Lett. 2014, 16, 4340. <https://doi.org/10.1021/ol5021477>
• Feng Zhu-Jia, Xuan Jun, Xia Xu-Dong, Ding Wei, Guo Wei, Chen Jia-Rong, Zou You-Quan, Lu Liang-Qiu, Xiao Wen-Jing: Direct sp3 C–H acroleination of N-aryl-tetrahydroisoquinolines by merging photoredox catalysis with nucleophilic catalysis. Org. Biomol. Chem. 2014, 12, 2037. <https://doi.org/10.1039/C3OB42453G>
• Keshari Twinkle, Srivastava Vishnu P., Yadav Lal Dhar S.: Visible-light-initiated photo-oxidative cyclization of phenolic amidines using CBr4 – A metal free approach to 2-aminobenzoxazoles. RSC Adv. 2014, 4, 5815. <https://doi.org/10.1039/c3ra46314a>
• Yadav Arvind K., Srivastava Vishnu P., Yadav Lal Dhar S.: Visible-light-mediated efficient conversion of aldoximes and primary amides into nitriles. RSC Adv. 2014, 4, 4181. <https://doi.org/10.1039/C3RA46553E>
• Bergonzini Giulia, Schindler Corinna S., Wallentin Carl-Johan, Jacobsen Eric N., Stephenson Corey R. J.: Photoredox activation and anion binding catalysis in the dual catalytic enantioselective synthesis of β-amino esters. Chem. Sci. 2014, 5, 112. <https://doi.org/10.1039/C3SC52265B>
• Bergman Nina, Thapper Anders, Styring Stenbjörn, Bergquist Jonas, Shevchenko Denys: Quantitative determination of the Ru(bpy)32+ cation in photochemical reactions by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Anal. Methods 2014, 6, 8513. <https://doi.org/10.1039/C4AY01379D>
• Hari Durga Prasad, König Burkhard: Synthetic applications of eosin Y in photoredox catalysis. Chem. Commun. 2014, 50, 6688. <https://doi.org/10.1039/C4CC00751D>
• Nakajima Masaki, Lefebvre Quentin, Rueping Magnus: Visible light photoredox-catalysed intermolecular radical addition of α-halo amides to olefins. Chem. Commun. 2014, 50, 3619. <https://doi.org/10.1039/c4cc00753k>
• Carboni Aude, Dagousset Guillaume, Magnier Emmanuel, Masson Géraldine: One pot and selective intermolecular aryl- and heteroaryl-trifluoromethylation of alkenes by photoredox catalysis. Chem. Commun. 2014, 50, 14197. <https://doi.org/10.1039/C4CC07066F>
• Zou You-Quan, Guo Wei, Liu Feng-Lei, Lu Liang-Qiu, Chen Jia-Rong, Xiao Wen-Jing: Visible-light-induced photocatalytic formyloxylation reactions of 3-bromooxindoles with water and DMF: the scope and mechanism. Green Chem. 2014, 16, 3787. <https://doi.org/10.1039/C4GC00647J>
• Keshari Twinkle, Yadav Vinod K., Srivastava Vishnu P., Yadav Lal Dhar S.: Visible light organophotoredox catalysis: a general approach to β-keto sulfoxidation of alkenes. Green Chem. 2014, 16, 3986. <https://doi.org/10.1039/C4GC00857J>
• Zhang Cai: Recent advances in trifluoromethylation of organic compounds using Umemoto's reagents. Org. Biomol. Chem. 2014, 12, 6580. <https://doi.org/10.1039/C4OB00671B>
• Koike Takashi, Akita Munetaka: Visible-light radical reaction designed by Ru- and Ir-based photoredox catalysis. Inorg. Chem. Front. 2014, 1, 562. <https://doi.org/10.1039/C4QI00053F>
• Daniel Marion, Fensterbank Louis, Goddard Jean-Philippe, Ollivier Cyril: Visible-light photocatalytic oxidation of 1,3-dicarbonyl compounds and carbon–carbon bond formation. Org. Chem. Front. 2014, 1, 551. <https://doi.org/10.1039/c4qo00071d>
• Liu Yu, Zhang Jia-Ling, Song Ren-Jie, Li Jin-Heng: 1,2-Alkylarylation of activated alkenes with dual C–H bonds of arenes and alkyl halides toward polyhalo-substituted oxindoles. Org. Chem. Front. 2014, 1, 1289. <https://doi.org/10.1039/C4QO00251B>
• Fu Weijun, Zhu Mei, Xu Fengjuan, Fu Yuqin, Xu Chen, Zou Dapeng: An approach to 6-trifluoromethyl-phenanthridines through visible-light-mediated intramolecular radical cyclization of trifluoroacetimidoyl chlorides. RSC Adv. 2014, 4, 17226. <https://doi.org/10.1039/c4ra02384f>
• Yadav Arvind K., Srivastava Vishnu P., Yadav Lal Dhar S.: An easy access to unsymmetrical ureas: a photocatalytic approach to the Lossen rearrangement. RSC Adv. 2014, 4, 24498. <https://doi.org/10.1039/c4ra03805c>
• Credou Julie, Faddoul Rita, Berthelot Thomas: One-step and eco-friendly modification of cellulose membranes by polymer grafting. RSC Adv. 2014, 4, 60959. <https://doi.org/10.1039/C4RA11219A>
• Prier Christopher K., MacMillan David W. C.: Amine α-heteroarylation via photoredox catalysis: a homolytic aromatic substitution pathway. Chem. Sci. 2014, 5, 4173. <https://doi.org/10.1039/C4SC02155J>
• Ghosh Indrajit, Ghosh Tamal, Bardagi Javier I., König Burkhard: Reduction of aryl halides by consecutive visible light-induced electron transfer processes. Science 2014, 346, 725. <https://doi.org/10.1126/science.1258232>
• Tomita Ren, Yasu Yusuke, Koike Takashi, Akita Munetaka: Direct C–H trifluoromethylation of di- and trisubstituted alkenes by photoredox catalysis. Beilstein J. Org. Chem. 2014, 10, 1099. <https://doi.org/10.3762/bjoc.10.108>
• Nguyen Theresa H, Maity Soumitra, Zheng Nan: Visible light mediated intermolecular [3 + 2] annulation of cyclopropylanilines with alkynes. Beilstein J. Org. Chem. 2014, 10, 975. <https://doi.org/10.3762/bjoc.10.96>
• Majek Michal, Filace Fabiana, Wangelin Axel Jacobi von: On the mechanism of photocatalytic reactions with eosin Y. Beilstein J. Org. Chem. 2014, 10, 981. <https://doi.org/10.3762/bjoc.10.97>
• Akita Munetaka, Koike Takashi, Inagaki Akiko: Organometallic Photocatalysis Promoted by Visible Light (Sunlight): Photo-redox Catalysis and Difunctional Dinuclear Catalyst System. J. Synth. Org. Chem. Jpn. 2014, 72, 538. <https://doi.org/10.5059/yukigoseikyokaishi.72.538>
• Zhao Junfeng, Mück‐Lichtenfeld Christian, Studer Armido: Cooperative N‐Heterocyclic Carbene (NHC) and Ruthenium Redox Catalysis: Oxidative Esterification of Aldehydes with Air as the Terminal Oxidant. Adv Synth Catal 2013, 355, 1098. <https://doi.org/10.1002/adsc.201300034>
• Donck Simon, Baroudi Abdulkader, Fensterbank Louis, Goddard Jean‐Philippe, Ollivier Cyril: Visible‐Light Photocatalytic Reduction of Sulfonium Salts as a Source of Aryl Radicals. Adv Synth Catal 2013, 355, 1477. <https://doi.org/10.1002/adsc.201300040>
• An Jing, Zou You‐Quan, Yang Qing‐Qing, Wang Qiang, Xiao Wen‐Jing: Visible Light‐Induced Aerobic Oxyamidation of Indoles: A Photocatalytic Strategy for the Preparation of Tetrahydro‐5H‐indolo[2,3‐b]quinolinols. Adv Synth Catal 2013, 355, 1483. <https://doi.org/10.1002/adsc.201300175>
• Kachkovskyi Georgiy, Faderl Christian, Reiser Oliver: Visible Light‐Mediated Synthesis of (Spiro)anellated Furans. Adv Synth Catal 2013, 355, 2240. <https://doi.org/10.1002/adsc.201300221>
• Deng Guo‐Bo, Wang Zhi‐Qiang, Xia Jia‐Dong, Qian Peng‐Cheng, Song Ren‐Jie, Hu Ming, Gong Lu‐Bin, Li Jin‐Heng: Tandem Cyclizations of 1,6‐Enynes with Arylsulfonyl Chlorides by Using Visible‐Light Photoredox Catalysis. Angewandte Chemie 2013, 125, 1575. <https://doi.org/10.1002/ange.201208380>
• Hari Durga Prasad, König Burkhard: Die photokatalytische Meerwein‐Arylierung: eine klassische Aryldiazoniumsalz‐Reaktion in neuem Licht. Angewandte Chemie 2013, 125, 4832. <https://doi.org/10.1002/ange.201210276>
• Majek Michal, Jacobi von Wangelin Axel: Lichtvermittelte kupferkatalysierte C‐C‐ und C‐N‐Bindungsknüpfung. Angewandte Chemie 2013, 125, 6033. <https://doi.org/10.1002/ange.201301843>
• Revol Guillaume, McCallum Terry, Morin Mathieu, Gagosz Fabien, Barriault Louis: Photoredox Transformations with Dimeric Gold Complexes. Angewandte Chemie 2013, 125, 13584. <https://doi.org/10.1002/ange.201306727>
• Deng Guo‐Bo, Wang Zhi‐Qiang, Xia Jia‐Dong, Qian Peng‐Cheng, Song Ren‐Jie, Hu Ming, Gong Lu‐Bin, Li Jin‐Heng: Tandem Cyclizations of 1,6‐Enynes with Arylsulfonyl Chlorides by Using Visible‐Light Photoredox Catalysis. Angew Chem Int Ed 2013, 52, 1535. <https://doi.org/10.1002/anie.201208380>
• Hari Durga Prasad, König Burkhard: The Photocatalyzed Meerwein Arylation: Classic Reaction of Aryl Diazonium Salts in a New Light. Angew Chem Int Ed 2013, 52, 4734. <https://doi.org/10.1002/anie.201210276>
• Majek Michal, Jacobi von Wangelin Axel: Ambient‐Light‐Mediated Copper‐Catalyzed CC and CN Bond Formation. Angew Chem Int Ed 2013, 52, 5919. <https://doi.org/10.1002/anie.201301843>
• Revol Guillaume, McCallum Terry, Morin Mathieu, Gagosz Fabien, Barriault Louis: Photoredox Transformations with Dimeric Gold Complexes. Angew Chem Int Ed 2013, 52, 13342. <https://doi.org/10.1002/anie.201306727>
• Xuan Jun, Li Bin‐Jie, Feng Zhu‐Jia, Sun Guo‐Dong, Ma Huan‐Huan, Yuan Zhi‐Wei, Chen Jia‐Rong, Lu Liang‐Qiu, Xiao Wen‐Jing: Desulfonylation of Tosyl Amides through Catalytic Photoredox Cleavage of NS Bond Under Visible‐Light Irradiation. Chemistry — An Asian Journal 2013, 8, 1090. <https://doi.org/10.1002/asia.201300224>
• Liu Qiang, Yi Hong, Liu Jie, Yang Yuhong, Zhang Xu, Zeng Ziqi, Lei Aiwen: Visible‐Light Photocatalytic Radical Alkenylation of α‐Carbonyl Alkyl Bromides and Benzyl Bromides. Chemistry A European J 2013, 19, 5120. <https://doi.org/10.1002/chem.201203694>
• Baralle Alexandre, Fensterbank Louis, Goddard Jean‐Philippe, Ollivier Cyril: Aryl Radical Formation by Copper(I) Photocatalyzed Reduction of Diaryliodonium Salts: NMR Evidence for a CuII/CuI Mechanism. Chemistry A European J 2013, 19, 10809. <https://doi.org/10.1002/chem.201301449>
• Gu Xiangyong, Li Xiang, Qu Yue, Yang Qi, Li Pixu, Yao Yingming: Intermolecular Visible‐Light Photoredox Atom‐Transfer Radical [3+2]‐Cyclization of 2‐(Iodomethyl)cyclopropane‐1,1‐dicarboxylate with Alkenes and Alkynes. Chemistry A European J 2013, 19, 11878. <https://doi.org/10.1002/chem.201301943>
• Xu Pan, Xie Jin, Xue Qicai, Pan Changduo, Cheng Yixiang, Zhu Chengjian: Visible‐Light‐Induced Trifluoromethylation of N‐Aryl Acrylamides: A Convenient and Effective Method To Synthesize CF3‐Containing Oxindoles Bearing a Quaternary Carbon Center. Chemistry A European J 2013, 19, 14039. <https://doi.org/10.1002/chem.201302407>
• Xuan Jun, Lu Liang‐Qiu, Chen Jia‐Rong, Xiao Wen‐Jing: Visible‐Light‐Driven Photoredox Catalysis in the Construction of Carbocyclic and Heterocyclic Ring Systems. Eur J Org Chem 2013, 2013, 6755. <https://doi.org/10.1002/ejoc.201300596>
• Zibareva I. V., Parmon V. N.: Identification of “hot spots” of the science of catalysis: bibliometric and thematic analysis of nowaday reviews and monographs. Russ Chem Bull 2013, 62, 2266. <https://doi.org/10.1007/s11172-013-0329-1>
• Spell Mark, Wang Xiaoping, Wahba Amir E., Conner Elizabeth, Ragains Justin: An α-selective, visible light photocatalytic glycosylation of alcohols with selenoglycosides. Carbohydrate Research 2013, 369, 42. <https://doi.org/10.1016/j.carres.2013.01.004>
• Mizuta Satoshi, Verhoog Stefan, Wang Xin, Shibata Norio, Gouverneur Véronique, Médebielle Maurice: Redox chemistry of trifluoromethyl sulfonium salts as CF3 radical sources. Journal of Fluorine Chemistry 2013, 155, 124. <https://doi.org/10.1016/j.jfluchem.2013.07.006>
• Zhao Yaohong, Cai Shunyou, Li Jing, Wang David Zhigang: Visible-light photo-catalytic C–C bond cleavages: preparations of N,N-dialkylformamides from 1,2-vicinal diamines. Tetrahedron 2013, 69, 8129. <https://doi.org/10.1016/j.tet.2013.07.056>
• Bouriga Meriem, Chehimi Mohamed M., Combellas Catherine, Decorse Philippe, Kanoufi Frédéric, Deronzier Alain, Pinson Jean: Sensitized Photografting of Diazonium Salts by Visible Light. Chem. Mater. 2013, 25, 90. <https://doi.org/10.1021/cm3032994>
• Prier Christopher K., Rankic Danica A., MacMillan David W. C.: Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis. Chem. Rev. 2013, 113, 5322. <https://doi.org/10.1021/cr300503r>
• Yoon Tehshik P.: Visible Light Photocatalysis: The Development of Photocatalytic Radical Ion Cycloadditions. ACS Catal. 2013, 3, 895. <https://doi.org/10.1021/cs400088e>
• Rueping Magnus, Vila Carlos, Bootwicha Teerawut: Continuous Flow Organocatalytic C–H Functionalization and Cross-Dehydrogenative Coupling Reactions: Visible Light Organophotocatalysis for Multicomponent Reactions and C–C, C–P Bond Formations. ACS Catal. 2013, 3, 1676. <https://doi.org/10.1021/cs400350j>
• Zhu Shaoqun, Das Arindam, Bui Lan, Zhou Hanjun, Curran Dennis P., Rueping Magnus: Oxygen Switch in Visible-Light Photoredox Catalysis: Radical Additions and Cyclizations and Unexpected C–C-Bond Cleavage Reactions. J. Am. Chem. Soc. 2013, 135, 1823. <https://doi.org/10.1021/ja309580a>
• Sahoo Basudev, Hopkinson Matthew N., Glorius Frank: Combining Gold and Photoredox Catalysis: Visible Light-Mediated Oxy- and Aminoarylation of Alkenes. J. Am. Chem. Soc. 2013, 135, 5505. <https://doi.org/10.1021/ja400311h>
• Mizuta Satoshi, Verhoog Stefan, Engle Keary M., Khotavivattana Tanatorn, O’Duill Miriam, Wheelhouse Katherine, Rassias Gerasimos, Médebielle Maurice, Gouverneur Véronique: Catalytic Hydrotrifluoromethylation of Unactivated Alkenes. J. Am. Chem. Soc. 2013, 135, 2505. <https://doi.org/10.1021/ja401022x>
• Rono Lydia J., Yayla Hatice G., Wang David Y., Armstrong Michael F., Knowles Robert R.: Enantioselective Photoredox Catalysis Enabled by Proton-Coupled Electron Transfer: Development of an Asymmetric Aza-Pinacol Cyclization. J. Am. Chem. Soc. 2013, 135, 17735. <https://doi.org/10.1021/ja4100595>
• Tyson Elizabeth L., Ament Michael S., Yoon Tehshik P.: Transition Metal Photoredox Catalysis of Radical Thiol-Ene Reactions. J. Org. Chem. 2013, 78, 2046. <https://doi.org/10.1021/jo3020825>
• Ruiz Espelt Laura, Wiensch Eric M., Yoon Tehshik P.: Brønsted Acid Cocatalysts in Photocatalytic Radical Addition of α-Amino C–H Bonds across Michael Acceptors. J. Org. Chem. 2013, 78, 4107. <https://doi.org/10.1021/jo400428m>
• Wever Walter J., Cinelli Maris A., Bowers Albert A.: Visible Light Mediated Activation and O-Glycosylation of Thioglycosides. Org. Lett. 2013, 15, 30. <https://doi.org/10.1021/ol302941q>
• Sun Hongnan, Yang Chao, Gao Fei, Li Zhe, Xia Wujiong: Oxidative C–C Bond Cleavage of Aldehydes via Visible-Light Photoredox Catalysis. Org. Lett. 2013, 15, 624. <https://doi.org/10.1021/ol303437m>
• Mizuta Satoshi, Engle Keary M., Verhoog Stefan, Galicia-López Oscar, O’Duill Miriam, Médebielle Maurice, Wheelhouse Katherine, Rassias Gerasimos, Thompson Amber L., Gouverneur Véronique: Trifluoromethylation of Allylsilanes under Photoredox Catalysis. Org. Lett. 2013, 15, 1250. <https://doi.org/10.1021/ol400184t>
• Rueping Magnus, Vila Carlos: Visible Light Photoredox-Catalyzed Multicomponent Reactions. Org. Lett. 2013, 15, 2092. <https://doi.org/10.1021/ol400317v>
• Yasu Yusuke, Koike Takashi, Akita Munetaka: Intermolecular Aminotrifluoromethylation of Alkenes by Visible-Light-Driven Photoredox Catalysis. Org. Lett. 2013, 15, 2136. <https://doi.org/10.1021/ol4006272>
• Zhou Hongxia, Lu Ping, Gu Xiangyong, Li Pixu: Visible-Light-Mediated Nucleophilic Addition of an α-Aminoalkyl Radical to Isocyanate or Isothiocyanate. Org. Lett. 2013, 15, 5646. <https://doi.org/10.1021/ol402573j>
• Nguyen John D., Reiß Barbara, Dai Chunhui, Stephenson Corey R. J.: Batch to flow deoxygenation using visible light photoredox catalysis. Chem. Commun. 2013, 49, 4352. <https://doi.org/10.1039/C2CC37206A>
• Ravelli Davide, Fagnoni Maurizio, Albini Angelo: Photoorganocatalysis. What for?. Chem. Soc. Rev. 2013, 42, 97. <https://doi.org/10.1039/C2CS35250H>
• Gu Xiangyong, Li Xiang, Chai Yahong, Yang Qi, Li Pixu, Yao Yingming: A simple metal-free catalytic sulfoxidation under visible light and air. Green Chem. 2013, 15, 357. <https://doi.org/10.1039/c2gc36683e>
• Yasu Yusuke, Koike Takashi, Akita Munetaka: Visible-light-induced synthesis of a variety of trifluoromethylated alkenes from potassium vinyltrifluoroborates by photoredox catalysis. Chem. Commun. 2013, 49, 2037. <https://doi.org/10.1039/c3cc39235j>
• Majek Michal, von Wangelin Axel Jacobi: Organocatalytic visible light mediated synthesis of aryl sulfides. Chem. Commun. 2013, 49, 5507. <https://doi.org/10.1039/c3cc41867g>
• Xie Jin, Xu Pan, Li Huamin, Xue Qicai, Jin Hongming, Cheng Yixiang, Zhu Chengjian: A room temperature decarboxylation/C–H functionalization cascade by visible-light photoredox catalysis. Chem. Commun. 2013, 49, 5672. <https://doi.org/10.1039/c3cc42672f>
• Miyazawa Kazuki, Yasu Yusuke, Koike Takashi, Akita Munetaka: Visible-light-induced hydroalkoxymethylation of electron-deficient alkenes by photoredox catalysis. Chem. Commun. 2013, 49, 7249. <https://doi.org/10.1039/c3cc42695e>
• Yadav Arvind K., Srivastava Vishnu P., Yadav Lal Dhar S.: Visible-light-mediated eosin Y catalyzed aerobic desulfurization of thioamides into amides. New J. Chem. 2013, 37, 4119. <https://doi.org/10.1039/c3nj00870c>
• Xi Yumeng, Yi Hong, Lei Aiwen: Synthetic applications of photoredox catalysis with visible light. Org. Biomol. Chem. 2013, 11, 2387. <https://doi.org/10.1039/c3ob40137e>
• Gu Xiangyong, Lu Ping, Fan Weigang, Li Pixu, Yao Yingming: Visible light photoredox atom transfer Ueno–Stork reaction. Org. Biomol. Chem. 2013, 11, 7088. <https://doi.org/10.1039/c3ob41600c>
• Pirnot Michael T., Rankic Danica A., Martin David B. C., MacMillan David W. C.: Photoredox Activation for the Direct β-Arylation of Ketones and Aldehydes. Science 2013, 339, 1593. <https://doi.org/10.1126/science.1232993>
• Hu Jie, Wang Jiang, Nguyen Theresa H, Zheng Nan: The chemistry of amine radical cations produced by visible light photoredox catalysis. Beilstein J. Org. Chem. 2013, 9, 1977. <https://doi.org/10.3762/bjoc.9.234>
• Yu Jian, Zhang Ling, Yan Guobing: Metal‐Free, Visible Light‐Induced Borylation of Aryldiazonium Salts: A Simple and Green Synthetic Route to Arylboronates. Adv Synth Catal 2012, 354, 2625. <https://doi.org/10.1002/adsc.201200416>
• Xiao Tiebo, Dong Xichang, Tang Yanchi, Zhou Lei: Phenanthrene Synthesis by Eosin Y‐Catalyzed, Visible Light‐ Induced [4+2] Benzannulation of Biaryldiazonium Salts with Alkynes. Adv Synth Catal 2012, 354, 3195. <https://doi.org/10.1002/adsc.201200569>
• Yasu Yusuke, Koike Takashi, Akita Munetaka: Visible Light‐Induced Selective Generation of Radicals from Organoborates by Photoredox Catalysis. Adv Synth Catal 2012, 354, 3414. <https://doi.org/10.1002/adsc.201200588>
• Cherevatskaya Maria, Neumann Matthias, Füldner Stefan, Harlander Christoph, Kümmel Susanne, Dankesreiter Stephan, Pfitzner Arno, Zeitler Kirsten, König Burkhard: Stereoselektive Alkylierung mit sichtbarem Licht durch Kombination von heterogener Photokatalyse mit Organokatalyse. Angewandte Chemie 2012, 124, 4138. <https://doi.org/10.1002/ange.201108721>
• Xuan Jun, Xiao Wen‐Jing: Photoredoxkatalyse mit sichtbarem Licht. Angewandte Chemie 2012, 124, 6934. <https://doi.org/10.1002/ange.201200223>
• Andrews R. Stephen, Becker Jennifer J., Gagné Michel R.: A Photoflow Reactor for the Continuous Photoredox‐Mediated Synthesis of C‐Glycoamino Acids and C‐Glycolipids. Angewandte Chemie 2012, 124, 4216. <https://doi.org/10.1002/ange.201200593>
• Tucker Joseph W., Zhang Yuan, Jamison Timothy F., Stephenson Corey R. J.: Visible‐Light Photoredox Catalysis in Flow. Angewandte Chemie 2012, 124, 4220. <https://doi.org/10.1002/ange.201200961>
• Cai Shunyou, Zhao Xinyang, Wang Xinbo, Liu Qisong, Li Zigang, Wang David Zhigang: Visible‐Light‐Promoted CC Bond Cleavage: Photocatalytic Generation of Iminium Ions and Amino Radicals. Angewandte Chemie 2012, 124, 8174. <https://doi.org/10.1002/ange.201202880>
• Kim Hyejin, Lee Chulbom: Visible‐Light‐Induced Photocatalytic Reductive Transformations of Organohalides. Angewandte Chemie 2012, 124, 12469. <https://doi.org/10.1002/ange.201203599>
• Lu Zhan, Yoon Tehshik P.: Visible Light Photocatalysis of [2+2] Styrene Cycloadditions by Energy Transfer. Angewandte Chemie 2012, 124, 10475. <https://doi.org/10.1002/ange.201204835>
• Schnermann Martin J., Overman Larry E.: A Concise Synthesis of (−)‐Aplyviolene Facilitated by a Strategic Tertiary Radical Conjugate Addition. Angewandte Chemie 2012, 124, 9714. <https://doi.org/10.1002/ange.201204977>
• Yasu Yusuke, Koike Takashi, Akita Munetaka: Three‐component Oxytrifluoromethylation of Alkenes: Highly Efficient and Regioselective Difunctionalization of CC Bonds Mediated by Photoredox Catalysts. Angewandte Chemie 2012, 124, 9705. <https://doi.org/10.1002/ange.201205071>
• Maity Soumitra, Zheng Nan: A Visible‐Light‐Mediated Oxidative CN Bond Formation/Aromatization Cascade: Photocatalytic Preparation of N‐Arylindoles. Angewandte Chemie 2012, 124, 9700. <https://doi.org/10.1002/ange.201205137>
• Cherevatskaya Maria, Neumann Matthias, Füldner Stefan, Harlander Christoph, Kümmel Susanne, Dankesreiter Stephan, Pfitzner Arno, Zeitler Kirsten, König Burkhard: Visible‐Light‐Promoted Stereoselective Alkylation by Combining Heterogeneous Photocatalysis with Organocatalysis. Angew Chem Int Ed 2012, 51, 4062. <https://doi.org/10.1002/anie.201108721>
• Xuan Jun, Xiao Wen‐Jing: Visible‐Light Photoredox Catalysis. Angew Chem Int Ed 2012, 51, 6828. <https://doi.org/10.1002/anie.201200223>
• Andrews R. Stephen, Becker Jennifer J., Gagné Michel R.: A Photoflow Reactor for the Continuous Photoredox‐Mediated Synthesis of C‐Glycoamino Acids and C‐Glycolipids. Angew Chem Int Ed 2012, 51, 4140. <https://doi.org/10.1002/anie.201200593>
• Tucker Joseph W., Zhang Yuan, Jamison Timothy F., Stephenson Corey R. J.: Visible‐Light Photoredox Catalysis in Flow. Angew Chem Int Ed 2012, 51, 4144. <https://doi.org/10.1002/anie.201200961>
• Cai Shunyou, Zhao Xinyang, Wang Xinbo, Liu Qisong, Li Zigang, Wang David Zhigang: Visible‐Light‐Promoted CC Bond Cleavage: Photocatalytic Generation of Iminium Ions and Amino Radicals. Angew Chem Int Ed 2012, 51, 8050. <https://doi.org/10.1002/anie.201202880>
• Kim Hyejin, Lee Chulbom: Visible‐Light‐Induced Photocatalytic Reductive Transformations of Organohalides. Angew Chem Int Ed 2012, 51, 12303. <https://doi.org/10.1002/anie.201203599>
• Lu Zhan, Yoon Tehshik P.: Visible Light Photocatalysis of [2+2] Styrene Cycloadditions by Energy Transfer. Angew Chem Int Ed 2012, 51, 10329. <https://doi.org/10.1002/anie.201204835>
• Schnermann Martin J., Overman Larry E.: A Concise Synthesis of (−)‐Aplyviolene Facilitated by a Strategic Tertiary Radical Conjugate Addition. Angew Chem Int Ed 2012, 51, 9576. <https://doi.org/10.1002/anie.201204977>
• Yasu Yusuke, Koike Takashi, Akita Munetaka: Three‐component Oxytrifluoromethylation of Alkenes: Highly Efficient and Regioselective Difunctionalization of CC Bonds Mediated by Photoredox Catalysts. Angew Chem Int Ed 2012, 51, 9567. <https://doi.org/10.1002/anie.201205071>
• Maity Soumitra, Zheng Nan: A Visible‐Light‐Mediated Oxidative CN Bond Formation/Aromatization Cascade: Photocatalytic Preparation of N‐Arylindoles. Angew Chem Int Ed 2012, 51, 9562. <https://doi.org/10.1002/anie.201205137>
• Courant Thibaut, Masson Géraldine: Photoredox‐Initiated α‐Alkylation of Imines through a Three‐Component Radical/Cationic Reaction. Chemistry A European J 2012, 18, 423. <https://doi.org/10.1002/chem.201103062>
• Rueping Magnus, Zoller Jochen, Fabry David C., Poscharny Konstantin, Koenigs René M., Weirich Thomas E., Mayer Joachim: Light‐Mediated Heterogeneous Cross Dehydrogenative Coupling Reactions: Metal Oxides as Efficient, Recyclable, Photoredox Catalysts in CC Bond‐Forming Reactions. Chemistry A European J 2012, 18, 3478. <https://doi.org/10.1002/chem.201103242>
• Rueping Magnus, Koenigs René M., Poscharny Konstantin, Fabry David C., Leonori Daniele, Vila Carlos: Dual Catalysis: Combination of Photocatalytic Aerobic Oxidation and Metal Catalyzed Alkynylation Reactions—CC Bond Formation Using Visible Light. Chemistry A European J 2012, 18, 5170. <https://doi.org/10.1002/chem.201200050>
• Pirtsch Michael, Paria Suva, Matsuno Taisuke, Isobe Hiroyuki, Reiser Oliver: [Cu(dap)2Cl] As an Efficient Visible‐Light‐Driven Photoredox Catalyst in Carbon–Carbon Bond‐Forming Reactions. Chemistry A European J 2012, 18, 7336. <https://doi.org/10.1002/chem.201200967>
• Miyake Yoshihiro, Nakajima Kazunari, Nishibayashi Yoshiaki: Direct sp3 CH Amination of Nitrogen‐Containing Benzoheterocycles Mediated by Visible‐Light‐Photoredox Catalysts. Chemistry A European J 2012, 18, 16473. <https://doi.org/10.1002/chem.201203066>
• Hoffmann Norbert: Homogeneous Photocatalytic Reactions with Organometallic and Coordination Compounds—Perspectives for Sustainable Chemistry. ChemSusChem 2012, 5, 352. <https://doi.org/10.1002/cssc.201100286>
• Schroll Peter, Hari Durga Prasad, König Burkhard: Photocatalytic Arylation of Alkenes, Alkynes and Enones with Diazonium Salts. ChemistryOpen 2012, 1, 130. <https://doi.org/10.1002/open.201200011>
• Hamdy Mohamed S., Scott Elinor L., Carr Robert H., Sanders Johan P. M.: A Novel Photocatalytic Conversion of Tryptophan to Kynurenine Using Black Light as a Light Source. Catal Lett 2012, 142, 338. <https://doi.org/10.1007/s10562-012-0775-7>
• Zou You-Quan, Duan Shu-Wen, Meng Xiang-Gao, Hu Xiao-Qiang, Gao Shuang, Chen Jia-Rong, Xiao Wen-Jing: Visible light induced intermolecular [2+2]-cycloaddition reactions of 3-ylideneoxindoles through energy transfer pathway. Tetrahedron 2012, 68, 6914. <https://doi.org/10.1016/j.tet.2012.06.011>
• Lin Shishi, Padilla Christian E., Ischay Michael A., Yoon Tehshik P.: Visible light photocatalysis of intramolecular radical cation Diels–Alder cycloadditions. Tetrahedron Letters 2012, 53, 3073. <https://doi.org/10.1016/j.tetlet.2012.04.021>
• Rueping Magnus, Vila Carlos, Szadkowska Anna, Koenigs Rene M., Fronert Jeanne: Photoredox Catalysis as an Efficient Tool for the Aerobic Oxidation of Amines and Alcohols: Bioinspired Demethylations and Condensations. ACS Catal. 2012, 2, 2810. <https://doi.org/10.1021/cs300604k>
• Guillo Pascal, Hamelin Olivier, Batat Pinar, Jonusauskas Gediminas, McClenaghan Nathan D., Ménage Stéphane: Photocatalyzed Sulfide Oxygenation with Water as the Unique Oxygen Atom Source. Inorg. Chem. 2012, 51, 2222. <https://doi.org/10.1021/ic2022159>
• Miyake Yoshihiro, Nakajima Kazunari, Nishibayashi Yoshiaki: Visible-Light-Mediated Utilization of α-Aminoalkyl Radicals: Addition to Electron-Deficient Alkenes Using Photoredox Catalysts. J. Am. Chem. Soc. 2012, 134, 3338. <https://doi.org/10.1021/ja211770y>
• Hari Durga Prasad, Schroll Peter, König Burkhard: Metal-Free, Visible-Light-Mediated Direct C–H Arylation of Heteroarenes with Aryl Diazonium Salts. J. Am. Chem. Soc. 2012, 134, 2958. <https://doi.org/10.1021/ja212099r>
• Wallentin Carl-Johan, Nguyen John D., Finkbeiner Peter, Stephenson Corey R. J.: Visible Light-Mediated Atom Transfer Radical Addition via Oxidative and Reductive Quenching of Photocatalysts. J. Am. Chem. Soc. 2012, 134, 8875. <https://doi.org/10.1021/ja300798k>
• Tucker Joseph W., Stephenson Corey R. J.: Shining Light on Photoredox Catalysis: Theory and Synthetic Applications. J. Org. Chem. 2012, 77, 1617. <https://doi.org/10.1021/jo202538x>
• Dai Chunhui, Meschini Francesco, Narayanam Jagan M. R., Stephenson Corey R. J.: Friedel–Crafts Amidoalkylation via Thermolysis and Oxidative Photocatalysis. J. Org. Chem. 2012, 77, 4425. <https://doi.org/10.1021/jo300162c>
• Zhao Guolei, Yang Chao, Guo Lin, Sun Hongnan, Lin Run, Xia Wujiong: Reactivity Insight into Reductive Coupling and Aldol Cyclization of Chalcones by Visible Light Photocatalysis. J. Org. Chem. 2012, 77, 6302. <https://doi.org/10.1021/jo300796j>
• Wang Zhi-Qiang, Hu Ming, Huang Xiao-Cheng, Gong Lu-Bing, Xie Ye-Xiang, Li Jin-Heng: Direct α-Arylation of α-Amino Carbonyl Compounds with Indoles Using Visible Light Photoredox Catalysis. J. Org. Chem. 2012, 77, 8705. <https://doi.org/10.1021/jo301691h>
• Hering Thea, Hari Durga Prasad, König Burkhard: Visible-Light-Mediated α-Arylation of Enol Acetates Using Aryl Diazonium Salts. J. Org. Chem. 2012, 77, 10347. <https://doi.org/10.1021/jo301984p>
• Kohls Paul, Jadhav Deepak, Pandey Ganesh, Reiser Oliver: Visible Light Photoredox Catalysis: Generation and Addition of N-Aryltetrahydroisoquinoline-Derived α-Amino Radicals to Michael Acceptors. Org. Lett. 2012, 14, 672. <https://doi.org/10.1021/ol202857t>
• Freeman David B., Furst Laura, Condie Allison G., Stephenson Corey R. J.: Functionally Diverse Nucleophilic Trapping of Iminium Intermediates Generated Utilizing Visible Light. Org. Lett. 2012, 14, 94. <https://doi.org/10.1021/ol202883v>
• Cheng Yannan, Yang Jun, Qu Yue, Li Pixu: Aerobic Visible-Light Photoredox Radical C–H Functionalization: Catalytic Synthesis of 2-Substituted Benzothiazoles. Org. Lett. 2012, 14, 98. <https://doi.org/10.1021/ol2028866>
• Tyson Elizabeth L., Farney Elliot P., Yoon Tehshik P.: Photocatalytic [2 + 2] Cycloadditions of Enones with Cleavable Redox Auxiliaries. Org. Lett. 2012, 14, 1110. <https://doi.org/10.1021/ol3000298>
• Parrish Jonathan D., Ischay Michael A., Lu Zhan, Guo Song, Peters Noël R., Yoon Tehshik P.: Endoperoxide Synthesis by Photocatalytic Aerobic [2 + 2 + 2] Cycloadditions. Org. Lett. 2012, 14, 1640. <https://doi.org/10.1021/ol300428q>
• Neumann Matthias, Zeitler Kirsten: Application of Microflow Conditions to Visible Light Photoredox Catalysis. Org. Lett. 2012, 14, 2658. <https://doi.org/10.1021/ol3005529>
• Yoon Hyo-Sang, Ho Xuan-Huong, Jang Jiyeon, Lee Hwa-Jung, Kim Seung-Joo, Jang Hye-Young: N719 Dye-Sensitized Organophotocatalysis: Enantioselective Tandem Michael Addition/Oxyamination of Aldehydes. Org. Lett. 2012, 14, 3272. <https://doi.org/10.1021/ol3011858>
• Hari Durga Prasad, Hering Thea, König Burkhard: Visible Light Photocatalytic Synthesis of Benzothiophenes. Org. Lett. 2012, 14, 5334. <https://doi.org/10.1021/ol302517n>
• Zhao Guolei, Yang Chao, Guo Lin, Sun Hongnan, Chen Chao, Xia Wujiong: Visible light-induced oxidative coupling reaction: easy access to Mannich-type products. Chem Commn 2012, 48, 2337. <https://doi.org/10.1039/c2cc17130a>
• Yasu Yusuke, Koike Takashi, Akita Munetaka: Sunlight-driven synthesis of γ-diketones via oxidative coupling of enamines with silyl enol ethers catalyzed by [Ru(bpy)3]2+. Chem Commn 2012, 48, 5355. <https://doi.org/10.1039/c2cc31748f>
• Miyake Yoshihiro, Ashida Yuya, Nakajima Kazunari, Nishibayashi Yoshiaki: Visible-light-mediated addition of α-aminoalkyl radicals generated from α-silylamines to α,β-unsaturated carbonyl compounds. Chem. Commun. 2012, 48, 6966. <https://doi.org/10.1039/c2cc32745g>
• Chen Min, Huang Zhi-Tang, Zheng Qi-Yu: Visible light-induced 3-sulfenylation of N-methylindoles with arylsulfonyl chlorides. Chem. Commun. 2012, 48, 11686. <https://doi.org/10.1039/c2cc36866h>
• Zhu Shaoqun, Rueping Magnus: Merging visible-light photoredox and Lewis acid catalysis for the functionalization and arylation of glycine derivatives and peptides. Chem. Commun. 2012, 48, 11960. <https://doi.org/10.1039/c2cc36995h>
• Shi Lei, Xia Wujiong: Photoredox functionalization of C–H bonds adjacent to a nitrogen atom. Chem. Soc. Rev. 2012, 41, 7687. <https://doi.org/10.1039/c2cs35203f>
• Mitkina Tatiana, Stanglmair Christoph, Setzer Wolfgang, Gruber Michael, Kisch Horst, König Burkhard: Visible light mediated homo- and heterocoupling of benzyl alcohols and benzyl amines on polycrystalline cadmium sulfide. Biomol Chem 2012, 10, 3556. <https://doi.org/10.1039/c2ob07053g>
• Hoffmann Norbert: Photochemical reactions of aromatic compounds and the concept of the photon as a traceless reagent. Photochem Photobiol Sci 2012, 11, 1613. <https://doi.org/10.1039/c2pp25074h>
• Xuan Jun, Feng Zhu-Jia, Duan Shu-Wen, Xiao Wen-Jing: Room temperature synthesis of isoquino[2,1-a][3,1]oxazine and isoquino[2,1-a]pyrimidine derivatives via visible light photoredox catalysis. RSC Adv 2012, 2, 4065. <https://doi.org/10.1039/c2ra20403g>
• Ischay Michael A., Ament Michael S., Yoon Tehshik P.: Crossed intermolecular [2 + 2] cycloaddition of styrenes by visible light photocatalysis. Chem. Sci. 2012, 3, 2807. <https://doi.org/10.1039/c2sc20658g>
• Koike Takashi, Yasu Yusuke, Akita Munetaka: Visible-light-driven Oxidation of 1,3-Dicarbonyl Compounds via Catalytic Disproportionation of TEMPO by Photoredox Catalysis. Chemistry Letters 2012, 41, 999. <https://doi.org/10.1246/cl.2012.999>
• Gaikwad A. G.: Transport of Carbonate Ions by Novel Cellulose Fiber Supported Solid Membrane. Bull. Chem. React. Eng. Catal. 2012, 7, 49. <https://doi.org/10.9767/bcrec.7.1.1225.49-57>
• Tucker Joseph W., Stephenson Corey R. J.: Tandem Visible Light-Mediated Radical Cyclization–Divinylcyclopropane Rearrangement to Tricyclic Pyrrolidinones. Org. Lett. 2011, 13, 5468. <https://doi.org/10.1021/ol202178t>
• Rueping Magnus, Zhu Shaoqun, Koenigs René M.: Visible-light photoredox catalyzed oxidative Strecker reaction. Chem Commn 2011, 47, 12709. <https://doi.org/10.1039/c1cc15643h>