Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1996, 61, 1047-1052
https://doi.org/10.1135/cccc19961047

Alkaloids from Papaver setigerum DC.

Jiří Slavík and Leonora Slavíková

Biochemical Institute of Medical Faculty, Masaryk University, 662 43 Brno, Czech Republic

Crossref Cited-by Linking

  • Yadav Neetu, Gopalaiah Kovuru, Pandey Jyoti, Nagarajan Rajamani: Zircon PrVO4: an efficient heterogeneous catalyst for tandem oxidative synthesis of 2,3-disubstituted quinoline derivatives. Dalton Trans. 2023, 52, 5969. <https://doi.org/10.1039/D3DT00435J>
  • Tittarelli Roberta, Gismondi Angelo, Di Marco Gabriele, Mineo Federico, Vernich Francesca, Russo Carmelo, Marsella Luigi Tonino, Canini Antonella: Forensic Application of Genetic and Toxicological Analyses for the Identification and Characterization of the Opium Poppy (Papaver somniferum L.). Biology 2022, 11, 672. <https://doi.org/10.3390/biology11050672>
  • Shen Xiao-Qin, Yan Xiao-Wei, Zhang Xing-Guo: A palladium-catalyzed ring-expansion reaction of cyclobutanols with 2-haloanilines leading to benzazepines and quinolines. Chem. Commun. 2021, 57, 10234. <https://doi.org/10.1039/D1CC04395A>
  • Lang Dean E., Morris Jeremy S., Rowley Michael, Torres Miguel A., Maksimovich Vook A., Facchini Peter J., Ng Kenneth K.S.: Structure–function studies of tetrahydroprotoberberine N-methyltransferase reveal the molecular basis of stereoselective substrate recognition. Journal of Biological Chemistry 2019, 294, 14482. <https://doi.org/10.1074/jbc.RA119.009214>
  • Sharma Shweta, Kumar Mukesh, Vishwakarma Ram A., Verma Mahendra K., Singh Parvinder Pal: Room Temperature Metal-Catalyzed Oxidative Acylation of Electron-Deficient Heteroarenes with Alkynes, Its Mechanism, and Application Studies. J. Org. Chem. 2018, 83, 12420. <https://doi.org/10.1021/acs.joc.8b01475>
  • He Yimiao, Wang Xuelian, Xiao Jun-An, Pang Jinying, Gan Chunfang, Huang Yanmin, Huang Chusheng: Metal-free oxidative isocyanides insertion with aromatic aldehydes to aroylated N-heterocycles. RSC Adv. 2018, 8, 3036. <https://doi.org/10.1039/C7RA12755C>
  • Siddaraju Yogesh, Prabhu Kandikere Ramaiah: Transition metal-free Minisci reaction promoted by NCS, and TBHP: acylation of heteroarenes. Tetrahedron 2016, 72, 959. <https://doi.org/10.1016/j.tet.2015.12.065>
  • Ali Wajid, Behera Ahalya, Guin Srimanta, Patel Bhisma K.: Regiospecific Benzoylation of Electron-Deficient N-Heterocycles with Methylbenzenes via a Minisci-Type Reaction. J. Org. Chem. 2015, 80, 5625. <https://doi.org/10.1021/acs.joc.5b00501>
  • Modi Anju, Ali Wajid, Mohanta Prakash R., Khatun Nilufa, Patel Bhisma K.: CuO Nanoparticle Catalyzed Synthesis of 2,3-Disubstituted Quinazolinones via Sequential N-Arylation and Oxidative C–H Amidation. ACS Sustainable Chem. Eng. 2015, 3, 2582. <https://doi.org/10.1021/acssuschemeng.5b00817>
  • Melzer Benedikt, Bracher Franz: A divergent approach to benzylisoquinoline-type and oxoaporphine alkaloids via regioselective direct ring metalation of alkoxy isoquinolines. Org. Biomol. Chem. 2015, 13, 7664. <https://doi.org/10.1039/C5OB00926J>
  • Siddaraju Yogesh, Lamani Manjunath, Prabhu Kandikere Ramaiah: A Transition Metal-Free Minisci Reaction: Acylation of Isoquinolines, Quinolines, and Quinoxaline. J. Org. Chem. 2014, 79, 3856. <https://doi.org/10.1021/jo500294z>
  • Matcha Kiran, Antonchick Andrey P.: Metal‐Free Cross‐Dehydrogenative Coupling of Heterocycles with Aldehydes. Angewandte Chemie 2013, 125, 2136. <https://doi.org/10.1002/ange.201208851>
  • Matcha Kiran, Antonchick Andrey P.: Metal‐Free Cross‐Dehydrogenative Coupling of Heterocycles with Aldehydes. Angew Chem Int Ed 2013, 52, 2082. <https://doi.org/10.1002/anie.201208851>
  • Zhu Yan‐Ping, Liu Mei‐Cai, Cai Qun, Jia Feng‐Cheng, Wu An‐Xin: A Cascade Coupling Strategy for One‐Pot Total Synthesis of β‐Carboline and Isoquinoline‐Containing Natural Products and Derivatives. Chemistry A European J 2013, 19, 10132. <https://doi.org/10.1002/chem.201301734>
  • Lee Chul, Choe Sanggil, Lee Jin Woo, Jin Qinghao, Lee Mi Kyeong, Hwang Bang Yeon: Alkaloids from Papaver setigerum. Bulletin of the Korean Chemical Society 2013, 34, 1290. <https://doi.org/10.5012/bkcs.2013.34.4.1290>
  • Choe Sanggil, Lee Eunjung, Jin Gang-nam, Lee Yang Han, Kim Soo Young, Choi Hwakyung, Chung Heesun, Hwang Bang Yeon, Kim Suncheun: Genetic and chemical components analysis of Papaver setigerum naturalized in Korea. Forensic Science International 2012, 222, 387. <https://doi.org/10.1016/j.forsciint.2012.08.002>
  • Choe Sanggil, Kim Suncheun, Lee Chul, Yang Wonkyung, Park Yuran, Choi Hwakyung, Chung Heesun, Lee Dongho, Hwang Bang Yeon: Species identification of Papaver by metabolite profiling. Forensic Science International 2011, 211, 51. <https://doi.org/10.1016/j.forsciint.2011.04.015>
  • Jacobs Jan, van Tuyen Nguyen, Markusse Peter, Stevens Christian V., Maat Leendert, De Kimpe Norbert: New synthesis of 1-[(3,4-dimethoxyphenyl)methoxymethyl]-6,7-dimethoxyisoquinoline (setigerine), a naturally occurring alkaloid, and some derivatives of papaverine. Tetrahedron 2009, 65, 1188. <https://doi.org/10.1016/j.tet.2008.11.077>
  • Yilmaz Ayhan, Uludağ Nesimi, Morgil Fatma Inci: Alkaloide — ein Unterrichtsthema mit historischen, chemischen und präventiven Bezügen. Chemkon 2004, 11, 21. <https://doi.org/10.1002/ckon.200410003>
  • El Sayed Khalid A.: Microbial transformation of papaveraldine. Phytochemistry 2000, 53, 675. <https://doi.org/10.1016/S0031-9422(99)00616-0>
  • Marek Radek, Humpa Otakar, Dostál Jiří, Slavík Jiří, Sklenář Vladimír: 15N NMR study of isoquinoline alkaloids. Magn Reson Chem 1999, 37, 195. <https://doi.org/10.1002/(SICI)1097-458X(199903)37:3<195::AID-MRC435>3.0.CO;2-D>
  • Marek Radek, Humpa Otakar, Dostál Jiří, Slavík Jiří, Sklenář Vladimír: 15N NMR study of isoquinoline alkaloids. Magn. Reson. Chem. 1999, 37, 195. <https://doi.org/10.1002/(SICI)1097-458X(199903)37:3<195::AID-MRC435>3.0.CO;2-D>
  • W. Bentley Kenneth: β-Phenylethylamines and the isoquinoline alkaloids. Nat. Prod. Rep. 1998, 15, 341. <https://doi.org/10.1039/a815341y>
  • SLAVIK J., SLAVIKOVA L.: ChemInform Abstract: Alkaloids of the Papaveraceae. Part 95. Alkaloids from Papaver setigerum DC. ChemInform 1996, 27. <https://doi.org/10.1002/chin.199646247>