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Collect. Czech. Chem. Commun. 1984, 49, 1990-2000
https://doi.org/10.1135/cccc19841990

1,3-Dipolar cycloadditions to 2,3-dimethoxycarbonyl-7-oxabicyclo[2,2,1]-2,5-heptadiene, 1,4-epoxy-1,4-dihydronaphthalene, and exo-endo-1,6-dimethoxycarbonyl-11,12-dioxatetracyclo-[4,4,0,12,5,17,10]-3,8-dodecadiene

Lubor Fišera and Dušan Pavlovič

Department of Organic Chemistry, Slovak Institute of Technology, 812 37 Bratislava

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  • Levandowski Brian J., Graham Brian J., Houk K. N., Raines Ronald T.: Click Organocatalysis: Acceleration of Azide–Alkyne Cycloadditions with Mutually Orthogonal Click Reactions. J. Org. Chem. 2024, 89, 2232. <https://doi.org/10.1021/acs.joc.3c02182>
  • Kaur Jasleen, Saxena Mokshika, Rishi Narayan: An Overview of Recent Advances in Biomedical Applications of Click Chemistry. Bioconjugate Chem. 2021, 32, 1455. <https://doi.org/10.1021/acs.bioconjchem.1c00247>
  • Butler Christopher R., Bendesky Justin, Schoffstall Allen Milton: Regioselective Reduction of 1H-1,2,3-Triazole Diesters. Molecules 2021, 26, 5589. <https://doi.org/10.3390/molecules26185589>
  • Ersoy Elif Basak, Gunkara Omer Tahir, Ocal Nuket: Synthesis of new polyhedral oligomeric silsesquioxane derivatives as some possible antimicrobial agents. Phosphorus, Sulfur, and Silicon and the Related Elements 2019, 194, 257. <https://doi.org/10.1080/10426507.2018.1539721>
  • Chen Wenkun, Yang Wen, Wu Ruihua, Yang Dingqiao: Water-promoted synthesis of fused bicyclic triazolines and naphthols from oxa(aza)bicyclic alkenes and transformation via a novel ring-opening/rearrangement reaction. Green Chem. 2018, 20, 2512. <https://doi.org/10.1039/C7GC03772D>
  • Zaytsev Vladimir P., Mertsalov Dmitriy F., Nadirova Maryana A., Dorovatovskii Pavel V., Khrustalev Victor N., Sorokina Elena A., Zubkov Fedor I., Varlamov Aleksey V.: [3+2] Cycloaddition of o-nitrophenyl azide to 3a,6-epoxyisoindoles. Chem Heterocycl Comp 2017, 53, 1199. <https://doi.org/10.1007/s10593-018-2194-1>
  • Tajabadi J., Bakavoli M., Gholizadeh M., Eshghi H., Izadyar M.: The origin of regio- and stereoselectivity in the 1,3-dipolar cycloaddition of nitrile oxides with C1-substituted 7-oxabenzonorbornadienes, a DFT study. RSC Adv. 2015, 5, 38489. <https://doi.org/10.1039/C5RA04254B>
  • Nagireddy Jaipal R., Carlson Emily, Tam William: 1,3-Dipolar Cycloadditions of Nitrile Oxides with 7-Oxa- and 7-Azabenzonorbornadienes. Can. J. Chem. 2014, 140501143658. <https://doi.org/10.1139/cjc-2014-0140>
  • Soret Adrien, Müller Christine, Guillot Régis, Blanco Luis, Deloisy Sandrine: Short and efficient synthesis of 2H-pyrroles from 7-oxanorbornadiene derivatives. Tetrahedron 2011, 67, 698. <https://doi.org/10.1016/j.tet.2010.11.080>
  • Sultan Nisrine, Thomas Coralie, Blanco Luis, Deloisy Sandrine: Preparation of unsymmetrical dialkyl acetylenedicarboxylates and related esters by enzymatic transesterification. Tetrahetron Lett 2011, 52, 3443. <https://doi.org/10.1016/j.tetlet.2011.04.103>
  • Albert Sébastien, Soret Adrien, Blanco Luis, Deloisy Sandrine: Soluble and polymer-supported 2- and 3-benzylated furans for the preparation of α,β-ethylenic carbonyl compounds. Tetrahedron 2007, 63, 2888. <https://doi.org/10.1016/j.tet.2007.01.030>
  • FISERA L., PAVLOVIC D.: ChemInform Abstract: 1,3‐DIPOLAR CYCLOADDITION OF HETEROCYCLES. XII. 1,3‐DIPOLAR CYCLOADDITIONS TO 2,3‐BIS(METHOXYCARBONYL)‐7‐OXABICYCLO(2.2.1)‐2,5‐HEPTADIENE, 1,4‐EPOXY‐1,4‐DIHYDRONAPHTHALENE, AND EXO,ENDO‐1,6‐BIS(METHOXYCARBONYL)‐11,12‐DIOXATETRACYCLO(4.4.0.12,5.17,10)‐3,8‐DODECADIENE. Chemischer Informationsdienst 1985, 16. <https://doi.org/10.1002/chin.198502091>