Аннотация:
Deprotonation of 1-alkyl-5-phenyl-1,2,4-triazinium salts by triethylamine results in the formation of azomethyne ylides which undergo a 1,3-dipolar cycloaddition reaction with diethyl acetylenedicarboxylate to yield pyrrolo[2,1-f]1,2,4-triazines
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
O. N. Chupakhin, B. V. Rudakov, S. G. Alexeev, S. V. Shorshnev, V. N. Charushin, “1-Alkyl-1,2,4-triazinium Ylides as 1,3-Dipoles in a Cycloaddition Reaction with Diethyl Acetylenedicarboxylate”, Mendeleev Commun., 2:3 (1992), 85–86
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5415
https://www.mathnet.ru/rus/mendc/v2/i3/p85
Эта публикация цитируется в следующих 11 статьяx:
Veronika Šlachtová, Simona Bellová, Agustina La‐Venia, Juraj Galeta, Martin Dračínský, Karel Chalupský, Alexandra Dvořáková, Helena Mertlíková‐Kaiserová, Peter Rukovanský, Rastislav Dzijak, Milan Vrabel, “Triazinium Ligation: Bioorthogonal Reaction of N1‐Alkyl 1,2,4‐Triazinium Salts**”, Angewandte Chemie, 135:36 (2023)
Veronika Šlachtová, Simona Bellová, Agustina La‐Venia, Juraj Galeta, Martin Dračínský, Karel Chalupský, Alexandra Dvořáková, Helena Mertlíková‐Kaiserová, Peter Rukovanský, Rastislav Dzijak, Milan Vrabel, “Triazinium Ligation: Bioorthogonal Reaction of N1‐Alkyl 1,2,4‐Triazinium Salts**”, Angew Chem Int Ed, 62:36 (2023)
Nataliya N. Mochulskaya, Svetlana K. Kotovskaya, Ilya I. Butorin, Mikhail V. Varaksin, Valery N. Charushin, Vladimir L. Rusinov, Yana L. Esaulkova, Alexander V. Slita, Polina A. Ilyina, Vladimir V. Zarubaev, “Bioactive Pyrrolo[2,1-f][1,2,4]triazines: Synthesis, Molecular Docking, In Vitro Cytotoxicity Assay and Antiviral Studies”, Chemistry, 5:4 (2023), 2657
Juraj Galeta, Veronika Šlachtová, Martin Dračínský, Milan Vrabel, “Regio- and Diastereoselective 1,3-Dipolar Cycloadditions of 1,2,4-Triazin-1-ium Ylides: a Straightforward Synthetic Route to Polysubstituted Pyrrolo[2,1-f][1,2,4]triazines”, ACS Omega, 7:24 (2022), 21233
Gregory R. Ott, David A. Favor, “Pyrrolo[2,1-f][1,2,4]triazines: From C-nucleosides to kinases and back again, the remarkable journey of a versatile nitrogen heterocycle”, Bioorganic & Medicinal Chemistry Letters, 27:18 (2017), 4238
Tho Thieu, Joseph A. Sclafani, Daniel V. Levy, Andrew McLean, Henry J. Breslin, Gregory R. Ott, Roger P. Bakale, Bruce D. Dorsey, “Discovery and Process Synthesis of Novel 2,7-Pyrrolo[2,1-f][1,2,4]triazines”, Org. Lett., 13:16 (2011), 4204
N. N. Mochulskaya, A. A. Andreiko, V. N. Charushin, B. V. Shulgin, D. V. Raikov, V. I. Solomonov, “Intermolecular and intramolecular cycloaddition reactions of 1-ethyl-1,2,4-triazinium salts with alkynes”, Mendeleev Commun., 11:1 (2001), 19–21
Comprehensive Heterocyclic Chemistry II, 1996, 1169
Drago R. Sliskovic, Comprehensive Heterocyclic Chemistry II, 1996, 389
O. N. CHUPAKHIN, B. V. RUDAKOV, S. G. ALEXEEV, S. V. SHORSHNEV, V. N. CHARUSHIN, “ChemInform Abstract: 1‐Alkyl‐1,2,4‐triazinium Ylides as 1,3‐Dipoles in a Cycloaddition Reaction with Diethyl Acetylenedicarboxylate.”, ChemInform, 24:15 (1993)
DEREK T. Hurst, Progress in Heterocyclic Chemistry, 5, A Critical Review of the 1992 Literature Preceded by two Chapters on Current Heterocyclic Topics, 1993, 239
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