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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 1992, том 2, выпуск 3, страницы 85–86 (Mi mendc5415)

Эта публикация цитируется в 11 статьях

1-Alkyl-1,2,4-triazinium Ylides as 1,3-Dipoles in a Cycloaddition Reaction with Diethyl Acetylenedicarboxylate

O. N. Chupakhina, B. V. Rudakovb, S. G. Alexeevb, S. V. Shorshnevc, V. N. Charushind

a I. Ya. Postovsky Institute of Organic Synthesis, Urals Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
b Urals State Technical University, Ekaterinburg, Russian Federation
c Ural Scientific Research Institute of Technology of Medical Preparations, Ekaterinburg, Russian Federation
d Department of Organic Chemistry, Urals State Technical University, Ekaterinburg, Russian Federation

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.

Язык публикации: английский

DOI: 10.1070/MC1992v002n03ABEH000144



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