RUS  ENG
Полная версия
ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2020, том 30, выпуск 6, страницы 712–713 (Mi mendc1300)

Эта публикация цитируется в 5 статьях

Rapid metal free construction of 3-positioned 2-pyridyl substituent in indoles

M. I. Savchuka, I. S. Kovaleva, V. L. Rusinovab, D. S. Kopchukab, A. P. Krinochkinab, G. V. Zyryanovab, O. N. Chupakhinab, V. N. Charushinab

a Institute of Chemical Engineering, Ural Federal University, Ekaterinburg, Russian Federation
b I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation

Аннотация: New access to substituted 2-(indol-3-yl)pyridines involves two stage protocol, namely, a reaction of deoxygenative nucleophilic substitution of hydrogen in 1,2,4-triazine-4-oxides under the action of indoles followed by aza-Diels–Alder reaction of thus obtained 5-indolyl-1,2,4-triazines with 2,5-norbornadiene in a pressure vessel. The reactions sequence provides good yields and is suitable for wide scope of substituted 1,2,4-triazines.

Ключевые слова: 2-(indol-3-yl)pyridines, nucleophilic substitution of hydrogen, aza-Diels–Alder reaction, 1,2,4-triazines, pyridines.

Язык публикации: английский

DOI: 10.1016/j.mencom.2020.11.007



© МИАН, 2024