DBU-Catalyzed Alkyne-Imidate Cyclization toward 1-Alkoxypyrazino[1,2- a]indole Synthesis

1-(Propargyl)indol-2-carbonitriles react with alcohols to afford 1-alkoxypyrazino[1,2-a]indoles under DBU-catalyzed microwave-assisted conditions. The reaction scope includes a wide range of indoles, primary and secondary alcohols, and a thiol. The initial mechanistic study shows that the domino process presumably proceeds through an alkyne-allene rearrangement, imidate formation, and nucleophilic cyclization reaction sequence. © Copyright 2018 American Chemical Society.

Авторы
Festa A.A. 1 , Zalte R.R. 1 , Golantsov N.E. 1 , Varlamov A.V. 1 , Van Der Eycken E.V. , Voskressensky L.G. 1
Номер выпуска
16
Язык
Английский
Страницы
9305-9311
Статус
Опубликовано
Том
83
Год
2018
Организации
  • 1 Peoples' Friendship University of Russia, RUDN University, Miklukho-Maklaya Street 6, Moscow, 117198, Russian Federation
  • 2 Laboratory for Organic and Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven), Celestijnenlaan 200F, Leuven, B-3001, Belgium
Ключевые слова
Catalysis; Hydrocarbons; Carbonitriles; Cyclization reactions; Domino process; Mechanistic studies; Microwave assisted; Propargyl; Secondary alcohols; Cyclization
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/6453/
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