Ruthenium-catalysed one-pot regio- and diastereoselective synthesis of pyrrolo[1,2-a] indoles via cascade C-H functionalization/annulation

A cascade approach has been developed towards dual C-C bond formation via consecutive C-H functionalization/cyclization giving access to pyrrolo[1,2-a]indoles in a highly regio- and diastereoselective manner using catalytic [Ru(p-cymene)Cl2]2. The methodology was further expanded to attain pentacyclic structures involving manifold C-C bond creation. © 2017 The Royal Society of Chemistry.

Авторы
Singh S.1 , Butani H.H.1, 2 , Vachhani D.D.2 , Shah A.2 , Van Der Eycken E.V.
Издательство
Royal Society of Chemistry
Номер выпуска
78
Язык
Английский
Страницы
10812-10815
Статус
Опубликовано
Том
53
Год
2017
Организации
  • 1 Laboratory for Organic and Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven, KU Leuven, Celestijnenlaan 200F, Leuven, B-3001, Belgium
  • 2 Department of Chemistry, Saurashtra University, Rajkot, India
  • 3 Peoples Friendship University of Russia, RUDN University, Miklukho-Maklaya street 6, Moscow, 117198, Russian Federation
Ключевые слова
carbon; hydrogen; indole derivative; pyrrolo[1,2 a]indole derivative; ruthenium; unclassified drug; annulation reaction; Article; catalysis; chemical reaction; diastereoisomer; functionalization reaction; hydrogen bond; Michael addition; one pot synthesis; regioselectivity; stereoselectivity
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/6180/
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