Transition-Metal-Free Base-Controlled C−N Coupling Reactions: Selective Mono Versus Diarylation of Primary Amines with 2-Chlorobenzimidazoles; Advanced Synthesis and Catalysis; Vol. 363, iss. 5

Transition-Metal-Free Base-Controlled C−N Coupling Reactions: Selective Mono Versus Diarylation of Primary Amines with 2-Chlorobenzimidazoles; Advanced Synthesis and Catalysis; Vol. 363, iss. 5

Библиографические подробности
Источник:	Advanced Synthesis and Catalysis Vol. 363, iss. 5.— 2021.— [P. 1408-1416]
Автор-организация:	Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
Другие авторы:	Wei Sang, Yan-Yan Gong, Hua Cheng, Rui Zhang, Ye Yuan, Guang-Gao Fan, Zhi-Qin Wang, Cheng Chen, Verpoort F. V. K. Frensis Valter Kornelius
Примечания:	Title screen Herein, a base-controlled protocol was developed for the C−N coupling of primary amines and 2-chlorobenzimidazoles, affording a handful of secondary or tertiary amines in a selective fashion. Moreover, this protocol was realized under transition-metal-free conditions, and the variation of the base from iPr2NH to LiOtBu completely switched the selectivity from monoarylation to diarylation. Further investigations elucidated that the variety, intrinsic basicity and amount of the utilized bases considerably affected these reactions.
Язык:	английский
Опубликовано:	2021
Предметы:	электронный ресурс труды учёных ТПУ transition-metal-free base-controlled CN coupling diarylation monoarylation 2-aminobenzimida-zoles переходные металлы амины
Online-ссылка:	https://doi.org/10.1002/adsc.202001365
Формат:	Электронный ресурс Статья
Запись в KOHA:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=667545

Internet

https://doi.org/10.1002/adsc.202001365