化学
酰化
亲核细胞
位阻效应
吡啶
药物化学
有机化学
组合化学
催化作用
作者
Atsushi Umehara,Soma Shimizu,Makoto Sasaki
标识
DOI:10.1002/adsc.202300487
摘要
Abstract This report describes a general method for the one‐pot direct N ‐acylation of N ‐heterocycles using our previously developed 4‐( N , N ‐dimethylamino)pyridine N ‐oxide (DMAPO)/di‐ tert ‐butyl dicarbonate (Boc 2 O) system. This system enables one‐pot N ‐acylation reactions to provide bulky N ‐acyl heterocycles starting from a wide variety of less nucleophilic N ‐heterocycles and sterically hindered α‐fully substituted carboxylic acids in high yields. Moreover, this one‐pot method does not involve pre‐activation of substrates. The protocol has been successfully extended to one‐pot N ‐acylation of 7‐azaindoles.
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