化学
废止
钯
羰基化
催化作用
亲核取代
亲核细胞
组合化学
药物化学
有机化学
一氧化碳
作者
Yang Yuan,Xiao‐Feng Wu
标识
DOI:10.1002/ejoc.201900232
摘要
A simple and efficient synthesis of pyrido‐fused quinazolinones and dibenzoxazepinones by palladium‐catalyzed annulation of commercially available substituted 1‐chloro‐2‐fluorobenzenes and 2‐aminopyridines or 2‐aminophenols has been developed. The reaction involves carbonylation/aromatic nucleophilic substitution sequential in a one‐pot manner.
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