化学
马来酰亚胺
铑
烷基
芳基
催化作用
基质(水族馆)
选择性
功能群
反应条件
药物化学
组合化学
有机化学
海洋学
地质学
聚合物
作者
XXXXXXX Manisha,Devesh Chandra,Upendra Sharma
标识
DOI:10.1002/ejoc.202300411
摘要
Abstract An efficient Rh(III)‐catalyzed C−H alkenylation of N ‐protected isoquinolone with maleimides is reported. The carbonyl group of isoquinolone acts as an inherent directing group. Various N ‐substituents in the maleimide, including alkyl, aryl, and even H and −OH, were well tolerated under the developed reaction condition. This protocol showed broad substrate scope, good selectivity, and excellent yields. Hammett plot is also drawn to check the effect of substituents on the reaction progress.
科研通智能强力驱动
Strongly Powered by AbleSci AI