对映选择合成
化学
磺胺
催化作用
二胺
炔基化
芳基
有机化学
组合化学
药物化学
烷基
作者
Hongmin Qu,Yu Chen,Xiangling Ceng,Pei Tang,Huijing Wang,Fen‐Er Chen
标识
DOI:10.1002/ajoc.202200188
摘要
Abstract The catalytic enantioselective alkynylation of isatins, catalyzed by a Zn(OCOCF 3 ) 2 /chiral bis(sulfonamide)‐diamine (BSDA) catalyst under mild condition, has been developed. The desired chiral 3‐alkynyl‐3‐hydroxy‐2‐oxindoles were obtained in moderate to excellent yields (up to 96%) and good to excellent enantioselectivites (up to 97% ee ). The reaction is broad in scope with respect to aryl‐substituted terminal alkynes and substituted isatins.
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