化学
对映选择合成
废止
催化作用
镍
双环分子
配体(生物化学)
组合化学
有机化学
受体
生物化学
作者
Di Shen,Wu‐Bin Zhang,Zhiyang Li,Shi‐Liang Shi,Youjun Xu
标识
DOI:10.1002/adsc.201901582
摘要
Abstract Reported is a highly enantioselective Ni(0)‐catalyzed endo ‐selective C−H annulation of 2‐ and 4‐pyridone, and 4‐pyrimidone with alkenes to provide drug‐relevant bicyclic heterocycle products. The use of a readily prepared chiral bulky NHC ligand (SIPE) for Ni catalyst and commercially available AlEt 3 as co‐catalyst enhanced the practicality of this reaction. magnified image
科研通智能强力驱动
Strongly Powered by AbleSci AI