化学
立体选择性
催化作用
铜
配体(生物化学)
溶剂
组合化学
有机化学
药物化学
受体
生物化学
作者
Sai‐Hu Cai,Bing‐Chao Da,Jiahui Zhou,Yun‐He Xu,Teck‐Peng Loh
标识
DOI:10.1002/cjoc.201600380
摘要
Abstract An efficient methodology for the stereoselective synthesis of cis ‐2,5‐disubstituted pyrrolidines using copper catalyst was developed. The corresponding cis ‐2,5‐disubstituted pyrrolidines could be obtained in reasonable yields and with good stereoselectivities in the presence of 4,4′‐di‐ tert ‐butyl‐2,2′‐bipyridine as ligand and 1‐methyl‐2‐pyrrolidinone as solvent.
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