对映选择合成
硝基苯
氮丙啶
催化作用
铑
组合化学
化学
环戊二烯基络合物
有机化学
戒指(化学)
作者
Juanjuan Wang,Mupeng Luo,Yi‐Jie Gu,Yuying Liu,Qin Yin,Shouguo Wang
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-01-27
卷期号:63 (12): e202400502-e202400502
被引量:26
标识
DOI:10.1002/anie.202400502
摘要
Abstract Chiral cyclopentadienyl‐rhodium(III) Cp x Rh(III) catalysis has been demonstrated to be competent for catalyzing highly enantioselective aziridination of challenging unactivated terminal alkenes and nitrene sources. The chiral Cp x Rh(III) catalysis system exhibited outstanding catalytic performance and wide functional group tolerance, yielding synthetically important and highly valuable chiral aziridines with good to excellent yields and enantioselectivities (up to 99 % yield, 93 % ee). This protocol presents a novel and effective strategy for synthesizing enantioenriched aziridines from simple alkenes. Various transformations were performed on the aziridine products, illustrating the versatility and synthetic potential of this protocol for constructing highly functionalized compounds.
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