环丙烷
环加成
化学
路易斯酸
催化作用
对映选择合成
接受者
手性路易斯酸
立体化学
有机化学
组合化学
戒指(化学)
药物化学
物理
凝聚态物理
作者
Ming Bao,Michael P. Doyle
出处
期刊:Chemcatchem
[Wiley]
日期:2023-10-18
卷期号:15 (23)
被引量:7
标识
DOI:10.1002/cctc.202301090
摘要
Abstract [3+ n ]‐Cycloaddition reactions that employ donor‐acceptor cyclopropanes using either chiral catalysts and racemic cyclopropanes or achiral catalysts and chiral, non‐racemic, cyclopropanes have become useful transformations for the construction of carbocyclic and heterocyclic compounds, with both processes offering mechanistic and structural advantages in ring formation. Although the vast majority of asymmetric cycloaddition reactions of donor‐acceptor cyclopropanes have been performed with racemic cyclopropane compounds catalyzed by Lewis acids with chiral ligands, optically active cyclopropane compounds can serve the same role using Lewis acids without chiral ligands. This review covers the use of chiral catalysts with racemic donor‐acceptor cyclopropanes and the use of chiral non‐racemic donor‐acceptor cyclopropanes with achiral Lewis acid catalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI