对映选择合成
化学
邻接
环氧乙烷
组合化学
催化作用
有机催化
立体化学
药物发现
合理设计
全合成
有机化学
不对称氢化
立体异构
作者
Mingshuai Zhang,MeiHong Luo,Hao Wang
标识
DOI:10.1002/ejoc.202501098
摘要
The strategic incorporation of α‐chiral centers into carbonyl bioisosteres is a powerful approach for improving the physicochemical and pharmacological profiles of drug candidates. This review summarizes recent advances in the catalytic asymmetric synthesis of vicinal chiral carbonyl bioisosteres, focusing on difluoromethylene, gem‐difluoroalkene, and oxetane motifs. We highlight transition‐metal and organocatalyzed methodologies that achieve high stereocontrol and broad functional group tolerance. Representative examples are analyzed to illustrate key mechanistic pathways, stereochemical models, and applications in late‐stage functionalization. While significant progress has been made, we also discuss persistent challenges regarding generality, efficiency, and mechanistic understanding. Finally, we outline future research directions to guide the rational design of catalytic systems and novel molecular scaffolds, thereby accelerating the discovery of high‐performance pharmaceuticals based on chiral bioisosteres.
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