Asymmetric allylic alkylation, an enabling methodology

被引:482
作者
Trost, BM [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
关键词
D O I
10.1021/jo0491004
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The diversity of mechanisms for enantiodiscrimination and of bond types that can be formed make Pd-catalyzed asymmetric allylic alkylation a powerful key step for simplification of synthetic strategy to complex molecular targets. Using a wide range of different classes of compounds including alkaloids, polyhydrofurans, nucleosides and carbanucleosides, cyclohexitols and cyclopentitols, chromanes, cyclopentanoids, amino acids, barbiturates, etc., novel synthetic strategies emerge that provide short efficient asymmetric syntheses.
引用
收藏
页码:5813 / 5837
页数:25
相关论文
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