Pd- and Mo-Catalyzed Asymmetric Allylic Alkylation

被引:190
|
作者
Trost, Barry M. [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
ENANTIOSELECTIVE TOTAL-SYNTHESIS; CONCISE SYNTHESIS; CONDURITOL B; STRATEGY; TRANSFORMATIONS; LIGANDS; AAA; CHROMANS; CENTERS; ESTERS;
D O I
10.1021/op200294r
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The ability to control the alkylation of organic substrates becomes ever more powerful by using metal catalysts. Among the major benefits of metal catalysis is the possibility to perform such processes asymmetrically using only catalytic amounts of the chiral inducing agent which is a ligand to the metal of the catalyst. A unique aspect of asymmetric metal-catalyzed processes is the fact that many mechanisms exist for stereoinduction. Furthermore, with the use of the same catalyst system, many types of bonds including but not limited to C-C, C-N, C-O, C-S, C-P, and C-H can be formed asymmetrically. An overview of this process using palladium- and molybdenum-based metals being developed in my laboratories and how it influences strategy in synthesizing bioactive molecular targets is presented.
引用
收藏
页码:185 / 194
页数:10
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