Enantioselective Tsuji allylations

被引:310
作者
Mohr, Justin T. [1 ]
Stoltz, Brian M. [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Arnold & Mabel Beckman Labs Chem Synt, Pasadena, CA 91125 USA
关键词
allylation; asymmetric catalysis; enols; ketones; palladium; ASYMMETRIC ALLYLIC ALKYLATION; QUATERNARY CARBON CENTERS; PALLADIUM-CATALYZED ALLYLATION; PI-ALLYLPALLADIUM COMPLEXES; SILYL ENOL ETHERS; TAIWANIA-CRYPTOMERIOIDES; BETA-KETOESTERS; ORGANOPALLADIUM CHEMISTRY; ALPHA-FLUOROKETONES; SYNTHETIC REACTIONS;
D O I
10.1002/asia.200700183
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The family of allylation reactions developed by Tsuji in the 1980s are capable of generating tertiary and quaternary carbon stereocenters from several synthetic precursors. Despite the utility of these transformations, they have seen little use in the synthesis of natural products. Recently, the power of these reactions was significantly enhanced by the development of enantioselective versions of these transformations. Applications of these methods to the enantioselective syntheses of natural products and pharmaceutical compounds highlight the importance of these developments.
引用
收藏
页码:1476 / 1491
页数:16
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