Enantioselective Michael additions to α,β-unsaturated imides catalyzed by a Salen-Al complex

被引:255
作者
Taylor, MS [1 ]
Jacobsen, EN [1 ]
机构
[1] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
关键词
D O I
10.1021/ja037177o
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
(Salen)aluminum complex 1b is an efficient catalyst for the conjugate addition of di- and trisubstituted nitriles to a wide range of acyclic alkyl- and aryl-substituted α,β-unsaturated imides. This new methodology provides access to multifunctional compounds that previously have not been readily accessible in enantioenriched form. Synthetic applications of these products include the preparation of enantiomerically enriched piperidines, as exemplified by an expedient asymmetric catalytic synthesis of (-)-paroxetine. Copyright © 2003 American Chemical Society.
引用
收藏
页码:11204 / 11205
页数:2
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