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铑催化不对称1,4-共轭加成反应的研究进展
引用本文:王欢,杨定乔,莫海洪. 铑催化不对称1,4-共轭加成反应的研究进展[J]. 有机化学, 2007, 27(7): 806-818
作者姓名:王欢  杨定乔  莫海洪
作者单位:华南师范大学化学与环境学院,广州,510006
基金项目:广东省自然科学基金(No.04010404)资助项目.
摘    要:铑催化不对称1,4-共轭加成反应是一种非常有效的碳-碳键形成方法. 本文综述了近年来铑催化不对称1,4-共轭加成反应的研究进展, 包括α,β-不饱和酮、酯、酰胺、醛和砜等与某些亲核试剂的1,4-共轭加成反应.

关 键 词:铑催化  不对称  亲核试剂  1,4-共轭加成
收稿时间:2006-07-26
修稿时间:2006-07-262006-10-18

Progress in Rhodium-Catalyzed Asymmetric 1,4-ConjugateAddition Reactions
WANG Huan,YANG Ding-Qiao,MO Hai-Hong. Progress in Rhodium-Catalyzed Asymmetric 1,4-ConjugateAddition Reactions[J]. Chinese Journal of Organic Chemistry, 2007, 27(7): 806-818
Authors:WANG Huan  YANG Ding-Qiao  MO Hai-Hong
Affiliation:School of Chemistry and Environment, South China Normal University, Guangzhou 510006
Abstract:Rhodium-catalyzed asymmetric 1,4-conjugate addition reaction is one of the most efficient methods for the carbon-carbon bond formation. In this paper, the recent progress in rhodium-catalyzed asymmetric 1,4-conjugate addition reactions is reviewed. Asymmetric 1,4-conjugate additions of α,β-unsaturated ketones, esters, amides, aldehydes, sulfones and so on with some nu-cleophiles are presented.
Keywords:rhodium-catalyzed   asymmetric   nucleophile   1,4-conjugate addition
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