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有机小分子催化的β-酮酯不对称α-官能化反应 被引量:1

Organocatalytic Asymmetric α-Functionalization of β-Ketoesters
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摘要 有机小分子催化的不对称反应是目前有机化学的研究热点之一。β-酮酯是一类具有活泼次甲基的"软"亲核试剂,可以在有机碱或者金属路易斯酸的催化下进行α-官能化反应。本文详细介绍了有机催化的β-酮酯不对称α-官能化反应的最新研究进展,并对不同亲电试剂参与β-酮酯的α-官能化反应进行了简要评述。 Asymmetric organocatalysis has attracted a considerable amount attention for organic chemists. Due to the α-acidic hydrogen, β-ketoesters could be functionalized in the presence of organic base or metal Lewis acid. Recent development of organocatalytic asymmetric α-functionalization of β-ketoesters reactions is reviewed, and various electrophiles of these reactions are described.
出处 《化学进展》 SCIE CAS CSCD 北大核心 2010年第9期1679-1686,共8页 Progress in Chemistry
关键词 不对称合成 有机催化 β-酮酯 α-官能化反应 asymmetric synthesis organocatalysis β-ketoesters α-functionalization
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