Recent Progress of Sulfonamide Organocatalysts in Asymmetric Catalysis

被引：0
|
作者：
Ban, Shurong [1 ]
Xie, Hongyu [1 ]
Li, Qingshan [1 ]
Zheng, Feilang [1 ]
机构：
[1] Shanxi Med Univ, Sch Pharmaceut Sci, Taiyuan 030001, Peoples R China
来源：
CHINESE JOURNAL OF ORGANIC CHEMISTRY | 2011年 / 31卷 / 09期
关键词：
organocatalysis; sulfonamide; enantioselectivity; recent progress; CHIRAL AMINO SULFONAMIDE; ENANTIOSELECTIVE MICHAEL ADDITION; PYRROLIDINE-SULFONAMIDE; MANNICH REACTIONS; ALDOL REACTIONS; EFFICIENT ORGANOCATALYST; CONJUGATE ADDITION; ALDEHYDES; KETONES; PROLINE;
D O I：
暂无
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Organocatalytic asymmetric reaction is an increasingly active research area in organic synthesis. The recent progresses in sulfonamide-based organocatalytic asymmetric reaction (Michael addition reaction, Mannich reaction, Aldol reaction etc.) are reviewed. The influences of acidity and hydrogen bond-donating properties of NH in sulfonamides on asymmetric reaction are discussed.
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页码：1350 / 1356
页数：7
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