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.

引用

页码：1350 / 1356

页数：7

共 44 条

[41] A polymer-supported Cinchona-based bifunctional sulfonamide catalyst: a highly enantioselective, recyclable heterogeneous organocatalyst
Youk, Sung Hun
Oh, Sang Ho
Rho, Ho Sik
Lee, Je Eun
Lee, Ji Woong
Song, Choong Eui
[J]. CHEMICAL COMMUNICATIONS, 2009, (16) : 2220 - 2222
[42] Asymmetric Michael addition reactions of aldehydes with nitrostyrenes catalyzed by functionalized chiral ionic liquids
Zhang, Qianying
Ni, Bukuo
Headley, Allan D.
[J]. TETRAHEDRON, 2008, 64 (22) : 5091 - 5097
[43] Highly enantioselective aldol reactions catalyzed by a recyclable fluorous (S) pyrrolidine sulfonamide on water
Zu, Liansuo
Xie, Hexin
Li, Hao
Wang, Jian
Wang, Wei
[J]. ORGANIC LETTERS, 2008, 10 (06) : 1211 - 1214
[44] A recyclable fluorous (S)-pyrrolidine sulfonamide promoted direct, highly enantioselective Michael addition of ketones and aldehydes to nitroolefins in water
Zu, Liansuo
Wang, Jian
Li, Hao
Wang, Wei
[J]. ORGANIC LETTERS, 2006, 8 (14) : 3077 - 3079

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