Evaluation of the relationship between the catalyst structure and regio- as well as stereoselectivity in the chiral ammonium bifluoride-catalyzed asymmetric addition of silyl nitronates to α,β-unsaturated aldehydes

被引：9

作者：

Ooi, T ^{[1
]}

Morimoto, K ^{[1
]}

Doda, K ^{[1
]}

Maruoka, K ^{[1
]}

机构：

[1] Kyoto Univ, Grad Sch Sci, Dept Chem, Sakyo Ku, Kyoto 6068502, Japan

来源：

CHEMISTRY LETTERS | 2004年 / 33卷 / 07期

关键词：

D O I：

10.1246/cl.2004.824

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Unique relationship between the catalyst structure and regio- and stereo selectivity in the chiral quaternary ammonium bifluoride-catalyzed asymmetric addition of silyl nitronates to alpha,beta-unsaturated aldehydes has been reported.

引用

页码：824 / 825

页数：2

相关论文

共 3 条

[1] Highly enantioselective Michael addition of silyl nitronates to α,β-unsaturated aldehydes catalyzed by designer chiral ammonium bifluorides: Efficient access to optically active γ-nitro aldehydes and their enol silyl ethers
1600, American Chemical Society (125):
[2] Highly enantioselective Michael addition of silyl nitronates to α,β-unsaturated aldehydes catalyzed by designer chiral ammonium bifluorides:: Efficient access to optically active γ-nitro aldehydes and their enol silyl ethers
Ooi, T
Doda, K
Maruoka, K
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (30) : 9022 - 9023
[3] Asymmetric Michael addition of silyl nitronates to cyclic α,β-unsaturated ketones catalyzed by chiral quaternary ammonium bifluorides:: isolation and selective functionalization of enol silyl ethers of optically active γ-nitro ketones
Ooi, T
Doda, K
Takada, S
Maruoka, K
TETRAHEDRON LETTERS, 2006, 47 (02) : 145 - 148

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