Enantioselective addition of diethylzinc to aldehydes using 1,1'-bi-2-naphthol-3,3'-dicarboxamide as a chiral auxiliary

被引：53

作者：

Kitajima, H ^{[1
]}

Ito, K ^{[1
]}

Katsuki, T ^{[1
]}

机构：

[1] KYUSHU UNIV 33, FAC SCI, DEPT CHEM, HIGASHI KU, FUKUOKA 81281, JAPAN

来源：

CHEMISTRY LETTERS | 1996年 / 05期

关键词：

D O I：

10.1246/cl.1996.343

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A highly enantioselective addition of diethylzinc to a wide range of aldehydes was achieved by using N,N,N',N'-tetraalkyl 1,1'-bi-2-naphthol-3,3'-dicarboxamides as chiral auxiliaries.

引用

页码：343 / 344

页数：2

共 13 条

[11] CATALYTIC ASYMMETRIC-SYNTHESIS OF OPTICALLY-ACTIVE ALKYNYL ALCOHOLS
SOAI, K
NIWA, S
[J]. CHEMISTRY LETTERS, 1989, (03) : 481 - 484
[12] POLYMER-BOUND N-ALKYLNOREPHEDRINES AS EFFICIENT CHIRAL CATALYSTS FOR THE ENANTIOSELECTIVE ADDITION OF DIALKYLZINCS TO BOTH AROMATIC AND ALIPHATIC-ALDEHYDES
SOAI, K
NIWA, S
WATANABE, M
[J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1989, (01): : 109 - 113
[13] AN AB-INITIO MOLECULAR-ORBITAL STUDY ON THE AMINO ALCOHOL-PROMOTED REACTION OF DIALKYLZINCS AND ALDEHYDES
YAMAKAWA, M
NOYORI, R
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (23) : 6327 - 6335

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