KINETIC RESOLUTION OF RACEMIC ALDEHYDES BY ENANTIOSELECTIVE ALKYLATION

被引：9

作者：

HAYASHI, M ^{[1
]}

MIWATA, H ^{[1
]}

OGUNI, N ^{[1
]}

机构：

[1] YAMAGUCHI UNIV, FAC SCI, DEPT CHEM, YAMAGUCHI 753, JAPAN

来源：

CHEMISTRY LETTERS | 1989年 / 11期

关键词：

D O I：

10.1246/cl.1989.1969

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1969 / 1970

页数：2

共 10 条

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[4] CATALYTIC ASYMMETRIC INDUCTION - HIGHLY ENANTIOSELECTIVE ADDITION OF DIALKYLZINCS TO ALDEHYDES [J].

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[5]

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[6] A PRACTICAL, EFFICIENT METHOD FOR PREPARATION OF 4 POSSIBLE STEREOISOMERS OF SECONDARY ALLYLIC ALCOHOLS USING KINETIC RESOLUTION OF (E)-1-TRIMETHYLSILYLALK-1-EN-3-OL BY THE SHARPLESS PROCESS [J].

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[7] KINETIC RESOLUTION OF RACEMIC ALLYLIC ALCOHOLS BY ENANTIOSELECTIVE EPOXIDATION - A ROUTE TO SUBSTANCES OF ABSOLUTE ENANTIOMERIC PURITY [J].

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[9] ENANTIOSELECTIVE ADDITION OF DIETHYLZINC TO BENZALDEHYDE CATALYZED BY A SMALL AMOUNT OF CHIRAL 2-AMINO-1-ALCOHOLS [J].

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[10] CATALYTIC ASYMMETRIC INDUCTION - HIGHLY ENANTIOSELECTIVE ADDITION OF DIALKYLZINCS TO ALDEHYDES USING CHIRAL PYRROLIDINYLMETHANOLS AND THEIR METAL-SALTS [J].

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