ASYMMETRIC ALDOL-TYPE REACTION BETWEEN BOTH ACHIRAL KETENE SILYL ACETALS AND ALDEHYDES BY THE USE OF A CHIRAL PROMOTER

被引：38

作者：

KOBAYASHI, S

SANO, T

MUKAIYAMA, T

机构：

来源：

CHEMISTRY LETTERS | 1989年 / 08期

关键词：

D O I：

10.1246/cl.1989.1319

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1319 / 1322

页数：4

共 13 条

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[7] ASYMMETRIC ALDOL REACTION OF SILYL ENOL ETHERS WITH ALDEHYDES PROMOTED BY THE COMBINED USE OF CHIRAL DIAMINE COORDINATED TIN(II) TRIFLATE AND TRIBUTYLTIN FLUORIDE [J].

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[8] PERFECT STEREOCHEMICAL CONTROL IN THE SYNTHESIS OF SYN-ALPHA-METHYL-BETA-HYDROXY THIOESTERS BY ASYMMETRIC ALDOL REACTION OF SILYL ENOL ETHERS WITH ALDEHYDES [J].

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[9] IMPROVED ENANTIOSELECTIVE SYNTHESIS OF ANTI ALPHA-METHYL-BETA-HYDROXYESTERS THROUGH TICL4-PPH3 MEDIATED ALDOL CONDENSATION [J].

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