STEREOCHEMICAL CONTROL IN MICROBIAL REDUCTION .15. PREPARATION OF (2R,3S)-2-ALLYL-3-HYDROXYBUTANOATE

被引：8

作者：

NAKAMURA, K

MIYAI, T

FUKUSHIMA, K

KAWAI, Y

BABU, BR

OHNO, A

机构：

来源：

BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN | 1990年 / 63卷 / 06期

关键词：

D O I：

10.1246/bcsj.63.1713

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

收藏

页码：1713 / 1715

页数：3

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[6] ENZYMES IN ORGANIC-SYNTHESIS .32. STEREOSPECIFIC HORSE LIVER ALCOHOL DEHYDROGENASE-CATALYZED OXIDATIONS OF EXO-OXABICYCLIN AND ENDO-OXABICYCLIC MESO DIOLS
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[7] STEREOCHEMICAL CONTROL IN MICROBIAL REDUCTION .14. STEREOSELECTIVE SYNTHESIS OF (2R,3S)-SYN-2-ALLYL-3-HYDROXY BUTANOATE MEDIATED BY AN ENZYMATIC SYSTEM FROM BAKERS-YEAST
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[8] STEREOCHEMICAL CONTROL IN MICROBIAL REDUCTION .8. STEREOCHEMICAL CONTROL IN MICROBIAL REDUCTION OF BETA-KETO-ESTERS
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[9] STEREOCHEMICAL CONTROL IN MICROBIAL REDUCTION .9. DIASTEREOSELECTIVE REDUCTION OF 2-ALKYL-3-OXOBUTANOATE WITH BAKERS-YEAST
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[10] A NEW METHOD FOR STEREOCHEMICAL CONTROL OF MICROBIAL REDUCTION - REDUCTION OF BETA-KETO-ESTERS WITH BAKERS-YEAST IMMOBILIZED BY MAGNESIUM ALGINATE
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