USE OF BIOLOGICAL METHOD FOR THE PREPARATION OF CHIRAL SYNTHONS - I-REDUCTION OF ACYCLIC BETA-DIKETONES BY SACCHAROMYCES-CEREVISAE (BAKERS-YEAST)

被引：34

作者：

BOLTE, J ^{[1
]}

GOURCY, JG ^{[1
]}

VESCHAMBRE, H ^{[1
]}

机构：

[1] UNIV CLERMONT FERRAND 2,CNRS,CHIM ORGAN BIOL LAB,U485,BP 45,F-63170 AUBIERE,FRANCE

来源：

TETRAHEDRON LETTERS | 1986年 / 27卷 / 05期

关键词：

D O I：

10.1016/S0040-4039(00)84041-1

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：565 / 568

页数：4

共 29 条

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[3] ANITA H, 1982, TETRAHEDRON LETT, V23, P4051
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[5] CHIRAL CYCLOHEXANOID SYNTHETIC PRECURSORS VIA ASYMMETRIC MICROBIAL REDUCTION OF PROCHIRAL CYCLOHEXANEDIONES
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[J]. TETRAHEDRON LETTERS, 1984, 25 (12) : 1241 - 1244
[6] ABOUT THE STEREOSPECIFIC ALPHA-ALKYLATION OF BETA-HYDROXYESTERS
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[J]. HELVETICA CHIMICA ACTA, 1979, 62 (08) : 2825 - 2828
[7] STEREOSPECIFIC SYNTHESIS OF (+)-(3R,4R)-4-METHYL-3-HEPTANOL - ENANTIOMER OF A PHEROMONE OF THE SMALLER EUROPEAN ELM BARK BEETLE (SCOLYTUS-MULTISTRIATUS)
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[J]. HELVETICA CHIMICA ACTA, 1979, 62 (08) : 2829 - 2832
[8] ON THE STERIC COURSE OF BAKER YEAST MEDIATED REDUCTION OF ALKYL 4-AZIDO-3-OXOBUTYRATE AND 4-BROMO-3-OXOBUTYRATE - SYNTHESIS OF (R)-CARNITIN AND (S)-CARNITIN
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[J]. TETRAHEDRON LETTERS, 1985, 26 (01) : 101 - 104
[9] ENANTIOSPECIFIC SYNTHESIS OF OPTICALLY PURE (3S)-HYDROXY ESTERS BY THE STEREOCONTROLLED YEAST REDUCTION OF ALPHA-SULFENYL-BETA-KETOESTERS
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[J]. TETRAHEDRON LETTERS, 1984, 25 (44) : 5083 - 5086
[10] SYNTHESIS OF NONACTIC ACID
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[J]. HELVETICA CHIMICA ACTA, 1974, 57 (07) : 2306 - 2321

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