SUBSTRATE MODIFICATION AS A MEANS OF ENHANCING THE ENANTIOSELECTIVITY OF MICROBIAL REDUCTIONS OF BETA-KETO-ESTERS - AN (R)-1,3,5-TRIHYDROXYPENTANE OR (S)-1,3,5-TRIHYDROXYPENTANE SYNTHON

被引：34

作者：

BROOKS, DW ^{[1
]}

KELLOGG, RP ^{[1
]}

COOPER, CS ^{[1
]}

机构：

[1] PURDUE UNIV,DEPT CHEM,W LAFAYETTE,IN 47907

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1987年 / 52卷 / 02期

关键词：

D O I：

10.1021/jo00378a007

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：192 / 196

页数：5

共 25 条

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[2] PROOF THAT THE ABSOLUTE-CONFIGURATION OF NATURAL ALPHA-LIPOIC ACID IS R BY THE SYNTHESIS OF ITS ENANTIOMER [(S)-(-)-ALPHA-LIPOIC ACID] FROM (S)-MALIC ACID
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[3] REMOTE SUBSTITUENT EFFECTS IN MICROBIAL REDUCTIONS OF 3-KETOGLUTARATE AND 3-KETOADIPATE ESTERS
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[4] CHIRAL CYCLOHEXANOID SYNTHETIC PRECURSORS VIA ASYMMETRIC MICROBIAL REDUCTION OF PROCHIRAL CYCLOHEXANEDIONES
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[J]. TETRAHEDRON LETTERS, 1984, 25 (12) : 1241 - 1244
[5] REQUIREMENTS FOR STEREOSPECIFICITY IN HYDROLYSIS BY ALPHA-CHYMOTRYPSIN .4. HYDROXYL SUBSTITUENT - ABSOLUTE CONFIGURATIONS
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[6] ALPHA-METHOXY-ALPHA-TRIFLUOROMETHYLPHENYLACETIC ACID, A VERSATILE REAGENT FOR DETERMINATION OF ENANTIOMERIC COMPOSITION OF ALCOHOLS AND AMINES
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[J]. JOURNAL OF ORGANIC CHEMISTRY, 1969, 34 (09) : 2543 - &
[7] ASYMMETRIC REDUCTION OF CARBONYL-COMPOUNDS BY YEAST .2. PREPARATION OF OPTICALLY-ACTIVE ALPHA-HYDROXY AND BETA-HYDROXY CARBOXYLIC-ACID DERIVATIVES
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[J]. AUSTRALIAN JOURNAL OF CHEMISTRY, 1976, 29 (11) : 2459 - 2467
[8] GUZIEC FS, 1980, SYNTHESIS-STUTTGART, P691
[9] ENANTIOSPECIFIC SYNTHESES OF TRIFUNCTIONAL (R)-3-HYDROXY ESTERS BY BAKERS-YEAST REDUCTION
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[J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1983, (10) : 599 - 600
[10] ALDOL TYPE CONDENSATIONS OF BETA-KETO ESTER DIANIONS
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[J]. CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1974, 52 (11): : 2157 - 2164

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