ENANTIOSELECTIVE SYNTHESIS OF (R)-(-)-1-PHENYLETHANOLAMINES USING BAKERS-YEAST REDUCTION OF SOME ALPHA-SUBSTITUTED METHYL PHENYL KETONES

被引：0

作者：

BRENELLI, ECS ^{[1
]}

DECARVALHO, M ^{[1
]}

OKUBO, MT ^{[1
]}

MARQUES, M ^{[1
]}

MORAN, PJS ^{[1
]}

RODRIGUES, JAR ^{[1
]}

SORRILHA, AEPM ^{[1
]}

机构：

[1] UNIV ESTADUAL CAMPINAS,INST QUIM,BR-13081-970 CAMPINAS,BRAZIL

来源：

INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY | 1992年 / 31卷 / 12期

关键词：

D O I：

暂无

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The Baker's yeast reductions of alpha-chloroacetophenone, alpha-azidoacetophenone and 2-oxo-2-phenylacetamide are used as key steps in the preparation of optically active (R)-(-)-1-phenylethanolamines.

引用

页码：821 / 823

页数：3

共 28 条

[21] SYNTHESIS OF OPTICALLY-ACTIVE T-BUTYL (3R,5S)-3,5-ISOPROPYLIDENEDIOXY-6-HEPTYNOATE THROUGH BAKERS-YEAST REDUCTION OF METHYL 3-OXO-4-PENTYNOATE
ANSARI, MH
KUSUMOTO, T
HIYAMA, T
TETRAHEDRON LETTERS, 1993, 34 (51) : 8271 - 8274
[22] PREPARATION AND ASSIGNMENT OF CONFIGURATION OF 1-BENZOYL-(2S)-TERT-BUTYL-3-METHYL-PERHYDROPYRIMIDIN-4-ONE - USEFUL STARTING MATERIAL FOR THE ENANTIOSELECTIVE SYNTHESIS OF ALPHA-SUBSTITUTED BETA-AMINO ACIDS
JUARISTI, E
QUINTANA, D
TETRAHEDRON-ASYMMETRY, 1992, 3 (06) : 723 - 726
[23] A FACILE SYNTHESIS OF OPTICALLY PURE L-ARMENTOMYCIN AND ITS D-ISOMER - HIGHLY ENANTIOSELECTIVE REDUCTION OF THE C-C DOUBLE-BOND OF METHYL (E)-2,4,4-TRICHLORO-2-BUTENOATE AND (Z)-2,4,4-TRICHLORO-2-BUTENOATE BY USING BAKERS-YEAST
UTAKA, M
KONISHI, S
OKUBO, T
TSUBOI, S
TAKEDA, A
TETRAHEDRON LETTERS, 1987, 28 (13) : 1447 - 1450
[24] SYNTHESIS OF THE 4 CONFIGURATIONAL ISOMERS OF N-BENZOYL-2,3,6-TRIDEOXY-3-C-METHYL-3-AMINO-L-HEXOSE FROM THE (2S,3R)-DIOL OBTAINED FROM ALPHA-METHYLCINNAMALDEHYDE BY FERMENTATION WITH BAKERS-YEAST
FRONZA, G
FUGANTI, C
GRASSELLI, P
PEDROCCHIFANTONI, G
JOURNAL OF CARBOHYDRATE CHEMISTRY, 1983, 2 (03) : 225 - 248
[25] NOVEL CHIRAL BUILDING BLOCK - (2R,3S)-2-(1,3-DITHIAN-2-YL)-3-HYDROXYBUTANOATES - HIGHLY DIASTEREOSELECTIVE AND ENANTIOSELECTIVE BAKERS-YEAST REDUCTION OF 2-(1,3-DITHIAN-2-YL)-3-OXOBUTANOATES
CHIKASHITA, H
MOTOZAWA, T
ITOH, K
SYNTHETIC COMMUNICATIONS, 1989, 19 (5-6) : 1119 - 1124
[26] Synthesis of chiral alpha-substituted N-[((2S)-2-hydroxy-2-phenyl)-ethyl]-2-phenylglycine derivatives by diastereocontrolled alkylation of (6R)-2,3,5,6-tetrahydro-3,6-diaryl-N-[(2'R)-(2'-methyl)phenyl-methyl]-4H-1,4-oxazin-2-ones
Remuzon, P
Soumeillant, M
Dussy, C
Bouzard, D
TETRAHEDRON, 1997, 53 (52) : 17711 - 17726
[27] Synthesis and 1H and 13C NMR spectral study of some r(2),c(4)-bis(isopropylcarbonyl)-c(5)-hydroxy-t(5)-methyl-t(3)-substituted phenyl, cyclohexanones and their oximes
Balachander, R.
Sameera, S. A.
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JOURNAL OF MOLECULAR STRUCTURE, 2016, 1115 : 63 - 69
[28] Synthesis of the (1S,2S)- and (1R,2S)-stereoisomers of the respective E- and Z-isomers of ethyl 4-[(2-hydroxycyclohexyl)methyllphenoxy-3-methyl-2-butenoate using yeast whole cell bioreduction of the parent ketones
Wimmer, Z
Saman, D
Zarevúcka, M
Wimmerová, M
TETRAHEDRON-ASYMMETRY, 2005, 16 (16) : 2810 - 2815

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