STEREOSELECTIVE REDUCTION OF ALPHA-HYDROXY KETONES

被引：172

作者：

NAKATA, T ^{[1
]}

TANAKA, T ^{[1
]}

OISHI, T ^{[1
]}

机构：

[1] INST PHYS & CHEM RES,WAKO,SAITAMA 351,JAPAN

来源：

TETRAHEDRON LETTERS | 1983年 / 24卷 / 26期

关键词：

D O I：

10.1016/S0040-4039(00)87969-1

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：2653 / 2656

页数：4

共 12 条

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[2]

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[3]

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[4] STEREOSELECTIVITY IN REDUCTION OF ALIPHATIC ALPHA-KETOLS WITH ALUMINUM-HYDRIDE REAGENTS [J].

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BOWLUS, SB .

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[5] HIGHLY STEREOSELECTIVE SYNTHESIS OF ERYTHRO-ALPHA, BETA-EPOXY ALCOHOLS BY THE REDUCTION OF ALPHA, BETA-EPOXY KETONES WITH ZINC BOROHYDRIDE [J].

NAKATA, T ;

TANAKA, T ;

OISHI, T .

TETRAHEDRON LETTERS, 1981, 22 (47) :4723-4726

[6] STEREOSELECTIVE REDUCTION OF BETA-KETO-ESTERS WITH ZINC BOROHYDRIDE - STEREOSELECTIVE SYNTHESIS OF ERYTHRO-3-HYDROXY-2-ALKYLPROPIONATES [J].

NAKATA, T ;

OISHI, T .

TETRAHEDRON LETTERS, 1980, 21 (17) :1641-1644

[7] MARINE NATURAL-PRODUCTS FROM THE ATLANTIC ZONE .30. HIGHLY STEREOCONTROLLED REDUCTION OF ALPHA'-ALKOXYENONES TO GIVE EITHER THE THREO ORERYTHRO ALLYLIC 1,2-DIOL - ASSIGNMENT OF THE THREO CONFIGURATION TO THE C-15,C-16 DIOL OF PUMILIOTOXIN-B [J].

OVERMAN, LE ;

MCCREADY, RJ .

TETRAHEDRON LETTERS, 1982, 23 (23) :2355-2358

[8] STEREOSELECTIVE SYNTHESIS OF THE CHIRAL SEQUENCE OF ERYTHRONOLIDE-A [J].

STORK, G ;

PATERSON, I ;

LEE, FKC .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (17) :4686-4688

[9] THE STRUCTURE OF THE SIDE-CHAIN OF THE FROG ALKALOID PUMILIOTOXIN-B [J].

TOKUYAMA, T ;

SHIMADA, K ;

UEMURA, M .

TETRAHEDRON LETTERS, 1982, 23 (20) :2121-2124

[10]

WOWLUS SB, 1974, J ORG CHEM, V39, P3309

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