STEREOSELECTIVITY IN REDUCTION OF ALIPHATIC ALPHA-KETOLS WITH ALUMINUM-HYDRIDE REAGENTS

被引：66

作者：

KATZENEL.JA ^{[1
]}

BOWLUS, SB ^{[1
]}

机构：

[1] UNIV ILLINOIS, DEPT CHEM, ROGER ADAMS LAB, URBANA, IL 61801 USA

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1973年 / 38卷 / 04期

关键词：

D O I：

10.1021/jo00944a001

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：627 / 632

页数：6

共 38 条

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[3] SELECTIVE REDUCTIONS .X. REACTION OF ALUMINUM HYDRIDE WITH SELECTED ORGANIC COMPOUNDS CONTAINING REPRESENTATIVE FUNCTIONAL GROUPS . COMPARISON OF REDUCING CHARACTERISTICS OF LITHIUM ALUMINUM HYDRIDE AND ITS DERIVATIVES
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[J]. AUSTRALIAN JOURNAL OF CHEMISTRY, 1969, 22 (10) : 2145 - &
[6] CHEREST M, 1968, TETRAHEDRON LETT, P2205
[7] ALICYCLIC GLYCOLS .1. TOLUENE-PARA-SULPHONYL AND METHANESULPHONYL DERIVATIVES OF CYCLOHEXANE-1-2-DIOL
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[8] OXIDATION OF EPOXIDES BY DIMETHYL SULFOXIDE - A SIMPLE SYNTHESIS OF ALPHA-HYDROXY KETONES
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[J]. JOURNAL OF ORGANIC CHEMISTRY, 1961, 26 (05) : 1681 - &
[9] STEREOSPECIFIC SYNTHESES OF OLEFINS FROM 1,2-THIONOCARBONATES AND 1,2-TRITHIOCARBONATES . TRANS-CYCLOHEPTENE
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1965, 87 (04) : 934 - &
[10] A NEW, STEREOSPECIFIC OLEFIN SYNTHESIS FROM 1,2-DIOLS
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