Enantioselective desymmetrisation of achiral epoxides

被引：350

作者：

Hodgson, DM

Gibbs, AR

Lee, GP

机构：

[1] Dyson Perrins Laboratory, University of Oxford, Oxford OX1 3QY, South Parks Road

来源：

TETRAHEDRON | 1996年 / 52卷 / 46期

关键词：

CHIRAL LITHIUM AMIDE; CYCLOHEXENE OXIDE; MESO-EPOXIDES; ASYMMETRIC-SYNTHESIS; SYMMETRICAL EPOXIDES; ALLYLIC ALCOHOLS; TRIMETHYLSILYL AZIDE; KINETIC RESOLUTION; DEPROTONATION; BASES;

D O I：

10.1016/0040-4020(96)00888-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

[No abstract available]

引用

页码：14361 / 14384

页数：24

共 91 条

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[3] RECONFIRMATION OF HIGH ENANTIOMERIC EXCESSES IN THE ENANTIOSELECTIVE TRANSFORMATION OF MESO-EPOXIDES
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[8] AN ASYMMETRIC-SYNTHESIS OF CIS-4-TERT-BUTYLDIMETHYLSILOXY-2-CYCLOPENTEN-1-OL AND CIS-4-TETRAHYDROPYRANYLOXY-2-CYCLOPENTEN-1-OL, VERSATILE CHIRAL SYNTHETIC INTERMEDIATE FOR PROSTANOIDS
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[9] A KINETIC RESOLUTION OF RACEMIC EPOXIDES BY A CHIRAL LITHIUM AMIDE
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[10] Asymmetric transformation of meso-epoxides by chiral lithium amides
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