STEREOCHEMICAL STUDIES OF EPOXIDES RELEVANT TO THE ANSA CHAIN OF THE STREPTOVARICINS

被引：40

作者：

WANG, ZY

SCHREIBER, SL

机构：

[1] Department of Chemistry, Yale University New Haven

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 01期

关键词：

D O I：

10.1016/S0040-4039(00)94326-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：31 / 34

页数：4

共 17 条

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[6] SYNTHESIS OF A KEY INTERMEDIATE FOR THE TOTAL SYNTHESIS OF STREPTOVARICIN-A
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[7] DIASTEREOFACIAL SELECTIVITY OF ENOLATES
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[8] VANADIUM-CATALYZED EPOXIDATIONS .2. HIGHLY STEREOSELECTIVE EPOXIDATIONS OF ACYCLIC HOMOALLYLIC ALCOHOLS PREDICTED BY A DETAILED TRANSITION-STATE MODEL
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[9] STEREOCONTROLLED SYNTHESIS OF D-PENTITOLS, 2-AMINO-2-DEOXY-D-PENTITOLS, AND 2-DEOXY-D-PENTITOLS FROM D-GLYCERALDEHYDE ACETONIDE
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (04) : 1109 - 1111
[10] PYRANOSIDIC HOMOLOGATION .11. COMPLEMENTARY ROUTES TO REMOTE TERTIARY ALCOHOLS OF STREPTOVARICIN-A
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[J]. JOURNAL OF ORGANIC CHEMISTRY, 1987, 52 (20) : 4511 - 4517

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