ACYCLIC STEREOSELECTION .43. STEREOSELECTIVE SYNTHESIS OF THE C-8 TO C-15 MOIETY OF ERYTHRONOLIDE-A

被引：21

作者：

HOAGLAND, S ^{[1
]}

MORITA, Y ^{[1
]}

BAI, DL ^{[1
]}

MARKI, HP ^{[1
]}

KEES, K ^{[1
]}

BROWN, L ^{[1
]}

HEATHCOCK, CH ^{[1
]}

机构：

[1] UNIV CALIF BERKELEY,DEPT CHEM,BERKELEY,CA 94720

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1988年 / 53卷 / 20期

关键词：

D O I：

10.1021/jo00255a013

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：4730 / 4735

页数：6

共 11 条

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[5] ACYCLIC STEREOSELECTION .23. LACTALDEHYDE ENOLATE EQUIVALENTS
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[8] DIASTEREOSELECTIVE AND ENANTIOSELECTIVE PREPARATION OF BETA-ALKYLHOMOALLYLIC ALCOHOLS - SYNTHESIS OF SERRICORNIN AND CORYNOMYCOLIC ACID
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[9] ASYMMETRIC EPOXIDATION PROVIDES SHORTEST ROUTES TO 4 CHIRAL EPOXY ALCOHOLS WHICH ARE KEY INTERMEDIATES IN SYNTHESES OF METHYMYCIN, ERYTHROMYCIN, LEUKOTRIENE C-1, AND DISPARLURE
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