TOTAL SYNTHESIS AND ABSOLUTE STEREOCHEMISTRY OF THE ANTIFUNGAL DIPEPTIDE SCH 37137 AND ITS 2S,3S-ISOMER

被引：38

作者：

RANE, DF ^{[1
]}

GIRIJAVALLABHAN, VM ^{[1
]}

GANGULY, AK ^{[1
]}

PIKE, RE ^{[1
]}

SAKSENA, AK ^{[1
]}

MCPHAIL, AT ^{[1
]}

机构：

[1] DUKE UNIV,DEPT CHEM,DURHAM,NC 27708

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 20期

关键词：

D O I：

10.1016/S0040-4039(00)73660-4

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The absolute stereochemistry of the epoxide moiety in Sch 37137 has been established as 2R, 3R by its synthesis from L-tartaric acid.

引用

页码：3201 / 3204

页数：4

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