SYNTHESIS OF (+/-) 1,2-DIDEOXY-1,2-DIAMINO-MYO-INOSITOL

被引：11

作者：

GUEDAT, P ^{[1
]}

SPIESS, B ^{[1
]}

SCHLEWER, G ^{[1
]}

机构：

[1] UNIV LOUIS PASTEUR STRASBOURG 1,FAC PHARM,CNRS,PHARMACOCHIM MOLEC LAB,F-67401 ILLKIRCH GRAFFENS,FRANCE

来源：

TETRAHEDRON LETTERS | 1994年 / 35卷 / 40期

关键词：

D O I：

10.1016/0040-4039(94)85318-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Starting from myo-inositol, an isostere. diaminated in positions 1 and 2, was prepared. The key step of the synthesis was the simultaneous inversion of the dimesylate 6 with sodium azide leading to the global retention of the configuration.

引用

页码：7375 / 7378

页数：4

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