Easy and stereoselective synthesis of the phosphono analogue of alpha-L-rhamnose 1-phosphate

被引：10

作者：

Cipolla, L ^{[1
]}

LaFerla, B ^{[1
]}

Nicotra, F ^{[1
]}

Panza, L ^{[1
]}

机构：

[1] UNIV MILAN,DIPARTIMENTO CHIM ORGAN & IND,CNR,CTR STUDIO SOSTANZE ORGAN NAT,I-20133 MILAN,ITALY

来源：

TETRAHEDRON LETTERS | 1997年 / 38卷 / 31期

关键词：

D O I：

10.1016/S0040-4039(97)01245-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The C-glycosidic analogue of alpha-L-rhamnose I-phosphate has been stereoselectively synthesised reacting 2,3,4-tri-O-benzyl-L-rhamnopyranose with tetraethyl methylenediphosphonate and sodium hydride in diglyme, and then deprotecting with iodotrimethylsilane. (C) 1997 Published by Elsevier Science Ltd.

引用

页码：5567 / 5568

页数：2

共 5 条

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[5] CARDIAC-GLYCOSIDES .7. SUGAR STEREOCHEMISTRY AND CARDIAC GLYCOSIDE ACTIVITY
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