An improved approach to the synthesis of adenosine-5'-N-ethyluronamides of interest as adenosine receptor agonists

被引：12

作者：

Ha, SB ^{[1
]}

Nair, V ^{[1
]}

机构：

[1] UNIV IOWA,DEPT CHEM,IOWA CITY,IA 52242

来源：

TETRAHEDRON LETTERS | 1996年 / 37卷 / 10期

关键词：

D O I：

10.1016/0040-4039(96)00092-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Adenosine-5'-N-ethyluronamides which are modified at the 6-amino group are of considerable interest as adenosine receptor agonists. This report describes a new and efficient approach to the synthesis of this class of biologically active compounds.

引用

页码：1567 / 1570

页数：4

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