Synthesis of 2H-azolo[1,5-a][1,2,3]triazolo[4,5-e]pyrimidines

被引：7
|
作者：
Gorbunov, Evgeny B. [1 ,2 ]
Rusinov, Gennady L. [1 ,2 ]
Ulomskii, Evgeny N. [1 ,2 ]
Isenov, Maksim L. [1 ]
Charushin, Valery N. [1 ,2 ]
机构：
[1] Russian Acad Sci, I Ya Postovskii Inst Organ Synth, Ural Branch, Ekaterinburg 620990, Russia
[2] Ural Fed Univ, Ekaterinburg 620002, Russia
来源：
CHEMISTRY OF HETEROCYCLIC COMPOUNDS | 2015年 / 51卷 / 05期
基金：
俄罗斯基础研究基金会; 俄罗斯科学基金会;
关键词：
azapurines; 6-nitroazolo[1,5-alpha]pyrimidines; catalytic hydrogenation; 1,3-dipolar cycloaddition; A(1) ADENOSINE RECEPTORS; CARBOCYCLIC NUCLEOSIDES; INHIBITORS; ANALOGS; DESIGN; IDENTIFICATION; ANTAGONISTS; DEAMINASE;
D O I：
10.1007/s10593-015-1725-2
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
6-Nitroazolo[1,5-a]pyrimidines were used as dipolarophiles in a reaction with sodium azide providing previously unknown 2De-azolo[1,5-a]-[1,2,3]triazolo[4,5-e]pyrimidines.
引用
收藏
页码：491 / 495
页数：5
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