Base-Modified Nucleosides: Etheno Derivatives

被引:29
|
作者
Jahnz-Wechmann, Zofia [1 ]
Framski, Grzegorz R. [1 ]
Januszczyk, Piotr A. [1 ]
Boryski, Jerzy [1 ]
机构
[1] Polish Acad Sci, Inst Bioorgan Chem, Poznan, Poland
来源
FRONTIERS IN CHEMISTRY | 2016年 / 4卷
关键词
nucleoside analogs; ethenonucleosides; wyosine; fused heterocycles; tricyclic acyclovir; antiviral activity; FLUORESCENT TRICYCLIC ANALOGS; ANTIVIRAL ACTIVITY; NUCLEIC-ACID; 3,5-CYCLIC PHOSPHATE; BIOLOGICAL-ACTIVITY; Y-NUCLEOSIDE; ACYCLOVIR; ADENOSINE; GANCICLOVIR; WYOSINE;
D O I
10.3389/fchem.2016.00019
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This review presents synthesis and chemistry of nucleoside analogs, possessing an additional fused, heterocyclic ring of the "etheno" type, such as 1,N-6-ethenoadenosine, 1,N-4-ethenocytidine, 1,N-2-ethenoguanosine, and other related derivatives. Formation of ethenonucleosides, in the presence of alpha-halocarbonyl reagents and their mechanism, stability, and degradation, reactions of substitution and transglycosylation, as well as their application in the nucleoside synthesis, have been described. Some of the discussed compounds may be applied as chemotherapeutic agents in antiviral and anticancer treatment, acting as pro-nucleosides of already known, biologically active nucleoside analogs.
引用
收藏
页数:10
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