Phosphonate analogues of nucleoside polyphosphates

被引:3
|
作者
Romanenko, Vadim D. [1 ]
Kukhar, Valery P. [1 ]
机构
[1] Natl Acad Sci Ukraine, Inst Bioorgan Chem & Petrochem, Murmanska St 1, UA-02660 Kiev, Ukraine
关键词
Pyrophosphate analogues; modified nucleotides; bisphosphonates; multicomponent reactions; phosphonate carbanions; HIV-1; REVERSE-TRANSCRIPTASE; DNA-POLYMERASE-BETA; URACIL NUCLEOTIDE DERIVATIVES; CYCLIC ADP-RIBOSE; TRIPHOSPHATE ANALOGS; EFFICIENT SYNTHESIS; METHYLENE ANALOGS; CAP ANALOGS; ATP ANALOGS; METHYLENEBISPHOSPHONATE LINKAGE;
D O I
10.24820/ark.5550190.p010.183
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
This article provides an overview of the efforts toward the synthesis of nucleoside polyphosphate mimics featuring a P-CXY-P scaffold. The following synthetic approaches to these compounds are summarized: (i) nucleophilic displacement of 5'-O-tosyl nucleoside by the ammonium salts of methylenebisphosphonic acid; (ii) synthesis via activated phosphate/phosphonate substrates; (iii) Mitsunobu coupling between a nucleoside and methylenebisphosphonic acid; (iv) phosphorylation of a protected nucleoside under Yoshikawa's reaction conditions with methylenebis(phosphonic dichloride); (v) synthesis via nucleophilic cleavage of cyclic trimetaphosph(on) ates; (vi) enzyme-mediated reactions.
引用
收藏
页码:1 / 49
页数:49
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