| Literature DB >> 26986628 |
Galal Elgemeie1, Mamdouh Abu-Zaied2, Rasha Azzam1.
Abstract
A first synthesis of a new class of novel cytosine thioglycoside analogs from readily available starting materials has been described. The key step of this protocol is the formation of sodium pyrimidine-4-thiolate via condensation of N'-arylidene-2-cyanoacetohydrazides with sodium cyanocarbonimidodithioate salt, followed by coupling with halo sugars to give the corresponding cytosine thioglycoside analogs. Ammonolysis of the latter compounds afforded the free thioglycosides.Entities:
Keywords: N′-arylidene-2-cyanoacetohydrazides; antimetabolites; cyanocarbonimidodithioate salt; pyrimidine thioglycosides
Mesh:
Substances:
Year: 2016 PMID: 26986628 DOI: 10.1080/15257770.2015.1127961
Source DB: PubMed Journal: Nucleosides Nucleotides Nucleic Acids ISSN: 1525-7770 Impact factor: 1.381