| Literature DB >> 26398890 |
Galal Elgemeie1, Mamdouh Abu-Zaied2.
Abstract
A first microwave-assisted synthesis of a new class of novel purine thioglycoside analogues from readily available starting materials has been described. The key step of this protocol is the formation of sodium pyrazolo[1,5-a][1,3,5]triazine-4-thiolates via condensation of 5-amino-1H-pyrazoles with sodium cyanocarbonimidodithioate salt under microwave irradiation, followed by coupling with halo sugars to give the corresponding purine thioglycoside analogues. Further studies on the application of this method for the synthesis of other highly functionalized biologically active glycosides are underway.Entities:
Keywords: Microwave synthesis; anti-metabolites; purine thioglycoside analogues; sodium cyanocarbonimidodithioate salt; thioglycosides
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Year: 2015 PMID: 26398890 DOI: 10.1080/15257770.2015.1078470
Source DB: PubMed Journal: Nucleosides Nucleotides Nucleic Acids ISSN: 1525-7770 Impact factor: 1.381