Canadian Journal of Chemistry · 2006 · 13 citations · 10 references
Natural SciencesChemistryMedicinal ChemistryCatalysisNucleic Acid ChemistryOrganic ChemistryMicrowave-assisted SynthesisNucleic Acid SynthesisNucleobase ChemistryOrganic SynthesisMicrowave-assisted AlkylationMicrowave-assisted CatalysisMicrowave-assisted Green SynthesisMicrowave-assisted Organic SynthesisNucleobase SynthesisPurine ChemistryRegioselective SynthesisRegioselectivity
An efficient and green procedure for the synthesis of purine acyclic nucleosides through microwave-assisted alkylation of various purine nucleobases with 2-oxa-1,4-butanediol diacetate in the absence of solvent and catalyst is described. The advantages of using this method include its environmental friendliness, simple manipulation, short reaction time, high regioselectivity, and good yields.Key words: acyclic nucleosides, microwave irradiation, regioselectivity, alkylation, 2-oxa-1,4-butanediol diacetate.
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Novel substrate of adenosine deaminase
Howard J. Schaeffer, Shelly Gurwara, Robert Vince et al. · Journal of Medicinal Chemistry · 1971 · 84 citations
G. H. HAKIMELAHI, Tai Wei Ly, Ali Akbar Moosavi‐Movahedi et al. · Journal of Medicinal Chemistry · 2001 · 45 citations · Full text