Green Chemistry · 2012 · 18 citations · 20 references
Natural SciencesChemistryMedicinal ChemistryCatalysisGreen ChemistryOrganic ChemistryHeterocycle SynthesisHeterocyclic ChemistryNucleic Acid SynthesisNucleobase ChemistryOrganic SynthesisSolvent-free SynthesisCatalyst-free Solvent-free ReactionsNucleobase SynthesisNucleoside Analog SynthesisNucleoside AnalogsPurine AnaloguesPurine ChemistrySolvent-free CatalysisSolvent-free Processing
C6-azolyl purine nucleoside products are prepared in high yields under solvent- and catalyst-free conditions via C–N coupling reaction of unprotected 6-chloropurine nucleosides and N-heterocycles, providing a unifying, simple and environmentally friendly complement to the available methods.
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Travis T. Denton, Xiaodong Zhang, John R. Cashman · Journal of Medicinal Chemistry · 2004 · 144 citations · Full text
Jiangqiong Liu, Morris J. Robins · Organic Letters · 2004 · 109 citations