Microwave-assisted regioselective synthesis of acyclic nucleosides through an alkylating reaction with 2-oxa-1,4-butanediol diacetate

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...

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Veröffentlicht in:Canadian journal of chemistry 2006-05, Vol.84 (5), p.819-824
Hauptverfasser: Qu, Guirong, Han, Suhui, Zhang, Zhiguang, Geng, Mingwei, Xue, Feng
Format: Artikel
Sprache:eng
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Zusammenfassung: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.
ISSN:0008-4042
1480-3291
DOI:10.1139/v06-061