Highly efficient synthesis of carboacyclic nucleosides catalyzed by zinc oxide in 1-butyl-3-methylimidazolium bromide (ZnO/[bmim]Br)

Iranian Journal of Catalysis

مقاله 12، دوره 4، شماره 4، اسفند 2014، صفحه 295-303   

نوع مقاله: Articles

نویسندگان

Tarlan Salehi-Hamzehkhani¹؛ Marzieh Hatami¹؛ Abdolkarim Zare^{* 1}؛ Ahmad Reza Moosavi-Zare²؛ Abolfath Parhami¹؛ Zahra Khedri¹؛ Hamideh Kabgani¹؛ Mohammad Beikagha¹؛ Raheleh Salamipoor¹

¹Department of Chemistry, Payame Noor University, P.O. Box 19395-3697, Tehran, Iran.

²Department of Chemistry, University of Sayyed Jamaleddin Asadabadi, Asadabad, 6541835583, Iran.

چکیده

Michael addition of pyrimidine and purine nucleobases to substituted as well as unsubstituted α,β-unsaturated esters efficiently proceeds in the presence of catalytic amount of zinc oxide in ionic liquid 1-butyl-3-methylimidazolium bromide (ZnO/[bmim]Br) under microwave irradiation to afford carboacyclic nucleosides, as biologically important compounds, in good to excellent yields and in short reaction times.

کلیدواژه‌ها

Carboacyclic nucleoside؛ Michael addition؛ Zinc oxide؛ Ionic Liquid؛ 1-Butyl-3-methylimidazolium bromide ([bmim]Br)؛ Microwave irradiation

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