An Efficient Protocol for the Synthesis of Carboacyclic Nucleosides via Aza-Conjugate Addition Reaction
A new efficient method for the synthesis of carboacyclic nucleosides as biologically interesting compounds via aza-conjugate addition of pyrimidine nucleobases to a,β-unsaturated esters in the presence of catalytic amount of LiOH.H2O (1.2-4.8 mol%) under microwave irradiation is described. This meth...
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Iranian Institute of Research and Development in Chemical Industries (IRDCI)-ACECR
2010-12-01
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doaj-e738b1f479ef4c08803f9319ea6c581c2020-11-25T02:54:03ZengIranian Institute of Research and Development in Chemical Industries (IRDCI)-ACECRIranian Journal of Chemistry & Chemical Engineering 1021-99861021-99862010-12-0129467736406An Efficient Protocol for the Synthesis of Carboacyclic Nucleosides via Aza-Conjugate Addition ReactionMohammad Ali Zolfigol0Ardeshir Khazaei1Ahmad Reza Moosavi-Zare2Abdolkarim Zare3Ali Reza Hasanijejad4Faculty of Chemistry, Bu-Ali Sina University, Hamedan, I.R. IRANFaculty of Chemistry, Bu-Ali Sina University, Hamedan, I.R. IRANFaculty of Chemistry, Bu-Ali Sina University, Hamedan, I.R. IRANDepartment of Chemistry, Payame Noor University (PNU), Tehran, I.R. IRANDepartment of Chemistry, Faculty of Sciences, Persian Gulf University, Bushehr, I.R. IRANA new efficient method for the synthesis of carboacyclic nucleosides as biologically interesting compounds via aza-conjugate addition of pyrimidine nucleobases to a,β-unsaturated esters in the presence of catalytic amount of LiOH.H2O (1.2-4.8 mol%) under microwave irradiation is described. This method affords the title compounds in good to excellent yields and in short reaction times.http://www.ijcce.ac.ir/article_6406_af1dd59e7f68c78ceed0b21ff2e77e8b.pdfcarboacyclic nucleosideaza-conjugate addition reactionpyrimidine nucleobase-unsaturated estermicrowave |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mohammad Ali Zolfigol Ardeshir Khazaei Ahmad Reza Moosavi-Zare Abdolkarim Zare Ali Reza Hasanijejad |
spellingShingle |
Mohammad Ali Zolfigol Ardeshir Khazaei Ahmad Reza Moosavi-Zare Abdolkarim Zare Ali Reza Hasanijejad An Efficient Protocol for the Synthesis of Carboacyclic Nucleosides via Aza-Conjugate Addition Reaction Iranian Journal of Chemistry & Chemical Engineering carboacyclic nucleoside aza-conjugate addition reaction pyrimidine nucleobase -unsaturated ester microwave |
author_facet |
Mohammad Ali Zolfigol Ardeshir Khazaei Ahmad Reza Moosavi-Zare Abdolkarim Zare Ali Reza Hasanijejad |
author_sort |
Mohammad Ali Zolfigol |
title |
An Efficient Protocol for the Synthesis of Carboacyclic Nucleosides via Aza-Conjugate Addition Reaction |
title_short |
An Efficient Protocol for the Synthesis of Carboacyclic Nucleosides via Aza-Conjugate Addition Reaction |
title_full |
An Efficient Protocol for the Synthesis of Carboacyclic Nucleosides via Aza-Conjugate Addition Reaction |
title_fullStr |
An Efficient Protocol for the Synthesis of Carboacyclic Nucleosides via Aza-Conjugate Addition Reaction |
title_full_unstemmed |
An Efficient Protocol for the Synthesis of Carboacyclic Nucleosides via Aza-Conjugate Addition Reaction |
title_sort |
efficient protocol for the synthesis of carboacyclic nucleosides via aza-conjugate addition reaction |
publisher |
Iranian Institute of Research and Development in Chemical Industries (IRDCI)-ACECR |
series |
Iranian Journal of Chemistry & Chemical Engineering |
issn |
1021-9986 1021-9986 |
publishDate |
2010-12-01 |
description |
A new efficient method for the synthesis of carboacyclic nucleosides as biologically interesting compounds via aza-conjugate addition of pyrimidine nucleobases to a,β-unsaturated esters in the presence of catalytic amount of LiOH.H2O (1.2-4.8 mol%) under microwave irradiation is described. This method affords the title compounds in good to excellent yields and in short reaction times. |
topic |
carboacyclic nucleoside aza-conjugate addition reaction pyrimidine nucleobase -unsaturated ester microwave |
url |
http://www.ijcce.ac.ir/article_6406_af1dd59e7f68c78ceed0b21ff2e77e8b.pdf |
work_keys_str_mv |
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