Synthesis of New Bis-Alkylated Phosphono Alkenyl Acyclonucleosides : (Z) and (E)-Diethyl-2-(3-alkyl pyrimidin-1-yl)ethylen-1-yl Phosphonate

The E- and Z- phosphonoalkenyl acyclonucleosides of uracil and thymine were synthesized under Michael addition conditions. Introduction of an alkyl, alkenyl or alkynyl group at the N-3 position of the pyrimidine moiety was accomplished using potassium carbonate in DMF.

Bibliographic Details
Main Authors: J. L. Imbach, J. L. Barascut, H. B. Lazrek, M. Taourirte, A. Rochdi
Format: Article
Language:English
Published: MDPI AG 2000-10-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/5/10/1139/
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spelling doaj-694eee5d484f403bb95cfcd81bb8627e2020-11-24T20:41:34ZengMDPI AGMolecules1420-30492000-10-015101139114510.3390/51001139Synthesis of New Bis-Alkylated Phosphono Alkenyl Acyclonucleosides : (Z) and (E)-Diethyl-2-(3-alkyl pyrimidin-1-yl)ethylen-1-yl PhosphonateJ. L. ImbachJ. L. BarascutH. B. LazrekM. TaourirteA. RochdiThe E- and Z- phosphonoalkenyl acyclonucleosides of uracil and thymine were synthesized under Michael addition conditions. Introduction of an alkyl, alkenyl or alkynyl group at the N-3 position of the pyrimidine moiety was accomplished using potassium carbonate in DMF.http://www.mdpi.com/1420-3049/5/10/1139/AcyclonucleosidePhophonoalkenylMichael additionN-3-alkylation
collection DOAJ
language English
format Article
sources DOAJ
author J. L. Imbach
J. L. Barascut
H. B. Lazrek
M. Taourirte
A. Rochdi
spellingShingle J. L. Imbach
J. L. Barascut
H. B. Lazrek
M. Taourirte
A. Rochdi
Synthesis of New Bis-Alkylated Phosphono Alkenyl Acyclonucleosides : (Z) and (E)-Diethyl-2-(3-alkyl pyrimidin-1-yl)ethylen-1-yl Phosphonate
Molecules
Acyclonucleoside
Phophonoalkenyl
Michael addition
N-3-alkylation
author_facet J. L. Imbach
J. L. Barascut
H. B. Lazrek
M. Taourirte
A. Rochdi
author_sort J. L. Imbach
title Synthesis of New Bis-Alkylated Phosphono Alkenyl Acyclonucleosides : (Z) and (E)-Diethyl-2-(3-alkyl pyrimidin-1-yl)ethylen-1-yl Phosphonate
title_short Synthesis of New Bis-Alkylated Phosphono Alkenyl Acyclonucleosides : (Z) and (E)-Diethyl-2-(3-alkyl pyrimidin-1-yl)ethylen-1-yl Phosphonate
title_full Synthesis of New Bis-Alkylated Phosphono Alkenyl Acyclonucleosides : (Z) and (E)-Diethyl-2-(3-alkyl pyrimidin-1-yl)ethylen-1-yl Phosphonate
title_fullStr Synthesis of New Bis-Alkylated Phosphono Alkenyl Acyclonucleosides : (Z) and (E)-Diethyl-2-(3-alkyl pyrimidin-1-yl)ethylen-1-yl Phosphonate
title_full_unstemmed Synthesis of New Bis-Alkylated Phosphono Alkenyl Acyclonucleosides : (Z) and (E)-Diethyl-2-(3-alkyl pyrimidin-1-yl)ethylen-1-yl Phosphonate
title_sort synthesis of new bis-alkylated phosphono alkenyl acyclonucleosides : (z) and (e)-diethyl-2-(3-alkyl pyrimidin-1-yl)ethylen-1-yl phosphonate
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2000-10-01
description The E- and Z- phosphonoalkenyl acyclonucleosides of uracil and thymine were synthesized under Michael addition conditions. Introduction of an alkyl, alkenyl or alkynyl group at the N-3 position of the pyrimidine moiety was accomplished using potassium carbonate in DMF.
topic Acyclonucleoside
Phophonoalkenyl
Michael addition
N-3-alkylation
url http://www.mdpi.com/1420-3049/5/10/1139/
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AT jlbarascut synthesisofnewbisalkylatedphosphonoalkenylacyclonucleosideszandediethyl23alkylpyrimidin1ylethylen1ylphosphonate
AT hblazrek synthesisofnewbisalkylatedphosphonoalkenylacyclonucleosideszandediethyl23alkylpyrimidin1ylethylen1ylphosphonate
AT mtaourirte synthesisofnewbisalkylatedphosphonoalkenylacyclonucleosideszandediethyl23alkylpyrimidin1ylethylen1ylphosphonate
AT arochdi synthesisofnewbisalkylatedphosphonoalkenylacyclonucleosideszandediethyl23alkylpyrimidin1ylethylen1ylphosphonate
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