About: The efficient synthesis of 2-arylpyrimidine acyclic nucleoside phosphonates using Liebeskind-Srogl cross-coupling reaction     Goto   Sponge   NotDistinct   Permalink

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Description
  • A series of novel acyclic nucleoside phosphonates with various aryls attached to the C-2 position of the pyrimidine moiety has been prepared using the Liebeskind-Srogl cross-coupling protocol. The reactions of highly functionalised 2-(methylsulfanyl)pyrimidines with various arylboronic acids were studied and optimised.
  • A series of novel acyclic nucleoside phosphonates with various aryls attached to the C-2 position of the pyrimidine moiety has been prepared using the Liebeskind-Srogl cross-coupling protocol. The reactions of highly functionalised 2-(methylsulfanyl)pyrimidines with various arylboronic acids were studied and optimised. (en)
Title
  • The efficient synthesis of 2-arylpyrimidine acyclic nucleoside phosphonates using Liebeskind-Srogl cross-coupling reaction
  • The efficient synthesis of 2-arylpyrimidine acyclic nucleoside phosphonates using Liebeskind-Srogl cross-coupling reaction (en)
skos:prefLabel
  • The efficient synthesis of 2-arylpyrimidine acyclic nucleoside phosphonates using Liebeskind-Srogl cross-coupling reaction
  • The efficient synthesis of 2-arylpyrimidine acyclic nucleoside phosphonates using Liebeskind-Srogl cross-coupling reaction (en)
skos:notation
  • RIV/61388963:_____/11:00363154!RIV12-AV0-61388963
http://linked.open...avai/riv/aktivita
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  • P(1M0508), Z(AV0Z40550506)
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  • 38
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  • 196766
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  • RIV/61388963:_____/11:00363154
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  • Liebeskind-Srogl cross-coupling; acyclic nucleoside phosphonates; pyrimidines; arylboronic acids; microwave (en)
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  • GB - Spojené království Velké Británie a Severního Irska
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  • [65425F34EE14]
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  • Tetrahedron
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  • 67
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  • Dračínský, Martin
  • Holý, Antonín
  • Janeba, Zlatko
  • Břehová, Petra
  • Česnek, Michal
http://linked.open...ain/vavai/riv/wos
  • 000294593400026
http://linked.open...n/vavai/riv/zamer
issn
  • 0040-4020
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.tet.2011.07.040
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