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  • An oxa-Michael addition of various secondary and branched primary alcohols to diethyl vinylphosphonate was studied and optimized. This efficient method precedes using of harsh reaction conditions and gains access to an important class of biologically active phosphonates in one step.
  • An oxa-Michael addition of various secondary and branched primary alcohols to diethyl vinylphosphonate was studied and optimized. This efficient method precedes using of harsh reaction conditions and gains access to an important class of biologically active phosphonates in one step. (en)
Title
  • An efficient oxa-Michael addition to diethyl vinylphosphonate under mild reaction conditions
  • An efficient oxa-Michael addition to diethyl vinylphosphonate under mild reaction conditions (en)
skos:prefLabel
  • An efficient oxa-Michael addition to diethyl vinylphosphonate under mild reaction conditions
  • An efficient oxa-Michael addition to diethyl vinylphosphonate under mild reaction conditions (en)
skos:notation
  • RIV/61388963:_____/12:00377462!RIV13-AV0-61388963
http://linked.open...avai/riv/aktivita
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  • P(VG20102015046), Z(AV0Z40550506)
http://linked.open...iv/cisloPeriodika
  • 4
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  • 121931
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  • RIV/61388963:_____/12:00377462
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  • oxa-Michael addition; secondary alcohols; diethyl vinylphosphonate (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
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  • [7E04A7A7672D]
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  • 2
http://linked.open...iv/tvurceVysledku
  • Baszczyňski, Ondřej
  • Dračínský, Martin
  • Janeba, Zlatko
  • Jansa, Petr
  • Špaček, Petr
  • Kaiser, Martin Maxmilian
http://linked.open...ain/vavai/riv/wos
  • 000299695300005
http://linked.open...n/vavai/riv/zamer
issn
  • 2046-2069
number of pages
http://bibframe.org/vocab/doi
  • 10.1039/c2ra00938b
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