About: Pd-catalyzed Suzuki-Miyaura coupling reaction in the synthesis of 5-aryl-1-[2-(phosphonomethoxy)ethyl]uracils as potential multisubstrate inhibitors of thymidine phosphorylase     Goto   Sponge   NotDistinct   Permalink

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Description
  • 5-Aryl-1-[2-(phosphonomethoxy)ethyl]uracils were prepared via Pd-catalyzed Suzuki-Miyaura coupling reaction of the appropriate 5-bromouracil derivative with a series of arylboronic acids followed by deprotection. These compounds were designed as potential multisubstrate inhibitors of thymidine phosphorylase based on an assumption that the potential hydrophobic effect of the aryl groups might modify the inhibitory effect towards this enzyme and may also demonstrate cytostatic activity.
  • 5-Aryl-1-[2-(phosphonomethoxy)ethyl]uracils were prepared via Pd-catalyzed Suzuki-Miyaura coupling reaction of the appropriate 5-bromouracil derivative with a series of arylboronic acids followed by deprotection. These compounds were designed as potential multisubstrate inhibitors of thymidine phosphorylase based on an assumption that the potential hydrophobic effect of the aryl groups might modify the inhibitory effect towards this enzyme and may also demonstrate cytostatic activity. (en)
  • 5-Aryl-1-[2-(fosfonomethoxy)ethyl]uracily byly připraveny Pd-katalyzovanou Suzuki-Miyaura reakcí příslušného 5-bromuracilového derivátu s řadou arylboronových kyselin s nasledovanou deprotekcí. Tyto látky byly navrženy jako potenciální multisubstrátové inhibitory thymidinfosforylasy na základě předpokladu, že potenciální hydrofobní efekt arylové skupiny by mohl modifikovat inhibiční effekt vůči tomuto enzymu. (cs)
Title
  • Pd-catalyzed Suzuki-Miyaura coupling reaction in the synthesis of 5-aryl-1-[2-(phosphonomethoxy)ethyl]uracils as potential multisubstrate inhibitors of thymidine phosphorylase
  • Pd-catalyzed Suzuki-Miyaura coupling reaction in the synthesis of 5-aryl-1-[2-(phosphonomethoxy)ethyl]uracils as potential multisubstrate inhibitors of thymidine phosphorylase (en)
  • Pd-katalyzovaná Suzuki-Miyaura reakce v syntéze 5-aryl-1-[2-(fosfonomethoxy)ethyl]uracilů jako potenciálních inhibitorů thymidinfosforylasy (cs)
skos:prefLabel
  • Pd-catalyzed Suzuki-Miyaura coupling reaction in the synthesis of 5-aryl-1-[2-(phosphonomethoxy)ethyl]uracils as potential multisubstrate inhibitors of thymidine phosphorylase
  • Pd-catalyzed Suzuki-Miyaura coupling reaction in the synthesis of 5-aryl-1-[2-(phosphonomethoxy)ethyl]uracils as potential multisubstrate inhibitors of thymidine phosphorylase (en)
  • Pd-katalyzovaná Suzuki-Miyaura reakce v syntéze 5-aryl-1-[2-(fosfonomethoxy)ethyl]uracilů jako potenciálních inhibitorů thymidinfosforylasy (cs)
skos:notation
  • RIV/61388963:_____/07:00081288!RIV07-AV0-61388963
http://linked.open.../vavai/riv/strany
  • 3065;3067
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(1M0508), Z(AV0Z40550506)
http://linked.open...iv/cisloPeriodika
  • 17
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 440861
http://linked.open...ai/riv/idVysledku
  • RIV/61388963:_____/07:00081288
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • acyclic nucleoside phosphonates; thymidine phosphorylase; Suzuki coupling; pyrimidine (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [352F8730CB2D]
http://linked.open...i/riv/nazevZdroje
  • Tetrahedron Letters
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 48
http://linked.open...iv/tvurceVysledku
  • Holý, Antonín
  • Pohl, Radek
  • Pomeisl, Karel
http://linked.open...n/vavai/riv/zamer
issn
  • 0040-4039
number of pages
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