About: The role of the aromatic ligand in the asymmetric transfer hydrogenation of the CN double bond; length as m-dashN bond on Noyori's chiral Ru catalysts     Goto   Sponge   NotDistinct   Permalink

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Description
  • Only four types of dimeric precursors [RuCl2(éta6-arene)]2 for the synthesis of Noyori's half sandwich diamine catalysts [RuCl(TsDPEN)(éta6-arene)] are commercially available, yet so far no study has tried to systematically evaluate how these systems perform during the asymmetric transfer hydrogenation of various 3,4-dihydroisoquinolines (i.e., the typical substrates for Noyori asymmetric transfer hydrogenation benchmarking). Experiments combined with molecular modeling allowed us to assess their properties and formulate a hypothesis clarifying the difference in enantioselectivity of these systems.
  • Only four types of dimeric precursors [RuCl2(éta6-arene)]2 for the synthesis of Noyori's half sandwich diamine catalysts [RuCl(TsDPEN)(éta6-arene)] are commercially available, yet so far no study has tried to systematically evaluate how these systems perform during the asymmetric transfer hydrogenation of various 3,4-dihydroisoquinolines (i.e., the typical substrates for Noyori asymmetric transfer hydrogenation benchmarking). Experiments combined with molecular modeling allowed us to assess their properties and formulate a hypothesis clarifying the difference in enantioselectivity of these systems. (en)
Title
  • The role of the aromatic ligand in the asymmetric transfer hydrogenation of the CN double bond; length as m-dashN bond on Noyori's chiral Ru catalysts
  • The role of the aromatic ligand in the asymmetric transfer hydrogenation of the CN double bond; length as m-dashN bond on Noyori's chiral Ru catalysts (en)
skos:prefLabel
  • The role of the aromatic ligand in the asymmetric transfer hydrogenation of the CN double bond; length as m-dashN bond on Noyori's chiral Ru catalysts
  • The role of the aromatic ligand in the asymmetric transfer hydrogenation of the CN double bond; length as m-dashN bond on Noyori's chiral Ru catalysts (en)
skos:notation
  • RIV/60461373:22310/14:43897968!RIV15-GA0-22310___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GAP106/12/1276)
http://linked.open...iv/cisloPeriodika
  • 18-19
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
  • 43197
http://linked.open...ai/riv/idVysledku
  • RIV/60461373:22310/14:43897968
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • arene; imines; ruthenium (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • IE - Irsko
http://linked.open...ontrolniKodProRIV
  • [7DF235B92537]
http://linked.open...i/riv/nazevZdroje
  • Tetrahedron Asymmetry
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
  • 25
http://linked.open...iv/tvurceVysledku
  • Kačer, Petr
  • Kuzma, Marek
  • Václavík, Jiří
  • Vilhanová, Beáta
  • Pecháček, Jan
  • Zápal, Jakub
  • Šot, Petr
http://linked.open...ain/vavai/riv/wos
  • 000343847700014
issn
  • 0957-4166
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.tetasy.2014.08.011
http://localhost/t...ganizacniJednotka
  • 22310
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