Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Julie Risse"'
Publikováno v:
Zeitschrift für anorganische und allgemeine Chemie. 640:1322-1329
The dimeric ruthenium complex [Cp^RuCl2](2) is easily accessible in a one-pot reaction from RuCl3(solv)(n) and tert-butylacetylene. It features sterically very demanding "Cp-roof" ligands (Cp^ = eta(5)-1-methoxy-2,4-tert-butyl-3-neopentylcyclopentadi
Publikováno v:
European Journal of Inorganic Chemistry. 2013:4558-4562
The dinuclear complexes [(p-cymene)RuCl2]2 and [(cyclopentadienyl)MCl2]2 (M = Ru, Rh, Ir) are important starting materials in organometallic chemistry. The standard synthesis of these complexes involves heating of an alcoholic solution of RuIII, RhII
Autor:
Olivier Zava, Albert Ruggi, Frédéric Schmitt, Christian G. Hartinger, Wee Han Ang, Julie Risse, Lucienne Juillerat-Jeanneret, Alexey A. Nazarov, Paul J. Dyson, Rosario Scopelitti, Michael Groessl
Publikováno v:
Inorganic Chemistry. 51:3633-3639
Anthracene derivatives of ruthenium(II) arene compounds with 1,3,5-triaza-7-phosphatricyclo[3.3.1.1]decane (pta) or a sugar phosphite ligand, viz., 3,5,6-bicyclophosphite-1,2-O-isopropylidene-α-d-glucofuranoside, were prepared in order to evaluate t
Publikováno v:
Organometallics. 30:3412-3418
The cyclopentadienyl Ru complexes Cp*RuCl(cod) (cod = 1,5-cyclooctadiene), Cp*RuCl(PPh3)2, and [Cp∧RuCl2]2 (Cp∧ = η5-1-methoxy-2,4-di-tert-butyl-3-neopentylcyclopentadienyl) are able to catalyze the decomposition of benzyl azides to give 1,3,5-t
Publikováno v:
ChemInform. 43
A two-step process for the synthesis of trifluoromethyl-substituted cyclopropanes is described. Halothane, an anesthetic agent, is added to olefins in a ruthenium-catalyzed Kharasch reaction. The resulting 1,3-dihalides are converted into cyclopropan
Publikováno v:
Organometallics; Jun2011, Vol. 30 Issue 12, p3412-3418, 7p
A two-step process for the synthesis of trifluoromethyl-substituted cyclopropanes is described. Halothane, an anesthetic agent, is added to olefins in a ruthenium-catalyzed Kharasch reaction. The resulting 1,3-dihalides are converted into cyclopropan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6e84240f0e82cd6f6ffc913a1f5d660
https://infoscience.epfl.ch/record/178380
https://infoscience.epfl.ch/record/178380