Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Dichlorotris(triphenylphosphine)ruthenium(II)"'
Autor:
José Luiz Silva Sá, José Antônio de Sousa, Luciano T. Costa, Benedito dos Santos Lima Neto, Mayrla Letícia Alves de Oliveira, Francisco das Chagas Alves Lima, José Walkimar de M. Carneiro
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
The structure and substitution energies of dichlorotris(triphenylphosphine)ruthenium(II) complex, [RuCl2(PPh3)3], was computed with ten different methods at the density functional theory level usin...
Publikováno v:
Molecular Catalysis. 490:110970
The complex RuCl2(PPh3)3 (1) showed to be an efficient and regioselective precatalyst for the hydrogenation of quinoline (Q) to 1,2,3,4-tetrahydroquinoline (THQ) at P = 5.0–6.5 at m and T = 140−167 °C. This reaction showed to be first order on c
Publikováno v:
Macromolecules. 32:4769-4775
3-Aminopropyl-functionalized silica support (APSS) has been used as a solid support for the heterogeneous atom transfer polymerization of methyl methacrylate (MMA), to poly(methyl methacrylate) (PMMA), mediated by adsorbed RuCl2(PPh3)3 as catalyst. T
Publikováno v:
Fieser and Fieser's Reagents for Organic Synthesis
This article has no abstract. Keywords: use; reduction of cyclic anhydrides; selective hydrogenations; hydrogenation of aldehydes; claisen rearrangement of diallyl ethers; γ-butyrolactones; tertiary amines; selective oxidation of alcohols; N-alkylat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e5c8883a5802c165ad46161f53555fb
https://doi.org/10.1002/9780471264194.fos03716.pub4
https://doi.org/10.1002/9780471264194.fos03716.pub4
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[15529-49-4] C54H45Cl2P3Ru (MW 958.86) InChI = 1/3C18H15P.2ClH.Ru/c3*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;/h3*1-15H;2*1H;/q;;;;;+2/p-2/f3C18H15P.2Cl.Ru/h;;;2*1h;/q;;;2*-1;m InChIKey = WIWBLJMBLGWSIN-ZAOJSHESCC (used in the hydrog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7661147f243dc1cd5cf5305f2d842c06
https://doi.org/10.1002/047084289x.rd137.pub3
https://doi.org/10.1002/047084289x.rd137.pub3
Autor:
F. H. Jardine
Publikováno v:
Progress in Inorganic Chemistry ISBN: 9780470166321
Progress in Inorganic Chemistry, Volume 31
Progress in Inorganic Chemistry, Volume 31
Preparation et reactions (substitution, oxydation, reduction, echange isotopique, isomerisation). Catalyseur d'hydrogenation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b358316c51a375c392d8ce8cf76ab828
https://doi.org/10.1002/9780470166321.ch4
https://doi.org/10.1002/9780470166321.ch4
Publikováno v:
Macromolecules. 28:1721-1723
Publikováno v:
IndraStra Global.
d -Fructose is hydrogenated to d -glucitol and d -mannitol using RuCl 2 (PPh 3 ) 3 as catalyst at 100°C and atmospheric pressure. Besides hydrogenation, fructose undergoes transfer hydrogenation when propan-2-ol and butan-2-ol are used as solvents.
Publikováno v:
ChemInform. 21
Autor:
Larry D. Markham, Brian R. James
Publikováno v:
Inorganic Chemistry. 13:97-100