130 research outputs found
CD80 down-regulation is associated to aberrant DNA methylation in non-inflammatory colon carcinogenesis
Metal-catalysed synthesis of nitroenaminones from α-nitroketones or -esters and nitriles
ChemInform Abstract: Solution Dynamics of the Reversible Carbonyl-Phosphorus Ligand Exchange in (OC)<sub>4</sub>Mo(μ-PEt<sub>2</sub>)<sub>2</sub>Mo(CO)<sub>4</sub>: Kinetic Parameters as a Measure of the Relative Steric Hindrance of Phosphines and Phosphites.
Carbon−carbon bond formation upon addition of cyanogen to metal-coordinated β-carbonylenolato and β-ketoiminato ligands
Carboncarbon bond formation upon addition of cyanogen to metal-coordinated β-carbonylenolato and β-ketoiminato ligands
ChemInform Abstract: REDOX-RK.-MECHANISMEN IN NICHT-KOMPLEMENTAEREN PROZESSEN 2. MITT. KINETIK DER UMWANDLUNGEN PLATIN(II)-EISEN(III) UND EISEN(II)-PLATIN(IV)
Nichel (0) complexes with the hybrid bidentate ligand 1-(thioethyl)-2-(diphenylphosphino)ethane. Syntesis and catalytic properties of the related nickel hydride derivative
Reductive carbonylation of Phosphino-complexes of cobalt(II), a kinetic investigation
The stoichiometry and kinetics of the reaction of carbon monoxide with [CoI2(CO)(PEt3)2] were examined in different solvents and in the presence of free PEt3. The results are interpreted in terms of a mechanism in which an iodide-bridged dicobalt species undergoes carbon monoxide addition to give an intermediate which is reduced by external PEt3. © 1982
Reductive Carbonylation of Phosphine-Complexes of Cobalt(II). A Kinetic Investigation
The stoichiometry and kinetics of the reaction of carbon monoxide with [CoI2(CO)(PEt3)2] were examined in different solvents and in the presence of free PEt3. The results are interpreted in terms of a mechanism in which an iodide-bridged dicobalt species undergoes carbon monoxide addition to give an intermediate which is reduced by external PEt3. © 1982
Solventless silane alcoholysis catalyzed by recoverable dirhodium(II) perfluorocarboxylates
We have developed a novel reaction protocol for the highly efficient and sustainable catalysis of the silane alcoholysis reaction. The catalysts of choice are dirhodium(II) perfluorocarboxylates bearing long perfluoroalkyl chains, which are easily prepared in one step from commercial precursors. Under optimized reaction conditions, these catalysts exhibit up to about 50 times higher activity and 100 times higher productivity than analogous dirhodium(II) complexes described in the prior art. Furthermore, the reaction can be run in a completely solventless fashion. Finally, heterogenization of these catalysts has been accomplished through a novel strategy based on fluorous chemistry. Indeed, perfluorinated catalysts of this kind are easily adsorbed on silica which has been previously functionalized at its surface with perfluoroalkyl chains. Use of such supported catalysts (bonded fluorous phase catalysts) allows an easy and almost complete catalyst separation and recycling with improved catalytic performance
- …
