Sökning: "metal carbonyl"
Visar resultat 1 - 5 av 40 avhandlingar innehållade orden metal carbonyl.
1. Transition Metal-Mediated Selective Functionalizations of Bio-Derived Building Blocks
Sammanfattning : In order to transition to a more sustainable chemical industry, it is necessary to replace the fossil starting materials that are largely used today with renewable ones. Starting materials available from abundant natural sources, or which can be efficiently produced via a biotransformation, are of high interest in this regard. LÄS MER
2. Transition metal-catalyzed reduction of carbonyl compounds : Fe, Ru and Rh complexes as powerful hydride mediators
Sammanfattning : A detailed mechanistic investigation of the previously reported ruthenium pseudo-dipeptide-catalyzed asymmetric transfer hydrogenation (ATH) of aromatic ketones was performed. It was found that the addition of alkali metals has a large influence on both the reaction rate and the selectivity, and that the rate of the reaction was substantially increased when THF was used as a co-solvent. LÄS MER
3. Transition metal-catalysed isomerisation of allylic alcohols : Applications to C−C, C−F and C−Cl bond formation
Sammanfattning : The focus of this thesis has been to develop selective and atom-economical methods for carbon-carbon and carbon-heteroatom bond formation, and to some extent improve on existing findings in this area. More specifically, methods for the catalytic generation of enolates from allylic alcohols and their in situ functionalisation with electrophilic reagents are described. LÄS MER
4. Copper(I) Alkoxides and Aryloxides
Sammanfattning : Copper(I) alkoxides and aryloxides have been prepared from mesitylcopper(I) and alcohols or phenols. The solid state structures of the alkoxides and aryloxides are .my.2- and/or . LÄS MER
5. Fundamental interactions in transition metal reactions
Sammanfattning : Transition metal complexes that participate in homogeneous reactions often perform the role of a catalyst, facilitating novel reaction pathways. When these complexes are pushed away from their equilibrium, the arrangement of the coordinating ligands around the metal center is perturbed and new reaction pathways are opened. LÄS MER