| Literature DB >> 25767084 |
Paul Neumann1, Hanna Dib, Alix Sournia-Saquet, Toni Grell, Marcel Handke, Anne-Marie Caminade, Evamarie Hey-Hawkins.
Abstract
An efficient system for the catalytic redox isomerization of the allylic alcohol 1-octen-3-ol to 3-octanone is presented. The homogeneous ruthenium(II) catalyst contains a monodentate phosphane ligand with a ferrocene moiety in the backbone and provides 3-octanone in quantitative yields. The activity is increased by nearly 90 % with respect to the corresponding triphenyl phosphane ruthenium(II) complex. By grafting the catalyst at the surface of a dendrimer, the catalytic activity is further increased. By introducing different spacers between ferrocene and phosphorus, the influence on the electronic properties of the complexes is shown by evaluating the electrochemical behavior of the compounds.Entities:
Keywords: allylic alcohols; dendrimers; ferrocenes; homogeneous catalysis; phosphanes
Year: 2015 PMID: 25767084 DOI: 10.1002/chem.201406489
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236