| Literature DB >> 16729338 |
Federica Zaccheria1, Nicoletta Ravasio, Rinaldo Psaro, Achille Fusi.
Abstract
A method for the anaerobic oxidation of a wide series of alcohols including cyclohexanols and steroidal alcohols, has been set up. It relies on a transfer dehydrogenation reaction from the substrate alcohol to styrene catalyzed by a heterogeneous, reusable copper catalyst under very mild liquid-phase experimental conditions (90 degrees C, N(2)) and shows unusual selectivity. Thus, the method is selective for the oxidation of secondary and allylic alcohols even in the presence of unprotected primary and benzylic alcohols. Electronic effects and the choice of the hydrogen acceptor account for the selectivity observed.Entities:
Year: 2006 PMID: 16729338 DOI: 10.1002/chem.200501619
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236