| Literature DB >> 12688795 |
Giovanni Sartori1, Alan Armstrong, Raimondo Maggi, Alessandro Mazzacani, Raffaella Sartorio, Franca Bigi, Belen Dominguez-Fernandez.
Abstract
The dioxirane-mediated epoxidation of alkenes in the presence of supported alpha-fluorotropinones 5 and 9 has been evaluated. The catalysts anchored onto silica supports 5 have shown comparable activity with respect to the homogeneous counterpart 10 and good stability on recycling. In the second part of this paper the enantiomerically enriched alpha-fluorotropinone 4 was anchored onto both mesoporous MCM-41 and amorphous KG-60 silicas. The chiral-supported catalysts promoted the stereoselective epoxidation of several trans-substituted and trisubstituted alkenes with ee values up to 80% and were perfectly reusable with the same performance for at least three catalytic cycles.Entities:
Year: 2003 PMID: 12688795 DOI: 10.1021/jo034044c
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354