| Literature DB >> 12003563 |
Scott E Denmark1, Hayao Matsuhashi.
Abstract
Two structurally dissimilar, chiral fluoro ketones have been prepared and their potential as enantioselective catalysts for asymmetric epoxidation with Oxone has been evaluated. The tropinone-based ketone (-)-5 was easily prepared and showed excellent reactivity but only modest enantioselectivity. The biphenyl-based ketone (-)-6 was prepared in a somewhat lengthy synthesis (along with its monofluoro and geminal fluoro analogues). This ketone exhibited only modest reactivity; 30 mol % of (-)-6 was needed to bring about complete conversion in a reasonable time. The enantioselectivity of this catalyst was generally much higher, but again very substrate dependent.Entities:
Year: 2002 PMID: 12003563 DOI: 10.1021/jo020050h
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354