| Literature DB >> 22308217 |
Scott P Simonovich1, Jeffrey F Van Humbeck, David W C Macmillan.
Abstract
A new enantioselective α-oxidation of aldehydes has been accomplished using TEMPO and a synergistic combination of copper and organic catalysis. Expanding upon recently reported mechanistic studies, these mild catalytic conditions provide stable aldehyde products bearing a wide array of electronically and sterically diverse substructures. The utility of these oxidized products is highlighted by subsequent derivatization to a variety of common chiral synthons, without loss in enantiopurity.Entities:
Year: 2012 PMID: 22308217 PMCID: PMC3269783 DOI: 10.1039/c1sc00556a
Source DB: PubMed Journal: Chem Sci ISSN: 2041-6520 Impact factor: 9.825