| Literature DB >> 28646533 |
Hai-Jun Tang1, Ling-Zhi Lin1, Chao Feng1, Teck-Peng Loh2.
Abstract
A Pd-catalyzed fluoroarylation of gem-difluoroalkenes with aryl halides is reported. By taking advantage of the in situ generated α-CF3 -benzylsilver intermediates derived from the nucleophilic addition of silver fluoride to gem-difluoroalkenes, this strategy bypasses the use of a strong base, thus enabling a mild and general synthetic method for ready access to non-symmetric α,α-disubstituted trifluoroethane derivatives.Entities:
Keywords: arylation; cross-coupling; fluorination; gem-difluoroalkenes; palladium
Year: 2017 PMID: 28646533 DOI: 10.1002/anie.201705321
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336