| Literature DB >> 32013430 |
Sota Akiyama1, Syogo Nomura1, Koji Kubota1,2, Hajime Ito1,2.
Abstract
A method to synthesize 3-boryl-1,1-gem-difluorodienes via the copper(I)-catalyzed boryl substitution of trifluoromethyl-substituted allenes was developed. The borylated compounds were obtained up to 91% yield with excellent selectivity. We proposed that the reaction proceeded via γ-selective borylcupration into the trifluoromethyl-substituted allene, followed by copper(I)-β-fluoro elimination. Subsequent transformations of the borylation product by Suzuki-Miyaura cross-coupling or Diels-Alder reaction provided various compounds bearing a difluoro moiety, which are difficult to synthesize by existing methods.Entities:
Year: 2020 PMID: 32013430 DOI: 10.1021/acs.joc.9b03353
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354