| Literature DB >> 26727513 |
Takeshi Fujita1, Kazuki Sugiyama1, Shohei Sanada1, Tomohiro Ichitsuka1, Junji Ichikawa1.
Abstract
The synthesis of difluoromethylene-containing heterocycles was achieved via the palladium-catalyzed 1,1-difluoroallylation of heteronucleophiles followed by intramolecular Heck reaction. The allylic substitution of 3-bromo-3,3-difluoropropene was regioselectively accomplished by heteronucleophiles without rearrangement to give the corresponding 1,1-difluoroallylated compounds whose Heck cyclization proceeded in a 5-exo manner to afford ring-difluorinated indolines and dihydrobenzofurans. Their defluorinative allylic substitution further provided 2-fluoroindoles and 2-fluorobenzofurans.Entities:
Year: 2016 PMID: 26727513 DOI: 10.1021/acs.orglett.5b03390
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005