| Literature DB >> 32523163 |
Suvajit Koley1, Ryan A Altman1.
Abstract
gem-Difluorinated alkenes are readily accessible building blocks that can undergo functionalization to provide a broad spectrum of fluorinated and non-fluorinated products. Herein, we review recent (since 2017) transition metal-catalyzed transformations of these specialized alkenes and summarize general reactivity patterns of these reactions. Many transition metal-catalyzed reactions undergo net C-F bond functionalization reactions to deliver monofluorinated products. These reactions typically proceed through β-fluoro alkylmetal intermediates that readily eliminate a β-fluoride to deliver monofluoroalkene products. A second series of reactions exploit coinage metal fluorides to add F- to the gem-difluorinated alkene, and further functionalization delivers trifluoromethyl-containing products. In stark contrast, few transition metal-catalyzed reactions proceed in net "fluorine-retentive processes" to deliver difluoromethylene-based products.Entities:
Keywords: C–F functionalization; fluorination; gem-difluoroalkenes; transition metal catalysts; β-fluoride elimination
Year: 2020 PMID: 32523163 PMCID: PMC7286626 DOI: 10.1002/ijch.201900173
Source DB: PubMed Journal: Isr J Chem ISSN: 0021-2148 Impact factor: 3.333