| Literature DB >> 29645324 |
Clare Bakewell1, Andrew J P White1, Mark R Crimmin1.
Abstract
A series of industrially relevant fluoroalkenes react with a monomeric AlI complex. These reactions break strong sp2 and sp3 C-F bonds, and result in the formation of a diverse array of organoaluminium compounds. Mechanistic studies show that two mechanisms are likely in operation: 1) direct oxidative addition of the C-F bond to AlI occurs with retention of alkene stereochemistry, and 2) stepwise formation and decomposition of a metallocyclopropane intermediate occurs with inversion of alkene stereochemistry. As part of this mechanistic analysis, we have isolated the first aluminium metallocyclopropane complex from oxidative addition of an alkene to AlI . Remarkably this reaction is reversible and reductive elimination of the alkene occurs at higher temperature reforming AlI . Furthermore, in selected cases the organoaluminium products are susceptible toward β-fluoride elimination to yield a double C-F activation pathway.Entities:
Keywords: HFOs; aluminum; fluoride elimination; fluoroolefins; hydrofluorocarbons
Year: 2018 PMID: 29645324 DOI: 10.1002/anie.201802321
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336