Transition metal-free and regioselective vinylation of phosphine oxides and <i>H</i>-phosphinates with VBX reagents
Laura Castoldi, Adam A. Rajkiewicz, Berit Olofsson
Abstract
A series of phosphine oxides and H-phosphinates were vinylated in the presence of the iodine(iii) reagents vinylbenziodoxolones (VBX), providing the corresponding alk-1-enyl phosphine oxides and alk-1-enyl phosphinates in good yields with complete chemo- and regioselectivity. The vinylation proceeds in open flask under mild and transition metal-free conditions.
Topics & Concepts
RegioselectivityPhosphineReagentChemistryTransition metalIodineMetalOrganic chemistryCatalysisFluorine in Organic ChemistryAsymmetric Synthesis and CatalysisOxidative Organic Chemistry Reactions