Stereoselective Palladium-Catalyzed C–F Bond Alkenylation of Tetrasubstituted <i>gem</i>-Difluoroalkenes via Mizoroki–Heck Reaction
Yanhui Wang, Gavin Chit Tsui
Abstract
High Resolution Image Download MS PowerPoint Slide A highly diastereoselective Pd(0)-catalyzed Mizoroki–Heck reaction of gem -difluoroalkenes is described. Unlike previously reported C–F bond functionalization with organometallic reagents, this reaction takes place between two different alkenes to achieve a formal C–F and C–H bond cross-coupling via a distinct pathway. Monofluorinated 1,3-diene products can be synthesized with control of the geometry of each alkene and good functional group tolerability.
Topics & Concepts
ChemistryAlkenePalladiumCatalysisReagentCombinatorial chemistryStereoselectivityFunctional groupMedicinal chemistryOrganic chemistryPolymerFluorine in Organic ChemistryCatalytic Cross-Coupling ReactionsCatalytic C–H Functionalization Methods