Bouillon, J.-P.

Couve-Bonnaire, Samuel

Gaumont, A.-C.

Lakhdar, S.

Lalevée, J.

Lohier, J.-F.

Morlet-Savary, F.

Pannecoucke, Xavier

Rousée, Kevin

International audienceThis work describes the first transition metal-free stereospecific synthesis of (E)-(1-fluoro-2-arylvinyl)phosphine boranes through the addition of diarylphosphine-boranes to gem-bromofluoroalkenes in the presence of a base at room temperature. The reaction proceeds well under very mild conditions and tolerates a variety of functionalities. Scope and limitations of the reaction are discussed. Mechanistic investigations have been undertaken and revealed that the reaction takes place through an SRN1 mechanism. The formation of the fluorinated vinyl radical has been evidenced by electron paramagnetic resonance (EPR) experiment

HAL - Normandie Université

Transition metal-free stereospecific access to (E)-(1-fluoro-2-arylvinyl)phosphine borane complexes

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Transition metal-free stereospecific access to (E)-(1-fluoro-2-arylvinyl)phosphine borane complexes

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HAL - Normandie Université

Archive Ouverte en Sciences de l'Information et de la Communication