P-Chirogenic Binaphthyl-Substituted Monophosphines: Synthesis and Use in Enolate Vinylation/Arylation Reactions

Abstract
New phosphine ligands possessing both axial chirality and a chirogenic phosphorus center were prepared from (R)-2-bromo-2‘-N,N-(dimethylamino)-1,1‘-binaphthyl (1) via a simple Li−halogen exchange protocol. The asymmetric vinylation of a ketone enolate with (R,RP)-2-(tert-butylphenylphosphino)-2‘-N,N-(dimethylamino)-1,1‘-binaphthyl (2a) afforded the coupling product with good enantiomeric excess.

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