BIFUNCTIONAL CHIRAL AUXILIARIES .6. ALKYLATIONS OF ENOLATES DERIVED FROM 1,3-DIACYLIMIDAZOLIDINE-2-THIONES AMD 1,3-DIACYLIMIDAZOLIDIN-2-ONES

Sodium and potassium enolates of 1,3-diacylimidazolidin-2-ones undergo clean alkylation reactions with reactive alkyl halides; the latter en olates reacting generally more stereoselectively due, it is proposed, to the lower temperature at which the reactions proceed. The reactions are all stereoregular, with the diastereoisomeric identity of product s being established unambiguously by the synthesis of (2S)-3-phenyl-2- methylpropan-1-ol. The sense of asymmetric induction in these reaction s is consistent with the intermediacy of chelated syn enolates which t he electrophile approaches preferentially from the face exo to the pro ximate alkyl / aryl group on the five-membered ring. In contrast, 1,3- diacylimidazolidine-2-thiones are unable to act as bifunctional chiral auxiliaries in alkylation reactions due to enolate decomposition.