168298-09-7Relevant articles and documents
4-Substituted-5,5-Dimethyl Oxazolidin-2-ones as Effective Chiral Auxiliaries for Enolate Alkylations and Michael Additions
Davies, Stephen G.,Sanganee, Hitesh J.
, p. 671 - 674 (1995)
4-(Methyl, phenyl, benzyl, and i-propyl)-5,5-dimethyl-oxazolidin-2-ones, readily available from α-amino acids, are shown to be effective chiral auxiliaries for stereoselective enolate alkylations and conjugate additions of attached N-acyl moieties.
The 'SuperQuat' (R)-4-phenyl-5,5-dimethyl oxazolidin-2-one as an effective chiral auxiliary for conjugate additions: Asymmetric synthesis of (-)-aplysillamide B.
Davies, Stephen G.,Sanganee, Hitesh J.,Szolcsanyi, Peter
, p. 3337 - 3354 (2007/10/03)
(R)-4-Phenyl-5,5-dimethyl-oxazolidin-2-one, readily available from D- phenylglycine, is shown to be an effective chiral auxiliary for stereoselective conjugate additions to attached α,β-unsaturated N-acyl moieties. Its utility is demonstrated by the asymmetric synthesis of the antifungal, antibacterial (-)-Aplysillamide B.