Lithium amides as homochiral ammonia equivalents for conjugate additions to α β-unsaturated esters: Asymmetric synthesis of (S)-β-leucine

Registos relacionados

• Asymmetric synthesis of beta-amino-gamma-substituted-gamma-butyrolactones: double diastereoselective conjugate addition of homochiral lithium amides to homochiral alpha,beta-unsaturated esters.
  Por: Cailleau, T, et al.
  Publicado em: (2007)
• The conjugate addition of enantiomerically pure lithium amides as homochiral ammonia equivalents: scope, limitations and synthetic applications
  Por: Davies, S, et al.
  Publicado em: (2005)
• Doubly diastereoselective conjugate addition of homochiral lithium amides to homochiral alpha,beta-unsaturated esters containing cis- and trans-dioxolane units.
  Por: Davies, S, et al.
  Publicado em: (2009)
• ASYMMETRIC-SYNTHESIS OF R-BETA-AMINO BUTANOIC ACID AND S-BETA-TYROSINE - HOMOCHIRAL LITHIUM AMIDE EQUIVALENTS FOR MICHAEL ADDITIONS TO ALPHA,BETA-UNSATURATED ESTERS
  Por: Davies, S, et al.
  Publicado em: (1991)
• Double asymmetric induction as a mechanistic probe: the doubly diastereoselective conjugate addition of enantiopure lithium amides to enantiopure α,β-unsaturated esters and enantiopure α,β-unsaturated hydroxamates
  Por: Davies, S, et al.
  Publicado em: (2011)