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

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

Detalles Bibliográficos
Main Authors: Davies, S, Fletcher, A, Roberts, P, Hughes, D
Formato: Journal article
Idioma:English
Publicado: 2010
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Títulos similares

  • Asymmetric synthesis of beta-amino-gamma-substituted-gamma-butyrolactones: double diastereoselective conjugate addition of homochiral lithium amides to homochiral alpha,beta-unsaturated esters.
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    Publicado: (2007)
  • The conjugate addition of enantiomerically pure lithium amides as homochiral ammonia equivalents: scope, limitations and synthetic applications
    por: Davies, S, et al.
    Publicado: (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: (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: (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: (2011)

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