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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

Xehetasun bibliografikoak
Egile Nagusiak: Davies, S, Fletcher, A, Roberts, P, Hughes, D
Formatua: Journal article
Hizkuntza:English
Argitaratua: 2010
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Antzeko izenburuak

  • Asymmetric synthesis of beta-amino-gamma-substituted-gamma-butyrolactones: double diastereoselective conjugate addition of homochiral lithium amides to homochiral alpha,beta-unsaturated esters.
    nork: Cailleau, T, et al.
    Argitaratua: (2007)
  • The conjugate addition of enantiomerically pure lithium amides as homochiral ammonia equivalents: scope, limitations and synthetic applications
    nork: Davies, S, et al.
    Argitaratua: (2005)
  • Doubly diastereoselective conjugate addition of homochiral lithium amides to homochiral alpha,beta-unsaturated esters containing cis- and trans-dioxolane units.
    nork: Davies, S, et al.
    Argitaratua: (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
    nork: Davies, S, et al.
    Argitaratua: (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
    nork: Davies, S, et al.
    Argitaratua: (2011)

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