Asymmetric syntheses of enantiopure C(5)-substituted transpentacins via diastereoselective Ireland-Claisen rearrangements.

Slični predmeti

• Diastereoselective Ireland-Claisen rearrangements of substituted allyl β-amino esters: applications in the asymmetric synthesis of C(5)-substituted transpentacins.
  od: Davies, S, i dr.
  Izdano: (2014)
• Doubly diastereoselective [3,3]-sigmatropic aza-Claisen rearrangements.
  od: Davies, S, i dr.
  Izdano: (2009)
• Double diastereoselective [3,3]-sigmatropic aza-Claisen rearrangements.
  od: Davies, S, i dr.
  Izdano: (2003)
• Double asymmetric induction as a mechanistic probe: the doubly diastereoselective conjugate addition of enantiopure lithium amides to enantiopure alpha,beta-unsaturated esters and enantiopure alpha,beta-unsaturated hydroxamates
  od: Davies, S, i dr.
  Izdano: (2011)
• Double asymmetric induction as a mechanistic probe: the doubly diastereoselective conjugate addition of enantiopure lithium amides to enantiopure alpha,beta-unsaturated esters and enantiopure alpha,beta-unsaturated hydroxamates
  od: Davies, S, i dr.
  Izdano: (2011)