A 2,3-butanedione protected chiral glycine equivalent--a new building block for the stereoselective synthesis of enantiopure N-protected alpha-amino acids.

Slični predmeti

• A 2,3-butanedione protected chiral glycine equivalent - A new building block for the stereoselective synthesis of enantiopure N-protected α-amino acids
  od: Dixon, D, i dr.
  Izdano: (2003)
• The preparation and alkylation of a butanedione-derived chiral glycine equivalent and its use for the synthesis of alpha-amino acids and alpha,alpha-disubstituted amino acids
  od: Harding, C, i dr.
  Izdano: (2004)
• 6-methyl delta-lactol derived chiral glycine equivalents for the asymmetric synthesis of protected alpha-amino amides
  od: Dixon, D, i dr.
  Izdano: (2004)
• Butane-2,3-diacetal-desymmetrized glycolic acid—a new building block for the stereoselective synthesis of enantiopure α-hydroxy acids
  od: Díez, E, i dr.
  Izdano: (2001)
• A stereoselective oxy-Michael route to protected beta-aryl-beta-hydroxy-alpha-amino acids
  od: Hernandez-Juan, F, i dr.
  Izdano: (2006)