Synthesis of a Family of Fine-Tunable New Chiral Ligands for Catalytic Asymmetric Synthesis. Ligand Optimization through the Enantioselective Addition of Diethylzinc to Aldehydes

This publication has 34 references indexed in Scilit:

• A Straightforward, Highly Stereoselective Synthesis of Protected Isostatine Derivatives
  Chemistry – A European Journal, 1996
• Ready access to stereodefined β-hydroxy-γ-amino acids. Enantioselective synthesis of fully protected cyclohexylstatine
  Tetrahedron, 1996
• Enantioselective synthesis of fully protected anti 3-amino-2-hydroxy butyrates
  Tetrahedron: Asymmetry, 1995
• A convenient, stereodivergent approach to the enantioselective synthesis of N-Boc-aminoalkyl epoxides
  Tetrahedron Letters, 1995
• A concise enantioselective synthesis of allylamines and N-boc-β-amino acids
  Tetrahedron Letters, 1994
• A short enantioselective synthesis of N-Boc-α-amino acids from epoxy alcohols
  Tetrahedron Letters, 1993
• The chiral pool as a source of enantioselective catalysts and auxiliaries
  Chemical Reviews, 1992
• A versatile enantiospecific approach to 3-azetidinols and aziridines
  Tetrahedron Letters, 1991
• Regioselective ring opening of chiral epoxyalcohols by primary amines
  Tetrahedron Letters, 1991
• Mechanism of the gas-phase thermolysis of monomethylsilane
  Journal of the American Chemical Society, 1987