Stereoselective approach to optically pure syn 2-amino alcohol derivatives

This publication has 22 references indexed in Scilit:

• Influence of stereochemistry on activity and binding modes for C2 symmetry-based diol inhibitors of HIV-1 protease
  Journal of the American Chemical Society, 1994
• Diastereoselective synthesis of the key lactone intermediate for the preparation of hydroxyethylene dipeptide isosteres
  Tetrahedron Letters, 1994
• Synthetic studies towards amino alcohols. Diastereocontrolled reduction of α′-chiral α,β-enones.
  Tetrahedron Letters, 1993
• Chiral synthons for 2-amino alcohols. Facile preparation of optically active amino hydroxy acids of biological interest.
  Tetrahedron, 1993
• Facile synthesis of potent HIV-1 protease inhibitors containing a novel pseudo-symmetric dipeptide isostere
  Journal of the Chemical Society, Chemical Communications, 1993
• A diastereoselective synthesis of pseudo-C2 -symmetric 1,3-diamino-2-propanols as core units in HIV protease inhibitors
  Tetrahedron, 1993
• α-Amino-β-hydroxy Acids in the Total Synthesis of Amino Sugars
  Synlett, 1993
• Stereoselective routes toward the synthesis of unusual amino acids
  Accounts of Chemical Research, 1992
• Inhibitors of HIV-1 Protease
  Journal of Enzyme Inhibition, 1992
• Asymmetric synthesis of α-amino acids from carbohydrates as chiral templates
  Tetrahedron, 1991