Exhaustively substituted bile acids as chiral selectors for enantioselective chromatography

This publication has 13 references indexed in Scilit:

• Synthesis of four cholic acid-based CSPs containing 2-naphthoyl carbamate and 3,5-dinitrophenylcarbamate moieties and their evaluation in the HPLC resolution of racemic compounds
  Tetrahedron: Asymmetry, 2002
• Highly Diastereoselective Synthesis of the 1,1‘-Binaphthol Unit on a Bile Acid Template
  The Journal of Organic Chemistry, 2000
• Bile Acid-Derived Molecular Tweezers: Study of Solvent Effects in Binding, and Determination of Thermodynamic Parameters by an Extraction-Based Protocol
  The Journal of Organic Chemistry, 2000
• Synthesis of a new family of four deoxycholic acid derived chiral stationary phases and their evaluation in the HPLC resolution of racemic compounds
  Tetrahedron: Asymmetry, 1999
• Steroidal guanidinium receptors for the enantioselective recognition of N-acyl α-amino acids
  Chemical Communications, 1999
• Bile acids as stationary phase in liquid chromatography
  Chromatographia, 1998
• Synthesis, characterization and enantioselectivity of cholic acid-bonded phases for high performance liquid chromatography
  Chromatographia, 1997
• Design, Synthesis, and Evaluation of Bile Acid-Based Molecular Tweezers
  The Journal of Organic Chemistry, 1996
• Cholaphanes et al.; steroids as structural components in molecular engineering
  Chemical Society Reviews, 1993
• Considerations of chiral recognition relevant to the liquid chromatography separation of enantiomers
  Chemical Reviews, 1989