Bile acids. OV. 2,2-Dimethoxypropane: an esterifying agent preferred to diazomethane for chenodeoxycholic acid.

This publication has 16 references indexed in Scilit:

• Intramolecular catalysis. VIII. Effects on the acetylation of the 7.alpha.-hydroxyl group of steroids. Proton nuclear magnetic resonance rate method
  The Journal of Organic Chemistry, 1975
• PURITY CRITERIA FOR CHENODEOXYCHOLIC ACID
  The Lancet, 1974
• NATURE OF CRYSTALLINE CHENODEOXYCHOLIC ACID
  The Lancet, 1974
• The methylation of some phenols and alcohols with sodium hydride / methyl iodide in tetrahydrofuran at room temperature
  Tetrahedron Letters, 1973
• Improved Aldehyde Synthesis: Preparation of 3?, 7?, 12?-Triacetoxy-5?-Cholan-23-al with Ruthenium Tetroxide in Neutral Medium
  Synthetic Communications, 1973
• Specificity of trimethylsilanol elimination in the mass spectra of the trimethylsilyl derivatives of di- and tri-hydroxy-steroids
  Journal of the Chemical Society, Chemical Communications, 1972
• Quantitative estimation of bile salts in serum
  Canadian Journal of Biochemistry, 1970
• Steroids. CCCX. Structure-activity relation of some steroidal hypnotic agents
  Journal of Medicinal Chemistry, 1968
• Aluminiumchlorid-katalysierte Verätherung von Alkoholen mit Diazoalkanen, III
  European Journal of Organic Chemistry, 1964
• Verätherung von Alkoholen mit Diazomethan unter Borfluorid‐Katalyse
  Angewandte Chemie, 1958