Dissimilar behaviour of 3β, 16α‐dihydroxy‐5α‐androstan‐17‐one Diacetate under Basic and Acidic Conditions

This publication has 9 references indexed in Scilit:

• ¹³C NMR spectroscopic study of the rearrangement of 16β‐hydroxy‐17‐oxo steroids to 17β‐hydroxy‐16‐oxo isomers
  Magnetic Resonance in Chemistry, 1988
• Stereospecific 1,2-hydride shift in the rearrangement of 16.BETA.-hydroxy-17-oxo steroids to 17.BETA.-hydroxy-16-ones with acid and base.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1987
• Stereospecific synthesis of 16.alpha.-hydroxy-17-oxo steroids by controlled alkaline hydrolysis of corresponding 16-bromo-17-ketones and its reaction mechanism
  The Journal of Organic Chemistry, 1982
• Pyridine-induced solvent shifts in the nuclear magnetic resonance spectra of hydroxylic compounds
  Journal of the American Chemical Society, 1968
• Some Reactions of Steroidal α-Bromo Ketones¹
  The Journal of Organic Chemistry, 1966
• Die kernresonanzspektren von steroiden in polaren lösungsmitteln—II
  Tetrahedron, 1966
• Rearrangements of Steroidal Ring D Ketols¹
  Journal of the American Chemical Society, 1960
• The Action of Lead Tetraacetate on an Enol Acetate. The Epimeric 16-Acetoxy Derivatives of Epiandrosterone Acetate, their Interconversion and Rearrangement
  Journal of the American Chemical Society, 1957
• Studies of Steroid Ring D Epoxides of Enol Acetates; A New Synthesis of Estriol and of Androstane-3β,16α,17β-triol¹
  Journal of the American Chemical Society, 1954