Vitamin D C-22 aldehydes. New key intermediates for the synthesis of side chain modified vitamin D analogues

This publication has 14 references indexed in Scilit:

• Synthesis of 25-hydroxy- and 1.alpha.,25-dihydroxy vitamin D3 from vitamin D2 (calciferol)
  The Journal of Organic Chemistry, 1986
• Synthesis of 1α,25-dihydroxyvitamin D2, its 24 epimer and related isomers, and their binding affinity for the 1,25-dihydroxyvitamin D3 receptor
  Bioorganic Chemistry, 1985
• Synthesis of 1.ALPHA.,25-dihydroxy-26,27-dimethylvitamin D3, a highly active analogue of 1.ALPHA.,25-dihydroxyvitamin D3.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1985
• Synthesis and biological activity of 1.ALPHA.-hydroxy-24,24-dimethyl-22E-dehydrovitamin D3 and 1.ALPHA.,25-dihydroxy-24,24-dimethyl-22E-dehydrovitamin D3.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1984
• Synthesis of 25-hydroxyvitamin D2 and its 24-epimer
  The Journal of Organic Chemistry, 1984
• Synthesis and biological activity of (22E,24R)- and (22E,24S)-1.ALPHA.,24-dihydroxy-22-dehydrovitamin D3.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1984
• Facile and stereoselective synthesis of 25-hydroxyvitamin d2
  Tetrahedron Letters, 1984
• Synthesis of 23,23-difluoro-25-hydroxyvitamin D3
  Tetrahedron Letters, 1984
• Studies on the synthesis of side chain hydroxylated metabolites of vitamin D. Stereospecific syntheses of 25-hydroxy-7,8-dihydroergosterol and its C-24 epimer
  Tetrahedron Letters, 1983
• Synthesis of calcitroic acid, a metabolite of 1.alpha.,25-dihydroxycholecalciferol
  The Journal of Organic Chemistry, 1981