Utilization of the chiral synthon, methyl 3-O-benzyl-2,4,6-trideoxy-6-iodo-α-D-erythro-hexopyranoside in the synthesis of a potent HMG-CoA reductase inhibitor

This publication has 9 references indexed in Scilit:

• A novel diastereoselective synthesis of the lactone moiety of compactin
  Tetrahedron Letters, 1984
• Synthetic and biological studies of compactin and related compounds. 2. Synthesis of the lactone moiety of compactin
  The Journal of Organic Chemistry, 1984
• Total synthesis of (+)-dihydrocompactin
  Journal of the American Chemical Society, 1984
• Synthesis of 2,4-dideoxy-d-erythro-hexopyranose. An intermediate for synthesis of the lactone moiety of inhibitors of hydroxymethylglutaryl-coenzyme A reductase
  Carbohydrate Research, 1984
• Mevinic acids and analogues: preparation of a key chiral intermediate
  Tetrahedron Letters, 1982
• Methyl 3-0-benzyl-2,4,6-trideoxy-6-iodo-α-d-erythro-hexopyranoside, a chiral synthon for the synthesis of inhibitors of HMG-CoA reductase
  Tetrahedron Letters, 1982
• Oxidation of Alcohols withN-Halosuccinimides-New and Efficient Variants
  Synthesis, 1981
• Alkylative eliminations. Scope of the activating group
  The Journal of Organic Chemistry, 1975
• Ein neues Verfahren zur Herstellung von 21‐Desoxy‐aldosteron und 21‐Desoxy‐17‐iso‐aldosteron. Über Steroide, 203. Mitteilung
  Helvetica Chimica Acta, 1963