Asymmetric synthesis of 3,5-dihydroxy-6(E)-heptenoate-containing HMG-CoA reductase inhibitors

This publication has 9 references indexed in Scilit:

• HMG‐CoA Reductase Inhibitors: An Exciting Development in the Treatment of Hyperlipoproteinemia
  Medicinal Research Reviews, 1991
• Stereoselective aldol reaction with chiral acetates
  Tetrahedron: Asymmetry, 1990
• A highly stereoselective route to the four stereoisomers of a six-carbon synthon
  Tetrahedron: Asymmetry, 1990
• A General Method for the Synthesis ofsyn-(E)-3,5-Dihydroxy-6-heptenoates
  Synlett, 1990
• Enantioselective synthesis of a new fluoro-substituted HMG-COA reductase inhibitor
  Tetrahedron Letters, 1989
• Directed reduction of .beta.-hydroxy ketones employing tetramethylammonium triacetoxyborohydride
  Journal of the American Chemical Society, 1988
• 1,3- diastereoselective reduction of β-hydroxyketones utilizing alkoxydialkylboranes
  Tetrahedron Letters, 1987
• Synthesis of an HMG-CoA reductase inhibitor; a diastereoselective aldol approach
  Tetrahedron Letters, 1987
• (R)- and (S)-2-acetoxy-1,1,2-triphenylethanol - effective synthetic equivalents of a chiral acetate enolate
  Tetrahedron Letters, 1984