AN IMPROVED ASYMMETRIC SYNTHESIS OF (R)-(−)-2-ACETYL-5,8-DIMETHOXY-1,2,3,4-TETRAHYDRO-2-NAPHTHOL. A VERSATILE KEY SYNTHETIC INTERMEDIATE OF OPTICALLY ACTIVE ANTHRACYCLINONES

This publication has 8 references indexed in Scilit:

• Unprecedented regio- and stereochemical control in the addition of organoaluminum reagents to chiral .alpha.,.beta.-unsaturated acetals
  Journal of the American Chemical Society, 1984
• Novel synthesis of optically pure anthracyclinone intermediates by the use of microbial asymmetric reduction with fermenting baker's yeast.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1984
• Novel resolution of the anthracyclinone intermediate by the use of (2r, 3r)-(+)- and (2s, 3s)-(-).1,4-bis(4-chlorobenzyloxy)butane-2,3-diol
  Tetrahedron, 1984
• CHIRAL MEDIA FOR ASYMMETRIC SOLVENT INDUCTIONS. (S,S)-( + )-1,4-BIS(DIMETHYLAMINO)-2,3-DIMETHOXYBUTANE FROM (R,R)-( + )-DIETHYL TARTRATE
  Organic Syntheses, 1983
• Asymmetric synthesis of optically active anthracyclinone intermediate and 4-demethoxyanthracyclinones by the use of a novel chiral reducing agent.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1983
• Development of a novel synthetic route to optically active anthracyclinones: Preliminary synthesis of the racemic key intermediate.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1983
• A high yield synthesis of (±)-5,8-dimethoxy-2-α-hydroxyethyl-3,4-dihydronaphthalene, a key intermediate in anthracyclinone synthesis
  Tetrahedron Letters, 1981
• Asymmetric halolactonization reactions. 3. Asymmetric synthesis of optically active anthracyclinones.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1979