Synthetic Study on Antitumor Antibiotic Terpentecin: Construction of the Carbobicyclic Decalin Moiety

This publication has 16 references indexed in Scilit:

• Stereoselective Route to the Highly Oxidated Sidechain Moiety of Terpentecin and Related Antibiotics
  Chemistry Letters, 1996
• Alternation of stereocontrol mode in the cyclization of 2-(3′-4′-dimethyl-6′-trimethylsilyl-4′-hexenyl)-2-cyclohexenones by the auxiliary controlling substituents at 1′- and 2′-positions of the side chain
  Tetrahedron Letters, 1994
• Clerodane diterpenoids
  Natural Product Reports, 1992
• Topoisomerase-targeting antitumor drugs
  Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, 1989
• DNA TOPOISOMERASE POISONS AS ANTITUMOR DRUGS
  Annual Review of Biochemistry, 1989
• Total synthesis of the trans-clerodane diterpenoid (±)-stephalic acid
  Journal of the Chemical Society, Chemical Communications, 1989
• Isolation and characterization of terpentecin, a new antitumor antibiotic.
  The Journal of Antibiotics, 1985
• An efficient approach to chiral, nonracemic trans-decahydro-5,8a-dimethyl-1,6-naphthalenedione derivatives. Total synthesis of (+)-pallescensin A
  The Journal of Organic Chemistry, 1984
• The utility of silicon in organic synthesis
  Tetrahedron, 1983
• A Procedure for the Preparation of (S)-8a-Methyl-3,4,8,8a-tetrahydro-1,6(2H,7H)-naphthalenedione
  Synthesis, 1977