Stereoselective total synthesis of β-2,7,11-Cembratriene-4,6-diol (β-CBT), a tumor inhibitory constituent of tobacco smoke

This publication has 11 references indexed in Scilit:

• Stereoselective synthesis of cembranolides via conjugate addition to cycloalkynones
  Tetrahedron Letters, 1987
• Synthesis of cembrane natural products via [2,3] Wittig ring contraction of propargylic ethers
  The Journal of Organic Chemistry, 1987
• Identification of cembratriene-4,6-diol as antitumor-promoting agent from cigarette smoke condensate
  Carcinogenesis: Integrative Cancer Research, 1985
• Oxidation of alcohols by “activated” dimethyl sulfoxide. a preparative, steric and mechanistic study
  Tetrahedron, 1978
• CYCLIZATION OF POLYENES XXII. SYNTHESIS AND STEREOCHEMISTRY OF THUNBERGOL
  Chemistry Letters, 1977
• The stereoselective total synthesis of pseudoguaianolides: confertin
  Journal of the American Chemical Society, 1976
• The structure of a new type of plant growth inhibitor extracted from immature tobacco leaves
  Tetrahedron Letters, 1975
• The Synthesis and Stereochemistry of Isomeric 16-Hydroxy-17(20)-pregnenes
  The Journal of Organic Chemistry, 1964
• Macrocyclic Diterpenes. α- and β-4,8,13-Duvatriene-1,3-diols from Tobacco¹
  The Journal of Organic Chemistry, 1962
• Communications- Hydrazine Reduction of α, β-Epoxy Ketones to Allylic Alcohols
  The Journal of Organic Chemistry, 1961