A general stereocontrolled approach to the 5-8 fused ring system. Application to the total synthesis of the marine natural product (.+-.)-precapnelladiene

This publication has 11 references indexed in Scilit:

• Reductive carbon-carbon cleavage in caged systems. A new general synthesis of linearly fused cis-syn-cis-triquinanes
  The Journal of Organic Chemistry, 1985
• General approach to annulated 4-cyclooctenones by aliphatic Claisen rearrangement. Stereospecific total synthesis of (.+-.)-precapnelladiene
  Journal of the American Chemical Society, 1985
• Synthesis of stereoisomeric 9a-methylhydrodicyclopenta[a,d]cyclooctan-1-ones related to the ophiobolins and ceroplastins via annelative ring expansion of hydrindene precursors
  The Journal of Organic Chemistry, 1985
• Capnellane sesquiterpenes. Total synthesis of epiprecapnelladiene and Δ⁸⁽⁹⁾-capnellene
  Journal of the Chemical Society, Perkin Transactions 1, 1982
• A novel, versatile synthetic approach to linearly fused tricyclopentanoids via photo-thermal olefin metathesis
  Tetrahedron, 1981
• Terpenoids—LXXVI
  Tetrahedron, 1979
• Poitediol, a new nonisoprenoid sesquiterpene diol from the marine alga Laurencia poitei
  The Journal of Organic Chemistry, 1978
• Marine natural products: dactylol, a new sesquiterpene alcohol from a sea hare
  Tetrahedron, 1978
• A synthesis of the ophiobolin nucleus
  The Journal of Organic Chemistry, 1977
• Terpenoids—LXXII11For part LXXI, see Y.M. Sheikh, G. Singy, M. Kaisin, H. Eggert, C. Djerassi, B. Tursch, D. Daloze and J.C. Braekman, Tetrahedron 32, 1171 (1976).
  Tetrahedron, 1977