Synthetic studies of trichothecenes, an enantioselective synthesis of a C-ring precursor of anguidine

This publication has 18 references indexed in Scilit:

• Synthesis of a bicyclic precursor to verrucarol: application of a trimethylsilyl-controlled Diels-Alder reaction and Wagner-Meerwein rearrangement sequence
  The Journal of Organic Chemistry, 1981
• Organoiron complexes in organic synthesis. Part 19. Trichothecene analogs. Total synthesis of 12,13-epoxy-14-methoxytrichothecene via organoiron complexes
  Journal of the American Chemical Society, 1981
• Novel synthesis of the tricyclic nucleus of verrucarol
  The Journal of Organic Chemistry, 1981
• Synthetic studies toward verrucarol. 2. Synthesis of the AB ring system
  The Journal of Organic Chemistry, 1980
• Synthetic studies toward verrucarol. 1. Synthesis of the AB ring system
  The Journal of Organic Chemistry, 1980
• Stereoselective total synthesis of (.+-.)-trichodiene: biogenetic precursor of the trichothecane sesquiterpenoids
  The Journal of Organic Chemistry, 1980
• Total synthesis of verrucarol: a stereoselective synthesis of 13,14-dinor-15-hydroxytrichothec-9-ene
  The Journal of Organic Chemistry, 1980
• Synthetic studies on the sesquiterpene antibiotic verrucarol
  Journal of the Chemical Society, Perkin Transactions 1, 1978
• A synthesis of 12,13-epoxytrichothec-9-ene
  Tetrahedron Letters, 1976
• Total synthesis of (±)-12,13-epoxytrichothec-9-ene.
  Tetrahedron Letters, 1974