Synthetic study of ciguatoxin. Absolute configuration of the C2 hydroxy group

This publication has 37 references indexed in Scilit:

• syn-trans Fused Bicyclic Ether Formation via Acetylene-biscobalthexacarbonyl Complex
  Chemistry Letters, 1996
• Partial Synthesis of Ciguatoxin, an A/B/C Fragment
  Synlett, 1996
• Enantio-Controlled Synthesis of the AB Ring Moiety of Ciguatoxin
  Synlett, 1995
• Synthesis of two Diastereoisomers of A/B Fragment of Ciguatoxin
  Synlett, 1995
• Construction of the C46-C55 Fragment of Ciguatoxin
  Chemistry Letters, 1994
• Total Synthesis of (+)-Carbonolide B
  The Journal of Organic Chemistry, 1994
• Simple Designs for the Construction of Complex trans-Fused Polyether Toxin Frameworks. A Linear Strategy Based on Entropically Favored Oxirane Ring Enlargement in Epoxycycloalkenes Followed by Carbon-Carbon or Carbon-Oxygen Bond-Forming Cyclizations
  The Journal of Organic Chemistry, 1994
• Synthetic Studies toward Ciguatoxin. Stereocontrolled Construction of the KLM Ring Fragment
  The Journal of Organic Chemistry, 1994
• Synthesis of the AB Ring Fragment of Ciguatoxin: Ligand Controlled Regioselective Addition of Osmium Tetroxide to Double Bonds
  Synlett, 1992
• Application of the dibenzoate chirality method to determine the absolute configuration of glycerols and related acyclic alcohols
  The Journal of Organic Chemistry, 1990