Convergent and stereoselective method for synthesis of O -linked oxepane ring system by intramolecular radical cyclization

This publication has 35 references indexed in Scilit:

• Stereoselective Synthesis of the LM Ring Moiety of Ciguatoxin: Reagent Control of Asymmetric Dihydroxylation
  Chemistry Letters, 1997
• Convergent Synthesis of a Trans-fused 6-7-6 Tricyclic Ether System Based on a Ring-closing Metathesis Reaction
  Synlett, 1997
• Diastereoselective Synthesis of the GH Ring Part of Ciguatoxin
  Synlett, 1997
• Diastereoselective Synthesis of Cyclic Ethers by Radical Cyclization at β-Position of β-Alkoxyacrylates
  Synthetic Communications, 1997
• Stereocontrolled synthesis of the HIJ ring system of ciguatoxin
  Chemical Communications, 1997
• Extensive Ring-Expansion Strategy for the Enantioselective Synthesis of the Medium Ring Ethers, Oxepene, Oxocane, and Oxonene, of Ciguatoxin
  Synlett, 1996
• syn-trans Fused Bicyclic Ether Formation via Acetylene-biscobalthexacarbonyl Complex
  Chemistry Letters, 1996
• Synthetic Studies toward Ciguatoxin. Stereocontrolled Construction of the KLM Ring Fragment
  The Journal of Organic Chemistry, 1994
• Facile Reduction of Dithiocarbonates Derived from Secondary Alcohols with n-Bu3SnH–Et3B and Synthesis of 2-Furanthiones and 2-Furanones by Intramolecular Addition of Alkoxythiocarbonyl Free Radicals to Acetylenic Linkages
  Bulletin of the Chemical Society of Japan, 1990
• Ciguatoxin and brevetoxins share a common receptor site on the neuronal voltage‐dependent Na⁺ channel
  FEBS Letters, 1987