A facile conversion of tetrahydropyranyl ethers to the corresponding bromides and iodides

This publication has 12 references indexed in Scilit:

• Direct conversion of tetrahydropyranylated alcohols to the corresponding bromides
  Tetrahedron Letters, 1989
• A Facile Conversion of α-Nitroepoxides into 1,2-Diones and α-Iodoketones
  Chemistry Letters, 1989
• Activation and synthetic applications of thiostannanes. Chemical modification of hydroxy function under protection
  Tetrahedron Letters, 1989
• 1,2-bis(diphenylphosphino)ethane tetrahalide: A convenient reagent for the conversion of alcohols to the corresponding halides
  Tetrahedron Letters, 1987
• Sodium Iodide-Chlorotrimethylsilane (Or Boron Trifluo-ride Etherate) and Zinc-Chlorotrimethylsilane: Mild Reagent Systems for the Conversion of Enediones Into 1,4–Diketones
  Synthetic Communications, 1987
• Boron Trifluoride Etherate/Iodide Ion, a Novel Reagent for the Non-Aqueous Conversion of Acetals to Carbonyl Compounds
  Synthesis, 1986
• Sodium iodide/boron trifluoride etherate: A mild reagent system for the conversion of allylic and benzylic alcohols into corresponding iodides and sulfoxides into sulfides
  Tetrahedron Letters, 1985
• Direct Conversion of an Alcohol Tetrahydropyranyl Ether to a Bromide, Chloride, Methyl Ether, Nitrile or Trifluoroacetate
  Synthetic Communications, 1976
• Synthesis of 3,11-dimethyl-2-nonacosanone, a sex pheromone of the German cockroach
  The Journal of Organic Chemistry, 1975
• Insect Sex Attractants; XII¹. An Efficient Procedure for the Preparation of Unsaturated Alcohols and Acetates
  Synthesis, 1972