A new, highly efficient method for the conversion of alcohols to thiolesters and thiols
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (33) , 3119-3122
- https://doi.org/10.1016/s0040-4039(01)81842-6
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural ProductsSynthesis, 1981
- NEW SYNTHETIC REACTIONS BASED ON 1-METHYL-2-FLUOROPYRIDINIUM SALTS. STEREOSPECIFIC PREPARATION OF THIOALCOHOLS FROM ALCOHOLSChemistry Letters, 1977
- NEW SYNTHETIC REACTIONS BASED ON 1-METHYL-2-FLUOROPYRIDINIUM SALTS. FACILE CONVERSION OF ALCOHOLS TO THIOALCOHOLSChemistry Letters, 1977
- Oxidation‐Reduction CondensationAngewandte Chemie International Edition in English, 1976
- A Mild Synthesis of Optically Active ThiolsSynthesis, 1974
- Stereospecific and stereoselective reactions. I. Preparation of amines from alcoholsJournal of the American Chemical Society, 1972
- Preparation of Carboxylic Esters and Phosphoric Esters by the Activation of AlcoholsBulletin of the Chemical Society of Japan, 1971
- Preparation of Esters of Carboxylic and Phosphoric Acid via Quaternary Phosphonium SaltsBulletin of the Chemical Society of Japan, 1967
- 579. The preparation, via thiuronium salts, of optically active thiolsJournal of the Chemical Society, 1956
- Optical rotation and atomic dimension. Experimental progress on the walden inversionRecueil des Travaux Chimiques des Pays-Bas, 1946