A Facile Conversion of Tertiary Alcohols to Olefins
- 1 March 1989
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 19 (5-6), 1057-1060
- https://doi.org/10.1080/00397918908051028
Abstract
An efficient method for the dehydration of tertiary alcohols to obtain olefins in high yield, employing methanesulfonyl chloride-triethylamine and catalytic amount of 4-dimethylaminopyridine in dichloromethane, is described.Keywords
This publication has 9 references indexed in Scilit:
- Dimethyl 2,3‐Dimethylenebutanedioate from Methyl Pyruvate and Methyl AcrylateEuropean Journal of Inorganic Chemistry, 1987
- 1,3,5-trideoxy-3,5-di-C-methyl-l-talitol: a chiron for the C-33–C-37 segment of amphotericin BCarbohydrate Research, 1987
- Reactions of hydroxyl groups with tosylchloride-dimethylaminopyridine system. Direct synthesis of chlorides from hydroxycompoundsTetrahedron Letters, 1984
- 4-Dialkylaminopyridines: super acylation and alkylation catalystsChemical Society Reviews, 1983
- Diels–Alder reactions. Part II. Condensation of methyl trans-β-formyl-crotonate with dienols and their acetatesJournal of the Chemical Society, Perkin Transactions 1, 1973
- Sulfuranes. VI. Reactions involving the alkoxy ligands of dialkoxydiarylsulfuranes. Formation of olefins and ethersJournal of the American Chemical Society, 1972
- Synthetic applications of N-carboalkoxysulfamate estersJournal of the American Chemical Society, 1970
- Pyrolytic Cis Eliminations.Chemical Reviews, 1960
- A New Method for the Preparation of 17(α)-Hydroxy-20-ketopregnanesJournal of the American Chemical Society, 1948