Hydrogen bonding in organic synthesis. Part 9. The sulphenylation of fluoride-activated β-dicarbonyls
Open Access
- 1 January 1978
- journal article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 56 (1) , 141-143
- https://doi.org/10.1139/v78-021
Abstract
Various α-arylthio-β-dicarbonyls have been prepared by the room temperature reaction of β-dicarbonyltetraethylammonium fluoride monosolvates with aryl disulphides. The disulphides are formed by the in situ fluoride-assisted air oxidation of aryl thiols.Keywords
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