Abstract
-
O-Alkyl S-methyl dithiocarbonates react with trimethyltin radicals to afford alkoxythiocarbonyl radicals which undergo slow β-fission to alkyl radicals and carbon oxysulphide.
E.S.R. identification of alkoxythiocarbonyl radicals as possible intermediates in Barton deoxygenation of alcohols
Journal ArticleOverview
UOW Authors
Publication Date
- 1984
Publisher
Published In
Background
Citation
- Barker, P. J., & Beckwith, A. L. J. (1984). E.S.R. identification of alkoxythiocarbonyl radicals as possible intermediates in Barton deoxygenation of alcohols. Journal of the Chemical Society, Chemical Communications, (11), 683-684. doi:10.1039/c39840000683
Identity
Digital Object Identifier (doi)
Scopus Eid
- 2-s2.0-37049097820
Web Of Science Accession Number
Additional Document Info
Start Page
- 683
End Page
- 684
Issue
- 11
Overview
Abstract
-
O-Alkyl S-methyl dithiocarbonates react with trimethyltin radicals to afford alkoxythiocarbonyl radicals which undergo slow β-fission to alkyl radicals and carbon oxysulphide.
UOW Authors
Publication Date
- 1984
Publisher
Published In
Background
Citation
- Barker, P. J., & Beckwith, A. L. J. (1984). E.S.R. identification of alkoxythiocarbonyl radicals as possible intermediates in Barton deoxygenation of alcohols. Journal of the Chemical Society, Chemical Communications, (11), 683-684. doi:10.1039/c39840000683
Identity
Digital Object Identifier (doi)
Scopus Eid
- 2-s2.0-37049097820
Web Of Science Accession Number
Additional Document Info
Start Page
- 683
End Page
- 684
Issue
- 11