The Reactions of Phosphonium Ylides and Oxosulfonium Methylide with Sulfenamide Derivatives
- 1 September 1970
- journal article
- research article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 43 (9) , 2870-2873
- https://doi.org/10.1246/bcsj.43.2870
Abstract
It was found that vinyl sulfide derivatives were obtained in good yields by the reactions of carbonyl compounds with α-phenylthioalkylidenetriphenylphosphorane. Phosphorane was prepared by the equimolar reaction of alkylidenetriphenylphosphorane and N-phenylthio-N-methylacetamide. It was established that, differing from the case of alkylidenetriphenylphosphorane, di-methyloxosulfonium methylide reacted with N-phenylthiophthalimide and N-phenylthiosuccin-imide to give N-bis(phenylthio)methylphthalimide and N-bis(phenylthio)methylsuccinimide, re-specitively.Keywords
This publication has 2 references indexed in Scilit:
- Alkyl and aryl sulfenimidesThe Journal of Organic Chemistry, 1969
- Dimethyloxosulfonium Methylide ((CH3)2SOCH2) and Dimethylsulfonium Methylide ((CH3)2SCH2). Formation and Application to Organic SynthesisJournal of the American Chemical Society, 1965