An unusual rearrangement, and further transformations, in the chlorination of alkoxythiocarbonylsulfenyl substrates

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Abstract

Treatment of alkoxythiocarbonylsulfenyl substrates with one equiv. of sulfuryl chloride, expected to provide alkoxychlorothiochloromethylsulfenyl derivatives, gave directly alkoxydichloromethyldisulfanyl products via a rapid intramolecular rearrangement.

Original languageEnglish (US)
Pages (from-to)5683-5686
Number of pages4
JournalTetrahedron Letters
Volume24
Issue number51
DOIs
StatePublished - 1983

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