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

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

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

Fingerprint Dive into the research topics of 'An unusual rearrangement, and further transformations, in the chlorination of alkoxythiocarbonylsulfenyl substrates'. Together they form a unique fingerprint.

Cite this