4.1 Article

Mild and efficient access to lithium alkanesulfinates based on oxaziridine-promoted oxidation of thiolates

Journal

JOURNAL OF SULFUR CHEMISTRY
Volume 30, Issue 3-4, Pages 338-345

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/17415990902903009

Keywords

oxidation; oxaziridine; thiolate; sulfinate; sulfone

Funding

  1. CNRS (Centre National de la Recherche Scientifique)
  2. Region Basse-Normandie
  3. European Union

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Lithium alkanethiolates do not react with N-sulfonyloxaziridine 1 to generate sulfenate species, as uniformly reported in other series. In the present case, a double oxidation reaction is exclusively observed. This unexpected outcome was then exploited for a general, mild and straightforward route to aliphatic sulfinate salts. Investigation of further transformation into sulfones is also described.

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