4.6 Article

Aerobic oxysulfonylation of alkenes using thiophenols: an efficient one-pot route to β-ketosulfones

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 12, Issue 42, Pages 8550-8554

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ob00776j

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Funding

  1. CSIR [09/001(0379)/2013-EMR-I]

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We have developed a highly efficient synthetic route to beta-ketosuifones via AgNO3 catalyzed oxysulfonylation of alkenes using thiophenols in the presence of air (O-2) and K2S2O8 as eco-friendly oxidants. Thiophenols have been used as sulfonylation precursors for the first time in a dioxygen activation based radical process. Moreover, the protocol also offers a new and convenient method for the synthesis of beta-hydroxysulfides at room temperature without the use of any initiator.

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