Silver-mediated oxidative C–C bond sulfonylation/arylation of methylenecyclopropanes with sodium sulfinates: facile access to 3-sulfonyl-1,2-dihydronaphthalenes†
Abstract
The novel AgNO3-mediated oxidative sulfonylation/arylation of a C–C σ-bond in methylenecyclopropanes with sodium sulfinates to synthesize various 3-sulfonylated 1,2-dihydronaphthalenes is reported. This sulfonylation/arylation transformation proceeds via a sequence of sulfonylation, C–C σ-bond cleavage and intramolecular cyclization, and the experimental results show that the C–C σ-bond difunctionalization reaction includes a radical process. This strategy provides a simple and convenient route for the difunctionalization of C–C bonds with a phenyl ring and a sulfonyl radical via the one-pot construction of a C–S bond and a new C–C bond.
- This article is part of the themed collection: Synthetic methodology in OBC