Cascade cyclization/fluoromethylthiolation of alkynes, unsaturated α-bromocarbonyls and PhSO2SRF

Abstract

A copper-catalyzed cyclization/fluoromethylthiolation cascade of alkynes, unsaturated α-bromocarbonyls and PhSO2SCF2H/PhSO2SCF3 has been developed to access fluoromethylthiolated cyclopentenes and cyclohexenes. The present reaction enables the construction of three new chemical bonds in a single step through the addition of alkyl radicals across alkynes, followed by cyclization and fluoromethylthiolation. It is characterized by high chemoselectivity and a broad substrate scope.

Graphical abstract: Cascade cyclization/fluoromethylthiolation of alkynes, unsaturated α-bromocarbonyls and PhSO2SRF

Supplementary files

Article information

Article type
Research Article
Submitted
28 Mar 2025
Accepted
13 May 2025
First published
14 May 2025

Org. Chem. Front., 2025, Advance Article

Cascade cyclization/fluoromethylthiolation of alkynes, unsaturated α-bromocarbonyls and PhSO2SRF

C. Zhang, Y. Shen, N. Xia, X. Zhou, L. Yang, J. Hu and Y. Li, Org. Chem. Front., 2025, Advance Article , DOI: 10.1039/D5QO00585J

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