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Updated: Jan 11, 2026

Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions
Published on: November 30, 2022
NHC-Boryl Radical-Catalyzed [3 + 2] Cycloaddition for the Synthesis of Vinylcyclopentanes
Yee Lin Phang1, Yan Liu1, Jie Wang1
1State Key Laboratory of Precision and Intelligent Chemistry, Anhui Provincial Key Laboratory of Biomass Chemistry, Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, China.
Abstract:
Heteroatom-centered radicals have recently found important applications in catalyzing a series of radical transformations. Herein, we report a benzimidazolium-based N-heterocyclic carbene (NHC)-boryl radical-catalyzed [3 + 2] cycloaddition between vinylcyclopropanes and alkenes. Such a covalent radical catalysis process features radical addition, cyclopropane ring opening, intermolecular radical addition, ring cyclization, and radical elimination steps to deliver vinylcyclopentanes with good yields and substrate scope.
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