ArticleChemistry (Weinheim an der Bergstrasse, Germany)2026
Gold Redox Catalysis Enabled by Cyclic Diacyl Peroxides for Homocoupling and Cross-Coupling of Terminal Alkynes.
Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Conjugated 1,3-diynes are valuable scaffolds, yet their selective assembly via cross-coupling of terminal alkynes remains challenging. In this study, we report a gold redox catalytic system employing cyclic diacyl peroxides as dual-function oxidants that enable both homocoupling and cross-coupling of terminal alkynes without exogenous ligands. This operationally simple protocol proceeds under mild conditions, exhibits broad substrate scope, and delivers symmetrical and unsymmetrical 1,3-diynes in moderate to good yields. The tether-guided redox platform facilitates efficient Au(I)/Au(III) redox cycling, offering a previously unrecognized catalytic paradigm to ligand-free gold catalysis for selective C(sp)─C(sp) bond formation.
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