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Updated: Feb 12, 2026

Facile Preparation of 2Z,4E-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
Published on: June 21, 2017
Ruthenium(ii)-catalyzed olefination via carbonyl reductive cross-coupling
Wei Wei1,2, Xi-Jie Dai1, Haining Wang1
1Department of Chemistry , FQRNT Center for Green Chemistry and Catalysis , McGill University , 801 Sherbrooke St. W. , Montreal , Quebec H3A 0B8 , Canada .
Abstract:
Natural availability of carbonyl groups offers reductive carbonyl coupling tremendous synthetic potential for efficient olefin synthesis, yet the catalytic carbonyl cross-coupling remains largely elusive. We report herein such a reaction, mediated by hydrazine under ruthenium(ii) catalysis. This method enables facile and selective cross-couplings of two unsymmetrical carbonyl compounds in either an intermolecular or intramolecular fashion. Moreover, this chemistry accommodates a variety of substrates, proceeds under mild reaction conditions with good functional group tolerance, and generates stoichiometric benign byproducts. Importantly, the coexistence of KO Bu and bidentate phosphine dmpe is vital to this transformation.
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