Triarylborane-Catalyzed Alkenylation Reactions of Aryl Esters with Diazo Compounds

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Abstract

Herein we report a facile, mild reaction protocol to form carbon–carbon bonds in the absence of transition metal catalysts. We demonstrate the metal-free alkenylation reactions of aryl esters with α-diazoesters to give highly functionalized enyne products. Catalytic amounts of tris(pentafluorophenyl)borane (10–20 mol %) are employed to afford the C=C coupled products (31 examples) in good to excellent yields (36–87 %). DFT studies were used to elucidate the mechanism for this alkenylation reaction.

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Dasgupta, A., Stefkova, K., Babaahmadi, R., Gierlichs, L., Ariafard, A., & Melen, R. L. (2020). Triarylborane-Catalyzed Alkenylation Reactions of Aryl Esters with Diazo Compounds. Angewandte Chemie - International Edition, 59(36), 15492–15496. https://doi.org/10.1002/anie.202007176

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