Preferential formation of cyclic trimers by palladium-catalyzed oxidative coupling reactions of 2,18-diethynylporphyrins

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Abstract

And palladium makes three: In contrast to the formation of cyclic dimers in the Cu-mediated reaction, Pd-catalyzed oxidative coupling of 2,18-diethynylporphyrins preferentially produced cyclic trimers (see scheme). A porphyrin hexamer with a doubly 1,3-butadiyne-bridged conjugated trimeric core and directly meso-appended peripheral porphyrin substituents was also synthesized. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Tokuji, S., Yorimitsu, H., & Osuka, A. (2012). Preferential formation of cyclic trimers by palladium-catalyzed oxidative coupling reactions of 2,18-diethynylporphyrins. Angewandte Chemie - International Edition, 51(49), 12357–12361. https://doi.org/10.1002/anie.201207763

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