Supersizing pyrrole-modified porphyrins by reversal of the 'breaking and mending' strategy

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Abstract

While the 'breaking and mending of porphyrin strategy' proved versatile in the generation of a range of pyrrole-modified porphyrins containing 4-, 5-, and 6-membered heterocycles, it failed to access systems incorporating larger rings. A reversal of the strategy-first mending, then breaking-now allowed the formation of a pyrrole-modified porphyrin containing an 8-membered 1,3,6-triazocine-2,4,8-trione heterocycle.

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Luciano, M., Tardie, W., Zeller, M., & Brückner, C. (2016). Supersizing pyrrole-modified porphyrins by reversal of the “breaking and mending” strategy. Chemical Communications, 52(66), 10133–10136. https://doi.org/10.1039/c6cc04028d

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