Journal Article

Synthesis and Bergman cyclization of a β-extended porphyrenediyne

Chemical Communications (2004) 4(2) 180-181
DOI: 10.1039/b312001e
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Abstract

Condensation of a porphyrin-2,3-dione with a 1,2-diaminoarenediyne affords a β-extended porphyrinic-enediyne: upon thermal Bergman cyclization the quinoxaline spacer positioned between the macrocycle and the enediyne prevents tandem radical cyclization to a picenoporphyrin. © 2004 Royal Society of Chemistry.

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APA

Spence, J. D., Cline, E. D., Lagostera, D. M., & O’Toole, P. S. (2004). Synthesis and Bergman cyclization of a β-extended porphyrenediyne. Chemical Communications, 4(2), 180–181. https://doi.org/10.1039/b312001e

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