A new porphyrin derivative for use as a diene in the Diels-Alder reaction

Paul A. Liddell, Lori J. Demanche, Shumin Li, Alisdair N. Macpherson, Ronald A. Nieman, Ana Moore, Thomas Moore, Devens Gust

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Abstract

The first representative of a new class of porphyrins featuring a tetramethine bridge joining the 2 and 20 positions of the macrocycle has been prepared and found to undergo the Diels-Alder reaction, yielding structures in which functional groups are linked to the porphyrin macrocycle through a rigid, bicyclic bridge.

Original languageEnglish (US)
Pages (from-to)995-998
Number of pages4
JournalTetrahedron Letters
Volume35
Issue number7
DOIs
StatePublished - Feb 14 1994

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ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

Liddell, P. A., Demanche, L. J., Li, S., Macpherson, A. N., Nieman, R. A., Moore, A., Moore, T., & Gust, D. (1994). A new porphyrin derivative for use as a diene in the Diels-Alder reaction. Tetrahedron Letters, 35(7), 995-998. https://doi.org/10.1016/S0040-4039(00)79948-5