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 L Moore, Thomas A Moore, John Devens Gust

Research output: Contribution to journalArticle

14 Citations (Scopus)

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
Pages (from-to)995-998
Number of pages4
JournalTetrahedron Letters
Volume35
Issue number7
DOIs
Publication statusPublished - Feb 14 1994

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Porphyrins
Cycloaddition Reaction
Derivatives
Joining
Functional groups

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

A new porphyrin derivative for use as a diene in the Diels-Alder reaction. / Liddell, Paul A.; Demanche, Lori J.; Li, Shumin; Macpherson, Alisdair N.; Nieman, Ronald A.; Moore, Ana L; Moore, Thomas A; Gust, John Devens.

In: Tetrahedron Letters, Vol. 35, No. 7, 14.02.1994, p. 995-998.

Research output: Contribution to journalArticle

Liddell, Paul A. ; Demanche, Lori J. ; Li, Shumin ; Macpherson, Alisdair N. ; Nieman, Ronald A. ; Moore, Ana L ; Moore, Thomas A ; Gust, John Devens. / A new porphyrin derivative for use as a diene in the Diels-Alder reaction. In: Tetrahedron Letters. 1994 ; Vol. 35, No. 7. pp. 995-998.
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