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

doi:10.1016/S0040-4039(00)79948-5

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

CLAS-NS: Molecular Sciences, School of (SMS)

Research output: Contribution to journal › Article › peer-review

14 Scopus citations

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 language	English (US)
Pages (from-to)	995-998
Number of pages	4
Journal	Tetrahedron Letters
Volume	35
Issue number	7
DOIs	https://doi.org/10.1016/S0040-4039(00)79948-5
State	Published - Feb 14 1994

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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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.",

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AU - Demanche, Lori J.

AU - Li, Shumin

AU - Macpherson, Alisdair N.

AU - Nieman, Ronald A.

AU - Moore, Ana

AU - Moore, Thomas

AU - Gust, Devens

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