Issue 2, 2004

Preparation of tripyrrane analogues from resorcinol and 2-methylresorcinol for applications in the synthesis of new benziporphyrin systems

Abstract

Acid catalyzed condensation of resorcinol or 2-methylresorcinol with 2 equiv. of an acetoxymethylpyrrole gave bis(pyrrolylmethyl)benzene derivatives in moderate yields; these afforded a series of novel aromatic benziporphyrins using the MacDonald “3 + 1” methodology.

Graphical abstract: Preparation of tripyrrane analogues from resorcinol and 2-methylresorcinol for applications in the synthesis of new benziporphyrin systems

Article information

Article type
Communication
Submitted
17 Oct 2003
Accepted
13 Nov 2003
First published
08 Dec 2003

Chem. Commun., 2004, 178-179

Preparation of tripyrrane analogues from resorcinol and 2-methylresorcinol for applications in the synthesis of new benziporphyrin systems

K. Miyake and T. D. Lash, Chem. Commun., 2004, 178 DOI: 10.1039/B313229N

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