Preparation of 1H-2,3,4,5-tetraarylpyrroles by oxidation of heterocyclic imine-enamines

Article abstract of DOI:10.1080/00397919608086755

Heterocyclic imine-enamines 1 were prepared from metalated methyl substituted heterocycles and aromatic nitriles and then oxidized with lead tetracetate to give various tetraarylpyrroles 2.

Full text of DOI:10.1080/00397919608086755

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Preparation of 1H-2,3,4,5-
Tetraarylpyrroles by oxidation
of heterocyclic imine-enamines
J. Lehuede a , Y. Mettey a & J-M. Vierfond a
a Laboratoire de Chimie Organique (GREAM), Faculté
de Médecine et de Pharmacie , BP 199, 34, rue du
Jardin des Plantes, 86005, Poitiers, France
Published online: 21 Nov 2007.
To cite this article: J. Lehuede , Y. Mettey & J-M. Vierfond (1996) Preparation of
1H-2,3,4,5-Tetraarylpyrroles by oxidation of heterocyclic imine-enamines, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 26:4, 793-802, DOI: 10.1080/00397919608086755
To link to this article: http://dx.doi.org/10.1080/00397919608086755
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