A new synthesis of isoamethyrins: A 4+2 route-Reference-Cited by-同舟云学术

A new synthesis of isoamethyrins: A 4+2 route

Published:2016-08 Issue:08n11 Volume:20 Page:1055-1059
ISSN:1088-4246
Container-title:Journal of Porphyrins and Phthalocyanines
language:en
Short-container-title:J. Porphyrins Phthalocyanines

Author:

Anguera Gonzalo¹,Borrós Salvador¹,Borrell José I.²,Sánchez-García David¹

Affiliation:

1. Grup d’Enginyeria de Materials (GEMAT), Institut Químic de Sarrià, Universitat Ramon Llull, Via Augusta 390, 08017 Barcelona, Spain

2. Grup d’Enginyeria Molecular, Institut Químic de Sarrià, Universitat Ramon Llull, Via Augusta 390, 08017 Barcelona, Spain

Abstract

A concise and versatile strategy for the preparation of isoamethyrins is presented. The novel procedure is predicated on the acid catalyzed condensation of a quaterpyrrole and a bipyrrole dialdehyde. As application of this procedure an aryl substituted isoamethyrin has been synthetized and characterized.

Publisher

World Scientific Pub Co Pte Lt

Subject

General Chemistry

Link

https://www.worldscientific.com/doi/pdf/10.1142/S1088424616500553

Reference26 articles.

1. Synthetic Expanded Porphyrin Chemistry

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3. Effect of the Meso-Substituent in the Hückel-to-Möbius Topological Switches

4. Hückel and Möbius Expandedpara-Benziporphyrins: Synthesis and Aromaticity Switching

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