The evolution of corrole synthesis — from simple one-pot strategies to sophisticated ABC-corroles-Reference-Cited by-同舟云学术

The evolution of corrole synthesis — from simple one-pot strategies to sophisticated ABC-corroles

Published:2016-01 Issue:01n04 Volume:20 Page:96-107
ISSN:1088-4246
Container-title:Journal of Porphyrins and Phthalocyanines
language:en
Short-container-title:J. Porphyrins Phthalocyanines

Author:

König Michael¹,Faschinger Felix²,Reith Lorenz Michael³,Schöfberger Wolfgang⁴

Affiliation:

1. Institute of Polymer Chemistry, Johannes Kepler University Linz (JKU), Altenberger Straße 69, A-4040 Linz, Austria

2. Institute of Biophysics, Johannes Kepler University Linz (JKU), Gruberstraße 40, A-4020 Linz, Austria

3. ENGEL AUSTRIA GmbH, Ludwig-Engel-Strasse 1, 4311 Schwertberg, Austria

4. Institute of Organic Chemistry, Johannes Kepler University Linz (JKU), Altenberger Straße 69, A-4040 Linz, Austria

Abstract

This review highlights synthesis procedures to obtain A3-, cis- and trans- A2B- and ABC-corroles. Synthesis methods from the early beginning of “corrole chemistry”, acid-catalyzed condensation methods of various building blocks (pyrrole, aldehyde, dipyrromethane, dipyrromethane-carbinol, and dipyrromethane-dicarbinol etc.), possible side reaction during Brønsted acid catalyzed reactions (scrambling), one-pot synthesis of corroles, and post-macrocyclization modification reactions of meso-substituted A3-corroles are discussed.

Publisher

World Scientific Pub Co Pte Lt

Subject

General Chemistry

Link

https://www.worldscientific.com/doi/pdf/10.1142/S1088424616300056

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4. Adventures in the synthesis of meso-substituted corroles

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