| Literature DB >> 12465920 |
Roger Guilard1, Daniel T Gryko, Gabriel Canard, Jean-Michel Barbe, Beata Koszarna, Stéphane Brandès, Mariusz Tasior.
Abstract
[reaction: see text] We have developed a new method that affords regioisomerically pure corroles possessing up to three different substituents at the meso positions. The corrole formation reaction involves the acid-catalyzed condensation of a dipyrromethane-dicarbinol with pyrrole followed by oxidation with DDQ. ABC-Type corroles were synthesized for the first time according to this procedure.Entities:
Year: 2002 PMID: 12465920 DOI: 10.1021/ol027003w
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005