Literature DB >> 12465920

Synthesis of corroles bearing up to three different meso substituents.

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


  3 in total

1.  Boron-complexation strategy for use with 1-acyldipyrromethanes.

Authors:  Kannan Muthukumaran; Marcin Ptaszek; Bruce Noll; W Robert Scheidt; Jonathan S Lindsey
Journal:  J Org Chem       Date:  2004-08-06       Impact factor: 4.354

2.  Cellular uptake and anticancer activity of carboxylated gallium corroles.

Authors:  Melanie Pribisko; Joshua Palmer; Robert H Grubbs; Harry B Gray; John Termini; Punnajit Lim
Journal:  Proc Natl Acad Sci U S A       Date:  2016-04-04       Impact factor: 11.205

3.  Synthesis of meso-pyrrole-substituted corroles by condensation of 1,9-diformyldipyrromethanes with pyrrole.

Authors:  Baris Temelli; Pinar Kapci
Journal:  Beilstein J Org Chem       Date:  2022-10-06       Impact factor: 2.544

  3 in total

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