A new synthesis of isoamethyrins: A 4+2 route

Research output: Indexed journal article Articlepeer-review

5 Citations (Scopus)


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.

Original languageEnglish
Pages (from-to)1055-1059
Number of pages5
JournalJournal of Porphyrins and Phthalocyanines
Issue number8-11
Publication statusPublished - 1 Nov 2016


  • 2,2′-bipyrrole
  • expanded porphyrins
  • isoamethyrin
  • quaterpyrrole


Dive into the research topics of 'A new synthesis of isoamethyrins: A 4+2 route'. Together they form a unique fingerprint.

Cite this