A new synthesis of isoamethyrins: A 4+2 route

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5 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)1055-1059
Number of pages5
JournalJournal of Porphyrins and Phthalocyanines
Volume20
Issue number8-11
DOIs
Publication statusPublished - 1 Nov 2016

Keywords

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

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