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 language | English |
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Pages (from-to) | 1055-1059 |
Number of pages | 5 |
Journal | Journal of Porphyrins and Phthalocyanines |
Volume | 20 |
Issue number | 8-11 |
DOIs | |
Publication status | Published - 1 Nov 2016 |
Keywords
- 2,2′-bipyrrole
- expanded porphyrins
- isoamethyrin
- quaterpyrrole