| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275328 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
A new method for the preparation of isocorroles has been developed based on the reaction of triphenylcorrole with DDQ. Regioisomer 7 where the interruption of the conjugation is at the 5 position, is reported for the first time.
Graphical abstractReaction of triarylcorroles with DDQ gives two isocorroles, with the interruption of conjugation at the 5 or 10 position, representing a facile synthetic route for the preparation these macrocycles.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
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