Document Type
Article
Publication Date
8-28-2014
Abstract
β-Nitrocorroles are potentially valuable platforms for the preparation of a wide range of more elaborated corrole derivatives possessing unique chemical functionalities and electronic properties. Here we report our results on the chemical manipulation of a copper 3-NO2-triarylcorrolate using different organic reactions, all involving the reduction of -NO2 to -NH2 at an early stage, followed by further transformations. By way of a β-acylated copper corrolate, a novel corrole derivative bearing an alkyl azide group on the peripheral positions was obtained and exploited in the Huisgen 1,3-dipolar cycloaddition. This journal is © the Partner Organisations 2014.
Publication Source (Journal or Book title)
Organic and Biomolecular Chemistry
First Page
6200
Last Page
6207
Recommended Citation
Stefanelli, M., Mancini, M., Raggio, M., Nardis, S., Fronczek, F., McCandless, G., Smith, K., & Paolesse, R. (2014). 3-NO2-5,10,15-triarylcorrolato-Cu as a versatile platform for synthesis of novel 3-functionalized corrole derivatives. Organic and Biomolecular Chemistry, 12 (32), 6200-6207. https://doi.org/10.1039/c4ob01247j