The title compound was easily prepared by a nitrosoarene-alkyne cycloaddition reaction carried out in toluene at 80 °C. The product is a highly functionalized compound that can be further derivatized through various functional group interconversion procedures. © 2014 by the authors; licensee MDPI, Basel, Switzerland.
Tibiletti, F., Penoni, A., Palmisano, G., Maspero, A., Nicholas, K., Vaghi, L. (2014). (1H-Benzo[d][1,2,3]triazol-1-yl)(5-bromo-1-hydroxy-1H-indol-3-yl)methanone. MOLBANK, 2014(3) [10.3390/M829].
(1H-Benzo[d][1,2,3]triazol-1-yl)(5-bromo-1-hydroxy-1H-indol-3-yl)methanone
Vaghi, L
2014
Abstract
The title compound was easily prepared by a nitrosoarene-alkyne cycloaddition reaction carried out in toluene at 80 °C. The product is a highly functionalized compound that can be further derivatized through various functional group interconversion procedures. © 2014 by the authors; licensee MDPI, Basel, Switzerland.
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