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.
Articolo in rivista - Articolo scientifico
Alkynones; Annulation; Indoles; Nitrosoarenes;
Alkynones; Annulation; Indoles; Nitrosoarenes; Physical and Theoretical Chemistry; Organic Chemistry; Biochemistry
English
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].
Tibiletti, F; Penoni, A; Palmisano, G; Maspero, A; Nicholas, K; Vaghi, L
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/194295
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