AbstractThe 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.
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Tibiletti, F.; Penoni, A.; Palmisano, G.; Maspero, A.; Nicholas, K.M.; Vaghi, L. (1H-Benzo[d][1,2,3]triazol-1-yl)(5-bromo-1-hydroxy-1H-indol-3-yl)methanone. Molbank 2014, 2014, M829.
Tibiletti F, Penoni A, Palmisano G, Maspero A, Nicholas KM, Vaghi L. (1H-Benzo[d][1,2,3]triazol-1-yl)(5-bromo-1-hydroxy-1H-indol-3-yl)methanone. Molbank. 2014; 2014(3):M829.Chicago/Turabian Style
Tibiletti, Francesco; Penoni, Andrea; Palmisano, Giovanni; Maspero, Angelo; Nicholas, Kenneth M.; Vaghi, Luca. 2014. "(1H-Benzo[d][1,2,3]triazol-1-yl)(5-bromo-1-hydroxy-1H-indol-3-yl)methanone." Molbank 2014, no. 3: M829.
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