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Molbank 2014, 2014(3), M829; doi:10.3390/M829
Short Note

(1H-Benzo[d][1,2,3]triazol-1-yl)(5-bromo-1-hydroxy-1H-indol-3-yl)methanone

1, 1,* , 1, 1, 2 and 1,*
Received: 1 April 2014; Accepted: 4 July 2014 / Published: 11 July 2014
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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.
Keywords: indoles; alkynones; nitrosoarenes; annulation indoles; alkynones; nitrosoarenes; annulation
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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MDPI and ACS Style

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.

AMA Style

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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