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Benzyl {2-[(2-(1H-Benzo[d][1,2,3]triazol-1-yl)-2-oxoethyl)amino]-2-oxoethyl} carbamate
 
 
Short Note

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

1
Dipartimento di Scienza e Alta Tecnologia, Università degli Studi dell'Insubria, via Valleggio 11, 22100, Como, Italy
2
Department of Chemistry and Biochemistry, University of Oklahoma, Stephenson Life Sciences Research Center, 101 Stephenson Parkway, Norman, OK 73019-5251, USA
*
Authors to whom correspondence should be addressed.
In memory of Prof. Dr. Alan Roy Katritzky.
Molbank 2014, 2014(3), M829; https://doi.org/10.3390/M829
Received: 1 April 2014 / Accepted: 4 July 2014 / Published: 11 July 2014
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. View Full-Text
Keywords: indoles; alkynones; nitrosoarenes; annulation indoles; alkynones; nitrosoarenes; annulation
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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. https://doi.org/10.3390/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. https://doi.org/10.3390/M829

Chicago/Turabian Style

Tibiletti, Francesco, Andrea Penoni, Giovanni Palmisano, Angelo Maspero, Kenneth M. Nicholas, and Luca Vaghi. 2014. "(1H-Benzo[d][1,2,3]triazol-1-yl)(5-bromo-1-hydroxy-1H-indol-3-yl)methanone" Molbank 2014, no. 3: M829. https://doi.org/10.3390/M829

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