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Benzyl {2-[(2-(1H-Benzo[d][1,2,3]triazol-1-yl)-2-oxoethyl)amino]-2-oxoethyl} carbamate
Molbank 2014, 2014(3), M829; doi:10.3390/M829
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1, 1,* , 1, 1, 2 and 1,*
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
In memory of Prof. Dr. Alan Roy Katritzky.
* Authors to whom correspondence should be addressed.
Received: 1 April 2014 / Accepted: 4 July 2014 / Published: 11 July 2014
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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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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.

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