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Issue 13, 2017
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N–N bond formation in Ugi processes: from nitric acid to libraries of nitramines

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Abstract

The Ugi reaction has drawn considerable attention over the years leading to numerous libraries of heterocycles and various extensions changing the nature of the components of the coupling. We report here the use of nitric acid as carboxylic acids surrogates, displaying the first aminative Ugi-type reaction leading to nitramines.

Graphical abstract: N–N bond formation in Ugi processes: from nitric acid to libraries of nitramines

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Supplementary files

Article information


Submitted
28 Dec 2016
Accepted
20 Jan 2017
First published
20 Jan 2017

Chem. Commun., 2017,53, 2118-2121
Article type
Communication

N–N bond formation in Ugi processes: from nitric acid to libraries of nitramines

V. Mercalli, A. Nyadanu, M. Cordier, G. C. Tron, L. Grimaud and L. El Kaim, Chem. Commun., 2017, 53, 2118
DOI: 10.1039/C6CC10288C

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