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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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Publication details

The article was received on 28 Dec 2016, accepted on 20 Jan 2017 and first published on 20 Jan 2017


Article type: Communication
DOI: 10.1039/C6CC10288C
Citation: Chem. Commun., 2017,53, 2118-2121
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    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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