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

Valentina Mercalli; Aude Nyadanu; Marie Cordier; Gian Cesare Tron; Laurence Grimaud; Laurent El Kaim

doi:10.1039/c6cc10288c

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

Valentina Mercalli, Aude Nyadanu, Marie Cordier, Gian Cesare Tron, Laurence Grimaud, Laurent El Kaim

Dipartimento di Scienze del Farmaco

Risultato della ricerca: Contributo su rivista › Articolo in rivista › peer review

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.

Lingua originale	Inglese
pagine (da-a)	2118-2121
Numero di pagine	4
Rivista	Chemical Communications
Volume	53
Numero di pubblicazione	13
DOI	https://doi.org/10.1039/c6cc10288c
Stato di pubblicazione	Pubblicato - 2017

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10.1039/c6cc10288c

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title = "N-N bond formation in Ugi processes: from nitric acid to libraries of nitramines",

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.",

author = "Valentina Mercalli and Aude Nyadanu and Marie Cordier and Tron, {Gian Cesare} and Laurence Grimaud and {El Kaim}, Laurent",

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AU - Mercalli, Valentina

AU - Nyadanu, Aude

AU - Cordier, Marie

AU - Tron, Gian Cesare

AU - Grimaud, Laurence

AU - El Kaim, Laurent

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AB - 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.

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U2 - 10.1039/c6cc10288c

DO - 10.1039/c6cc10288c

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

Abstract

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