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

Research output: Contribution to journal › Article › 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.

Original language	English
Pages (from-to)	2118-2121
Number of pages	4
Journal	Chemical Communications
Volume	53
Issue number	13
DOIs	https://doi.org/10.1039/c6cc10288c
Publication status	Published - 1 Jan 2017
Externally published	Yes

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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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doi = "10.1039/c6cc10288c",

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AU - Mercalli, Valentina

AU - Nyadanu, Aude

AU - Cordier, Marie

AU - Tron, Gian Cesare

AU - Grimaud, Laurence

AU - El Kaim, Laurent

N1 - Publisher Copyright: © The Royal Society of Chemistry.

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Y1 - 2017/1/1

N2 - 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.

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.

UR - https://www.scopus.com/pages/publications/85012195472

U2 - 10.1039/c6cc10288c

DO - 10.1039/c6cc10288c

M3 - Article

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AN - SCOPUS:85012195472

SN - 1359-7345

VL - 53

SP - 2118

EP - 2121

JO - Chemical Communications

JF - Chemical Communications

IS - 13

ER -

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

Abstract

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