N–N bond formation in Ugi processes: from nitric acid to libraries of nitramines-Reference-Cited by-同舟云学术

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

Published:2017 Issue:13 Volume:53 Page:2118-2121
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Mercalli Valentina¹²³⁴⁵,Nyadanu Aude¹²³⁴⁵,Cordier Marie⁶⁷⁸³²,Tron Gian Cesare⁹¹⁰¹¹¹²,Grimaud Laurence¹³¹⁴¹⁵²¹⁶,El Kaim Laurent¹²³⁴⁵^ORCID

Affiliation:

1. Laboratoire de Synthèse Organique

2. CNRS

3. Ecole Polytechnique

4. ENSTA ParisTech- UMR 7652

5. Université Paris-Saclay

6. Laboratoire de Chimie Moléculaire

7. UMR 9168

8. Department of Chemistry

9. Dipartimento di Scienze del Farmaco

10. Università degli Studi del Piemonte Orientale “A. Avogadro”

11. 28100 Novara

12. Italy

13. Ecole normale supérieure

14. PSL Research University

15. UPMC Univ Paris 06

16. Département de Chimie

Abstract

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

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2017/CC/C6CC10288C

Reference56 articles.

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2. Multicomponent Reactions with Isocyanides

3. Maximizing Synthetic Efficiency: Multi-Component Transformations Lead the Way

4. Recent advances in isocyanide-based multicomponent chemistry

5. The Chemistry of Isocyanides, their MultiComponent Reactions and their Libraries

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