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Cross-dehydrogenative N–N couplings

The relatively high electronegativity of nitrogen makes N–N bond forming cross-coupling reactions particularly difficult, especially in an intermolecular fashion. The challenge increases even further when considering the case of dehydrogenative N–N coupling reactions, which are advantageous in terms...

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Detalles Bibliográficos
Autores principales: Tabey, Alexis, Vemuri, Pooja Y., Patureau, Frederic W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580018/
https://www.ncbi.nlm.nih.gov/pubmed/34880984
http://dx.doi.org/10.1039/d1sc03851f
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author Tabey, Alexis
Vemuri, Pooja Y.
Patureau, Frederic W.
author_facet Tabey, Alexis
Vemuri, Pooja Y.
Patureau, Frederic W.
author_sort Tabey, Alexis
collection PubMed
description The relatively high electronegativity of nitrogen makes N–N bond forming cross-coupling reactions particularly difficult, especially in an intermolecular fashion. The challenge increases even further when considering the case of dehydrogenative N–N coupling reactions, which are advantageous in terms of step and atom economy, but introduce the problem of the oxidant in order to become thermodynamically feasible. Indeed, the oxidizing system must be designed to activate the target N–H bonds, while at the same time avoid undesired N–N homocoupling as well as C–N and C–C coupled side products. Thus, preciously few intermolecular hetero N–N cross-dehydrogenative couplings exist, in spite of the central importance of N–N bonds in organic chemistry. This review aims at analyzing these few rare cases and provides a perspective for future developments.
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spelling pubmed-85800182021-12-07 Cross-dehydrogenative N–N couplings Tabey, Alexis Vemuri, Pooja Y. Patureau, Frederic W. Chem Sci Chemistry The relatively high electronegativity of nitrogen makes N–N bond forming cross-coupling reactions particularly difficult, especially in an intermolecular fashion. The challenge increases even further when considering the case of dehydrogenative N–N coupling reactions, which are advantageous in terms of step and atom economy, but introduce the problem of the oxidant in order to become thermodynamically feasible. Indeed, the oxidizing system must be designed to activate the target N–H bonds, while at the same time avoid undesired N–N homocoupling as well as C–N and C–C coupled side products. Thus, preciously few intermolecular hetero N–N cross-dehydrogenative couplings exist, in spite of the central importance of N–N bonds in organic chemistry. This review aims at analyzing these few rare cases and provides a perspective for future developments. The Royal Society of Chemistry 2021-10-19 /pmc/articles/PMC8580018/ /pubmed/34880984 http://dx.doi.org/10.1039/d1sc03851f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Tabey, Alexis
Vemuri, Pooja Y.
Patureau, Frederic W.
Cross-dehydrogenative N–N couplings
title Cross-dehydrogenative N–N couplings
title_full Cross-dehydrogenative N–N couplings
title_fullStr Cross-dehydrogenative N–N couplings
title_full_unstemmed Cross-dehydrogenative N–N couplings
title_short Cross-dehydrogenative N–N couplings
title_sort cross-dehydrogenative n–n couplings
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580018/
https://www.ncbi.nlm.nih.gov/pubmed/34880984
http://dx.doi.org/10.1039/d1sc03851f
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