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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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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. |
format | Online Article Text |
id | pubmed-8580018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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