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Copper catalysis with redox-active ligands
Copper catalysis finds applications in various synthetic fields by utilizing the ability of copper to sustain mono- and bielectronic elementary steps. Further to the development of well-defined copper complexes with classical ligands such as phosphines and N-heterocyclic carbenes, a new and fast-exp...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214867/ https://www.ncbi.nlm.nih.gov/pubmed/32461767 http://dx.doi.org/10.3762/bjoc.16.77 |
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author | Das, Agnideep Ren, Yufeng Hessin, Cheriehan Desage-El Murr, Marine |
author_facet | Das, Agnideep Ren, Yufeng Hessin, Cheriehan Desage-El Murr, Marine |
author_sort | Das, Agnideep |
collection | PubMed |
description | Copper catalysis finds applications in various synthetic fields by utilizing the ability of copper to sustain mono- and bielectronic elementary steps. Further to the development of well-defined copper complexes with classical ligands such as phosphines and N-heterocyclic carbenes, a new and fast-expanding area of research is exploring the possibility of a complementing metal-centered reactivity with electronic participation by the coordination sphere. To achieve this electronic flexibility, redox-active ligands can be used to engage in a fruitful “electronic dialogue” with the metal center, and provide additional venues for electron transfer. This review aims to present the latest results in the area of copper-based cooperative catalysis with redox-active ligands. |
format | Online Article Text |
id | pubmed-7214867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-72148672020-05-26 Copper catalysis with redox-active ligands Das, Agnideep Ren, Yufeng Hessin, Cheriehan Desage-El Murr, Marine Beilstein J Org Chem Review Copper catalysis finds applications in various synthetic fields by utilizing the ability of copper to sustain mono- and bielectronic elementary steps. Further to the development of well-defined copper complexes with classical ligands such as phosphines and N-heterocyclic carbenes, a new and fast-expanding area of research is exploring the possibility of a complementing metal-centered reactivity with electronic participation by the coordination sphere. To achieve this electronic flexibility, redox-active ligands can be used to engage in a fruitful “electronic dialogue” with the metal center, and provide additional venues for electron transfer. This review aims to present the latest results in the area of copper-based cooperative catalysis with redox-active ligands. Beilstein-Institut 2020-04-24 /pmc/articles/PMC7214867/ /pubmed/32461767 http://dx.doi.org/10.3762/bjoc.16.77 Text en Copyright © 2020, Das et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Review Das, Agnideep Ren, Yufeng Hessin, Cheriehan Desage-El Murr, Marine Copper catalysis with redox-active ligands |
title | Copper catalysis with redox-active ligands |
title_full | Copper catalysis with redox-active ligands |
title_fullStr | Copper catalysis with redox-active ligands |
title_full_unstemmed | Copper catalysis with redox-active ligands |
title_short | Copper catalysis with redox-active ligands |
title_sort | copper catalysis with redox-active ligands |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214867/ https://www.ncbi.nlm.nih.gov/pubmed/32461767 http://dx.doi.org/10.3762/bjoc.16.77 |
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