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Recent advances in copper-catalyzed C–H bond amidation
Copper catalysis has been known as a powerful tool for its ubiquitous application in organic synthesis. One of the fundamental utilities of copper catalysis is in the C–N bond formation by using carbon sources and nitrogen functional groups such as amides. In this review, the recent progress in the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660963/ https://www.ncbi.nlm.nih.gov/pubmed/26664644 http://dx.doi.org/10.3762/bjoc.11.240 |
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author | Wan, Jie-Ping Jing, Yanfeng |
author_facet | Wan, Jie-Ping Jing, Yanfeng |
author_sort | Wan, Jie-Ping |
collection | PubMed |
description | Copper catalysis has been known as a powerful tool for its ubiquitous application in organic synthesis. One of the fundamental utilities of copper catalysis is in the C–N bond formation by using carbon sources and nitrogen functional groups such as amides. In this review, the recent progress in the amidation reactions employing copper-catalyzed C–H amidation is summarized. |
format | Online Article Text |
id | pubmed-4660963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-46609632015-12-09 Recent advances in copper-catalyzed C–H bond amidation Wan, Jie-Ping Jing, Yanfeng Beilstein J Org Chem Review Copper catalysis has been known as a powerful tool for its ubiquitous application in organic synthesis. One of the fundamental utilities of copper catalysis is in the C–N bond formation by using carbon sources and nitrogen functional groups such as amides. In this review, the recent progress in the amidation reactions employing copper-catalyzed C–H amidation is summarized. Beilstein-Institut 2015-11-17 /pmc/articles/PMC4660963/ /pubmed/26664644 http://dx.doi.org/10.3762/bjoc.11.240 Text en Copyright © 2015, Wan and Jing https://creativecommons.org/licenses/by/2.0https://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/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Review Wan, Jie-Ping Jing, Yanfeng Recent advances in copper-catalyzed C–H bond amidation |
title | Recent advances in copper-catalyzed C–H bond amidation |
title_full | Recent advances in copper-catalyzed C–H bond amidation |
title_fullStr | Recent advances in copper-catalyzed C–H bond amidation |
title_full_unstemmed | Recent advances in copper-catalyzed C–H bond amidation |
title_short | Recent advances in copper-catalyzed C–H bond amidation |
title_sort | recent advances in copper-catalyzed c–h bond amidation |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660963/ https://www.ncbi.nlm.nih.gov/pubmed/26664644 http://dx.doi.org/10.3762/bjoc.11.240 |
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