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C–H bond halogenation catalyzed or mediated by copper: an overview
Carbon–halogen (C–X) bonds are amongst the most fundamental groups in organic synthesis, they are frequently and widely employed in the synthesis of numerous organic products. The generation of a C–X bond, therefore, constitutes an issue of universal interest. Herein, the research advances on the co...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661017/ https://www.ncbi.nlm.nih.gov/pubmed/26664634 http://dx.doi.org/10.3762/bjoc.11.230 |
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author | Hao, Wenyan Liu, Yunyun |
author_facet | Hao, Wenyan Liu, Yunyun |
author_sort | Hao, Wenyan |
collection | PubMed |
description | Carbon–halogen (C–X) bonds are amongst the most fundamental groups in organic synthesis, they are frequently and widely employed in the synthesis of numerous organic products. The generation of a C–X bond, therefore, constitutes an issue of universal interest. Herein, the research advances on the copper-catalyzed and mediated C–X (X = F, Cl, Br, I) bond formation via direct C–H bond transformation is reviewed. |
format | Online Article Text |
id | pubmed-4661017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-46610172015-12-09 C–H bond halogenation catalyzed or mediated by copper: an overview Hao, Wenyan Liu, Yunyun Beilstein J Org Chem Review Carbon–halogen (C–X) bonds are amongst the most fundamental groups in organic synthesis, they are frequently and widely employed in the synthesis of numerous organic products. The generation of a C–X bond, therefore, constitutes an issue of universal interest. Herein, the research advances on the copper-catalyzed and mediated C–X (X = F, Cl, Br, I) bond formation via direct C–H bond transformation is reviewed. Beilstein-Institut 2015-11-09 /pmc/articles/PMC4661017/ /pubmed/26664634 http://dx.doi.org/10.3762/bjoc.11.230 Text en Copyright © 2015, Hao and Liu 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 Hao, Wenyan Liu, Yunyun C–H bond halogenation catalyzed or mediated by copper: an overview |
title | C–H bond halogenation catalyzed or mediated by copper: an overview |
title_full | C–H bond halogenation catalyzed or mediated by copper: an overview |
title_fullStr | C–H bond halogenation catalyzed or mediated by copper: an overview |
title_full_unstemmed | C–H bond halogenation catalyzed or mediated by copper: an overview |
title_short | C–H bond halogenation catalyzed or mediated by copper: an overview |
title_sort | c–h bond halogenation catalyzed or mediated by copper: an overview |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661017/ https://www.ncbi.nlm.nih.gov/pubmed/26664634 http://dx.doi.org/10.3762/bjoc.11.230 |
work_keys_str_mv | AT haowenyan chbondhalogenationcatalyzedormediatedbycopperanoverview AT liuyunyun chbondhalogenationcatalyzedormediatedbycopperanoverview |