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Preparation of cyclic imides from alkene-tethered amides: application of homogeneous Cu(ii) catalytic systems
A Cu-based homogeneous catalytic system was proposed for the preparation of imides from alkene-tethered amides. Here, O(2) acted as a terminal oxidant and a cheap and easily available oxygen source. The cleavage of C[double bond, length as m-dash]C bonds and the formation of C–N bonds were catalyzed...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049870/ https://www.ncbi.nlm.nih.gov/pubmed/35492186 http://dx.doi.org/10.1039/c9ra10422d |
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author | Liu, Zhenghui Wang, Peng Ou, Hualin Yan, Zhenzhong Chen, Suqing Tan, Xingxing Yu, Dongkun Zhao, Xinhui Mu, Tiancheng |
author_facet | Liu, Zhenghui Wang, Peng Ou, Hualin Yan, Zhenzhong Chen, Suqing Tan, Xingxing Yu, Dongkun Zhao, Xinhui Mu, Tiancheng |
author_sort | Liu, Zhenghui |
collection | PubMed |
description | A Cu-based homogeneous catalytic system was proposed for the preparation of imides from alkene-tethered amides. Here, O(2) acted as a terminal oxidant and a cheap and easily available oxygen source. The cleavage of C[double bond, length as m-dash]C bonds and the formation of C–N bonds were catalyzed by Cu(ii) salts with proper nitrogen-containing ligands under 100 °C. The synthesis approach has potential applications in pharmaceutical syntheses. Moreover, scaled-up experiments confirmed the practical applicability. |
format | Online Article Text |
id | pubmed-9049870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90498702022-04-29 Preparation of cyclic imides from alkene-tethered amides: application of homogeneous Cu(ii) catalytic systems Liu, Zhenghui Wang, Peng Ou, Hualin Yan, Zhenzhong Chen, Suqing Tan, Xingxing Yu, Dongkun Zhao, Xinhui Mu, Tiancheng RSC Adv Chemistry A Cu-based homogeneous catalytic system was proposed for the preparation of imides from alkene-tethered amides. Here, O(2) acted as a terminal oxidant and a cheap and easily available oxygen source. The cleavage of C[double bond, length as m-dash]C bonds and the formation of C–N bonds were catalyzed by Cu(ii) salts with proper nitrogen-containing ligands under 100 °C. The synthesis approach has potential applications in pharmaceutical syntheses. Moreover, scaled-up experiments confirmed the practical applicability. The Royal Society of Chemistry 2020-02-21 /pmc/articles/PMC9049870/ /pubmed/35492186 http://dx.doi.org/10.1039/c9ra10422d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Liu, Zhenghui Wang, Peng Ou, Hualin Yan, Zhenzhong Chen, Suqing Tan, Xingxing Yu, Dongkun Zhao, Xinhui Mu, Tiancheng Preparation of cyclic imides from alkene-tethered amides: application of homogeneous Cu(ii) catalytic systems |
title | Preparation of cyclic imides from alkene-tethered amides: application of homogeneous Cu(ii) catalytic systems |
title_full | Preparation of cyclic imides from alkene-tethered amides: application of homogeneous Cu(ii) catalytic systems |
title_fullStr | Preparation of cyclic imides from alkene-tethered amides: application of homogeneous Cu(ii) catalytic systems |
title_full_unstemmed | Preparation of cyclic imides from alkene-tethered amides: application of homogeneous Cu(ii) catalytic systems |
title_short | Preparation of cyclic imides from alkene-tethered amides: application of homogeneous Cu(ii) catalytic systems |
title_sort | preparation of cyclic imides from alkene-tethered amides: application of homogeneous cu(ii) catalytic systems |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049870/ https://www.ncbi.nlm.nih.gov/pubmed/35492186 http://dx.doi.org/10.1039/c9ra10422d |
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