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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...

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Autores principales: Liu, Zhenghui, Wang, Peng, Ou, Hualin, Yan, Zhenzhong, Chen, Suqing, Tan, Xingxing, Yu, Dongkun, Zhao, Xinhui, Mu, Tiancheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
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.
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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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