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Cu(BF(4))(2)/AC-Catalyzed Synthesis of N-Substituted Anilines, N-Substituted 1,6-Naphthyridin-5(6H)-one, and Isoquinolin-1(2H)-one
[Image: see text] Herein, we report practical Cu(BF(4))(2)/activated carbon-catalyzed amination of various anilines, isoquinolinone, and naphthyridinone with aryl boronic acids. The ultrasonic and rotary evaporation treatment of the mixture of aq. Cu(BF(4))(2) and activated carbon in methanol afford...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773803/ https://www.ncbi.nlm.nih.gov/pubmed/36570313 http://dx.doi.org/10.1021/acsomega.2c04299 |
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author | Wu, Shuang Liu, Qiong Zhang, Quanfeng Zhou, Ya Liu, Meiyan Zeng, Youlin |
author_facet | Wu, Shuang Liu, Qiong Zhang, Quanfeng Zhou, Ya Liu, Meiyan Zeng, Youlin |
author_sort | Wu, Shuang |
collection | PubMed |
description | [Image: see text] Herein, we report practical Cu(BF(4))(2)/activated carbon-catalyzed amination of various anilines, isoquinolinone, and naphthyridinone with aryl boronic acids. The ultrasonic and rotary evaporation treatment of the mixture of aq. Cu(BF(4))(2) and activated carbon in methanol afforded a novel Cu(II)-catalyst, which is air-stable and can be effectively applied in the Chan–Lam coupling reaction. The products of N-arylation were isolated in good to excellent yields at low catalytic loading. And Cu(BF(4))(2)/AC also showed good reusability. |
format | Online Article Text |
id | pubmed-9773803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97738032022-12-23 Cu(BF(4))(2)/AC-Catalyzed Synthesis of N-Substituted Anilines, N-Substituted 1,6-Naphthyridin-5(6H)-one, and Isoquinolin-1(2H)-one Wu, Shuang Liu, Qiong Zhang, Quanfeng Zhou, Ya Liu, Meiyan Zeng, Youlin ACS Omega [Image: see text] Herein, we report practical Cu(BF(4))(2)/activated carbon-catalyzed amination of various anilines, isoquinolinone, and naphthyridinone with aryl boronic acids. The ultrasonic and rotary evaporation treatment of the mixture of aq. Cu(BF(4))(2) and activated carbon in methanol afforded a novel Cu(II)-catalyst, which is air-stable and can be effectively applied in the Chan–Lam coupling reaction. The products of N-arylation were isolated in good to excellent yields at low catalytic loading. And Cu(BF(4))(2)/AC also showed good reusability. American Chemical Society 2022-12-07 /pmc/articles/PMC9773803/ /pubmed/36570313 http://dx.doi.org/10.1021/acsomega.2c04299 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Wu, Shuang Liu, Qiong Zhang, Quanfeng Zhou, Ya Liu, Meiyan Zeng, Youlin Cu(BF(4))(2)/AC-Catalyzed Synthesis of N-Substituted Anilines, N-Substituted 1,6-Naphthyridin-5(6H)-one, and Isoquinolin-1(2H)-one |
title | Cu(BF(4))(2)/AC-Catalyzed Synthesis
of N-Substituted Anilines, N-Substituted 1,6-Naphthyridin-5(6H)-one,
and Isoquinolin-1(2H)-one |
title_full | Cu(BF(4))(2)/AC-Catalyzed Synthesis
of N-Substituted Anilines, N-Substituted 1,6-Naphthyridin-5(6H)-one,
and Isoquinolin-1(2H)-one |
title_fullStr | Cu(BF(4))(2)/AC-Catalyzed Synthesis
of N-Substituted Anilines, N-Substituted 1,6-Naphthyridin-5(6H)-one,
and Isoquinolin-1(2H)-one |
title_full_unstemmed | Cu(BF(4))(2)/AC-Catalyzed Synthesis
of N-Substituted Anilines, N-Substituted 1,6-Naphthyridin-5(6H)-one,
and Isoquinolin-1(2H)-one |
title_short | Cu(BF(4))(2)/AC-Catalyzed Synthesis
of N-Substituted Anilines, N-Substituted 1,6-Naphthyridin-5(6H)-one,
and Isoquinolin-1(2H)-one |
title_sort | cu(bf(4))(2)/ac-catalyzed synthesis
of n-substituted anilines, n-substituted 1,6-naphthyridin-5(6h)-one,
and isoquinolin-1(2h)-one |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773803/ https://www.ncbi.nlm.nih.gov/pubmed/36570313 http://dx.doi.org/10.1021/acsomega.2c04299 |
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