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Electrosynthesis of Quinazolines and Quinazolinones via an Anodic Direct Oxidation C(sp(3))-H Amination/C-N Cleavage of Tertiary Amine in Aqueous Medium
[Image: see text] An electrochemical synthesis for quinazolines and quinazolinones was developed via a C(sp(3))-H amination/C-N cleavage by virtue of the anodic oxidation. The reaction can be carried out in aqueous media under mild conditions to afford the desired products with high yields. The reac...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745442/ https://www.ncbi.nlm.nih.gov/pubmed/33344851 http://dx.doi.org/10.1021/acsomega.0c04865 |
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author | Zhou, Zhenghong Hu, Kangfei Wang, Jiawei Li, Zhibin Zhang, Yan Zha, Zhenggen Wang, Zhiyong |
author_facet | Zhou, Zhenghong Hu, Kangfei Wang, Jiawei Li, Zhibin Zhang, Yan Zha, Zhenggen Wang, Zhiyong |
author_sort | Zhou, Zhenghong |
collection | PubMed |
description | [Image: see text] An electrochemical synthesis for quinazolines and quinazolinones was developed via a C(sp(3))-H amination/C-N cleavage by virtue of the anodic oxidation. The reaction can be carried out in aqueous media under mild conditions to afford the desired products with high yields. The reaction mechanism was proposed after detailed investigation. |
format | Online Article Text |
id | pubmed-7745442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-77454422020-12-18 Electrosynthesis of Quinazolines and Quinazolinones via an Anodic Direct Oxidation C(sp(3))-H Amination/C-N Cleavage of Tertiary Amine in Aqueous Medium Zhou, Zhenghong Hu, Kangfei Wang, Jiawei Li, Zhibin Zhang, Yan Zha, Zhenggen Wang, Zhiyong ACS Omega [Image: see text] An electrochemical synthesis for quinazolines and quinazolinones was developed via a C(sp(3))-H amination/C-N cleavage by virtue of the anodic oxidation. The reaction can be carried out in aqueous media under mild conditions to afford the desired products with high yields. The reaction mechanism was proposed after detailed investigation. American Chemical Society 2020-12-01 /pmc/articles/PMC7745442/ /pubmed/33344851 http://dx.doi.org/10.1021/acsomega.0c04865 Text en © 2020 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Zhou, Zhenghong Hu, Kangfei Wang, Jiawei Li, Zhibin Zhang, Yan Zha, Zhenggen Wang, Zhiyong Electrosynthesis of Quinazolines and Quinazolinones via an Anodic Direct Oxidation C(sp(3))-H Amination/C-N Cleavage of Tertiary Amine in Aqueous Medium |
title | Electrosynthesis of Quinazolines and Quinazolinones
via an Anodic Direct Oxidation C(sp(3))-H Amination/C-N
Cleavage of Tertiary Amine in Aqueous Medium |
title_full | Electrosynthesis of Quinazolines and Quinazolinones
via an Anodic Direct Oxidation C(sp(3))-H Amination/C-N
Cleavage of Tertiary Amine in Aqueous Medium |
title_fullStr | Electrosynthesis of Quinazolines and Quinazolinones
via an Anodic Direct Oxidation C(sp(3))-H Amination/C-N
Cleavage of Tertiary Amine in Aqueous Medium |
title_full_unstemmed | Electrosynthesis of Quinazolines and Quinazolinones
via an Anodic Direct Oxidation C(sp(3))-H Amination/C-N
Cleavage of Tertiary Amine in Aqueous Medium |
title_short | Electrosynthesis of Quinazolines and Quinazolinones
via an Anodic Direct Oxidation C(sp(3))-H Amination/C-N
Cleavage of Tertiary Amine in Aqueous Medium |
title_sort | electrosynthesis of quinazolines and quinazolinones
via an anodic direct oxidation c(sp(3))-h amination/c-n
cleavage of tertiary amine in aqueous medium |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745442/ https://www.ncbi.nlm.nih.gov/pubmed/33344851 http://dx.doi.org/10.1021/acsomega.0c04865 |
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