Cargando…
An Efficient Metal-Free Oxidative Esterification and Amination of Benzyl C–H Bond
An esterification and amination of benzylic C–H bonds was developed by using 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) under metal- and iodide-free conditions. Both carboxylic acids and amines could be used as ideal coupling partners for the oxidative coupling reactions with various diarylmeth...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180972/ https://www.ncbi.nlm.nih.gov/pubmed/32230851 http://dx.doi.org/10.3390/molecules25071527 |
_version_ | 1783525945189072896 |
---|---|
author | Liu, Saiwen Chen, Ru He, Guowen Zhang, Jin |
author_facet | Liu, Saiwen Chen, Ru He, Guowen Zhang, Jin |
author_sort | Liu, Saiwen |
collection | PubMed |
description | An esterification and amination of benzylic C–H bonds was developed by using 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) under metal- and iodide-free conditions. Both carboxylic acids and amines could be used as ideal coupling partners for the oxidative coupling reactions with various diarylmethanes. A close to equal amount of coupling reagents was enough to afford the product in good to high yields. |
format | Online Article Text |
id | pubmed-7180972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71809722020-04-30 An Efficient Metal-Free Oxidative Esterification and Amination of Benzyl C–H Bond Liu, Saiwen Chen, Ru He, Guowen Zhang, Jin Molecules Communication An esterification and amination of benzylic C–H bonds was developed by using 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) under metal- and iodide-free conditions. Both carboxylic acids and amines could be used as ideal coupling partners for the oxidative coupling reactions with various diarylmethanes. A close to equal amount of coupling reagents was enough to afford the product in good to high yields. MDPI 2020-03-27 /pmc/articles/PMC7180972/ /pubmed/32230851 http://dx.doi.org/10.3390/molecules25071527 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Liu, Saiwen Chen, Ru He, Guowen Zhang, Jin An Efficient Metal-Free Oxidative Esterification and Amination of Benzyl C–H Bond |
title | An Efficient Metal-Free Oxidative Esterification and Amination of Benzyl C–H Bond |
title_full | An Efficient Metal-Free Oxidative Esterification and Amination of Benzyl C–H Bond |
title_fullStr | An Efficient Metal-Free Oxidative Esterification and Amination of Benzyl C–H Bond |
title_full_unstemmed | An Efficient Metal-Free Oxidative Esterification and Amination of Benzyl C–H Bond |
title_short | An Efficient Metal-Free Oxidative Esterification and Amination of Benzyl C–H Bond |
title_sort | efficient metal-free oxidative esterification and amination of benzyl c–h bond |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180972/ https://www.ncbi.nlm.nih.gov/pubmed/32230851 http://dx.doi.org/10.3390/molecules25071527 |
work_keys_str_mv | AT liusaiwen anefficientmetalfreeoxidativeesterificationandaminationofbenzylchbond AT chenru anefficientmetalfreeoxidativeesterificationandaminationofbenzylchbond AT heguowen anefficientmetalfreeoxidativeesterificationandaminationofbenzylchbond AT zhangjin anefficientmetalfreeoxidativeesterificationandaminationofbenzylchbond AT liusaiwen efficientmetalfreeoxidativeesterificationandaminationofbenzylchbond AT chenru efficientmetalfreeoxidativeesterificationandaminationofbenzylchbond AT heguowen efficientmetalfreeoxidativeesterificationandaminationofbenzylchbond AT zhangjin efficientmetalfreeoxidativeesterificationandaminationofbenzylchbond |