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External Catalyst- and Additive-Free Photo-Oxidation of Aromatic Alcohols to Carboxylic Acids or Ketones Using Air/O(2)
We present an environment-friendly and highly efficient method for the oxidation of aromatic alcohols to carboxylic acids or ketones in air via light irradiation under external catalyst-, additive-, and base-free conditions. The photoreaction system exhibits a wide substrate scope and the potential...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10096038/ https://www.ncbi.nlm.nih.gov/pubmed/37049794 http://dx.doi.org/10.3390/molecules28073031 |
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author | Xu, Meng Ou, Jinhua Luo, Kejun Liang, Rongtao Liu, Jian Li, Ni Hu, Bonian Liu, Kaijian |
author_facet | Xu, Meng Ou, Jinhua Luo, Kejun Liang, Rongtao Liu, Jian Li, Ni Hu, Bonian Liu, Kaijian |
author_sort | Xu, Meng |
collection | PubMed |
description | We present an environment-friendly and highly efficient method for the oxidation of aromatic alcohols to carboxylic acids or ketones in air via light irradiation under external catalyst-, additive-, and base-free conditions. The photoreaction system exhibits a wide substrate scope and the potential for large-scale applications. Most of the desired products are easily obtained via recrystallization and separation from low-boiling reaction medium acetone in good yields, and the products can be subsequent directly transformed without further purification. |
format | Online Article Text |
id | pubmed-10096038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100960382023-04-13 External Catalyst- and Additive-Free Photo-Oxidation of Aromatic Alcohols to Carboxylic Acids or Ketones Using Air/O(2) Xu, Meng Ou, Jinhua Luo, Kejun Liang, Rongtao Liu, Jian Li, Ni Hu, Bonian Liu, Kaijian Molecules Article We present an environment-friendly and highly efficient method for the oxidation of aromatic alcohols to carboxylic acids or ketones in air via light irradiation under external catalyst-, additive-, and base-free conditions. The photoreaction system exhibits a wide substrate scope and the potential for large-scale applications. Most of the desired products are easily obtained via recrystallization and separation from low-boiling reaction medium acetone in good yields, and the products can be subsequent directly transformed without further purification. MDPI 2023-03-28 /pmc/articles/PMC10096038/ /pubmed/37049794 http://dx.doi.org/10.3390/molecules28073031 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Xu, Meng Ou, Jinhua Luo, Kejun Liang, Rongtao Liu, Jian Li, Ni Hu, Bonian Liu, Kaijian External Catalyst- and Additive-Free Photo-Oxidation of Aromatic Alcohols to Carboxylic Acids or Ketones Using Air/O(2) |
title | External Catalyst- and Additive-Free Photo-Oxidation of Aromatic Alcohols to Carboxylic Acids or Ketones Using Air/O(2) |
title_full | External Catalyst- and Additive-Free Photo-Oxidation of Aromatic Alcohols to Carboxylic Acids or Ketones Using Air/O(2) |
title_fullStr | External Catalyst- and Additive-Free Photo-Oxidation of Aromatic Alcohols to Carboxylic Acids or Ketones Using Air/O(2) |
title_full_unstemmed | External Catalyst- and Additive-Free Photo-Oxidation of Aromatic Alcohols to Carboxylic Acids or Ketones Using Air/O(2) |
title_short | External Catalyst- and Additive-Free Photo-Oxidation of Aromatic Alcohols to Carboxylic Acids or Ketones Using Air/O(2) |
title_sort | external catalyst- and additive-free photo-oxidation of aromatic alcohols to carboxylic acids or ketones using air/o(2) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10096038/ https://www.ncbi.nlm.nih.gov/pubmed/37049794 http://dx.doi.org/10.3390/molecules28073031 |
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