Cargando…
Electrochemical vicinal oxyazidation of α-arylvinyl acetates
α-Azidoketones are valuable and versatile building blocks in the synthesis of various bioactive small molecules. Herein, we describe an environmentally friendly and efficient electrochemical vicinal oxyazidation protocol of α-arylvinyl acetates to afford diverse α-azidoketones in good yields without...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9379640/ https://www.ncbi.nlm.nih.gov/pubmed/36051561 http://dx.doi.org/10.3762/bjoc.18.103 |
_version_ | 1784768712501362688 |
---|---|
author | Li, Yi-Lun Shi, Zhaojiang Shen, Tao Ye, Ke-Yin |
author_facet | Li, Yi-Lun Shi, Zhaojiang Shen, Tao Ye, Ke-Yin |
author_sort | Li, Yi-Lun |
collection | PubMed |
description | α-Azidoketones are valuable and versatile building blocks in the synthesis of various bioactive small molecules. Herein, we describe an environmentally friendly and efficient electrochemical vicinal oxyazidation protocol of α-arylvinyl acetates to afford diverse α-azidoketones in good yields without the use of a stoichiometric amount of chemical oxidant. A range of functionality is shown to be compatible with this transformation, and further applications are demonstrated. |
format | Online Article Text |
id | pubmed-9379640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-93796402022-08-31 Electrochemical vicinal oxyazidation of α-arylvinyl acetates Li, Yi-Lun Shi, Zhaojiang Shen, Tao Ye, Ke-Yin Beilstein J Org Chem Letter α-Azidoketones are valuable and versatile building blocks in the synthesis of various bioactive small molecules. Herein, we describe an environmentally friendly and efficient electrochemical vicinal oxyazidation protocol of α-arylvinyl acetates to afford diverse α-azidoketones in good yields without the use of a stoichiometric amount of chemical oxidant. A range of functionality is shown to be compatible with this transformation, and further applications are demonstrated. Beilstein-Institut 2022-08-12 /pmc/articles/PMC9379640/ /pubmed/36051561 http://dx.doi.org/10.3762/bjoc.18.103 Text en Copyright © 2022, Li et al. https://creativecommons.org/licenses/by/4.0/This is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material. |
spellingShingle | Letter Li, Yi-Lun Shi, Zhaojiang Shen, Tao Ye, Ke-Yin Electrochemical vicinal oxyazidation of α-arylvinyl acetates |
title | Electrochemical vicinal oxyazidation of α-arylvinyl acetates |
title_full | Electrochemical vicinal oxyazidation of α-arylvinyl acetates |
title_fullStr | Electrochemical vicinal oxyazidation of α-arylvinyl acetates |
title_full_unstemmed | Electrochemical vicinal oxyazidation of α-arylvinyl acetates |
title_short | Electrochemical vicinal oxyazidation of α-arylvinyl acetates |
title_sort | electrochemical vicinal oxyazidation of α-arylvinyl acetates |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9379640/ https://www.ncbi.nlm.nih.gov/pubmed/36051561 http://dx.doi.org/10.3762/bjoc.18.103 |
work_keys_str_mv | AT liyilun electrochemicalvicinaloxyazidationofaarylvinylacetates AT shizhaojiang electrochemicalvicinaloxyazidationofaarylvinylacetates AT shentao electrochemicalvicinaloxyazidationofaarylvinylacetates AT yekeyin electrochemicalvicinaloxyazidationofaarylvinylacetates |