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...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Yi-Lun, Shi, Zhaojiang, Shen, Tao, Ye, Ke-Yin
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