Facile synthesis of O-acylhydroxamates via reaction of oxime chlorides with carboxylic acids

A simple and efficient method for the synthesis of O-acylhydroxamate derivatives from oxime chlorides and carboxylic acids was developed. The reaction affords clean and facile access to diverse O-acylhydroxamates in high yields (up to 85%). The chemical structure of a typical product was confirmed u...

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Autores principales: Wang, Kai-Kai, Li, Yan-Li, Zhao, Ying-Chao, Zhang, Shan-Shan, Chen, Rongxiang, Sun, Aili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044751/
https://www.ncbi.nlm.nih.gov/pubmed/35494140
http://dx.doi.org/10.1039/d1ra06860a
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author Wang, Kai-Kai
Li, Yan-Li
Zhao, Ying-Chao
Zhang, Shan-Shan
Chen, Rongxiang
Sun, Aili
author_facet Wang, Kai-Kai
Li, Yan-Li
Zhao, Ying-Chao
Zhang, Shan-Shan
Chen, Rongxiang
Sun, Aili
author_sort Wang, Kai-Kai
collection PubMed
description A simple and efficient method for the synthesis of O-acylhydroxamate derivatives from oxime chlorides and carboxylic acids was developed. The reaction affords clean and facile access to diverse O-acylhydroxamates in high yields (up to 85%). The chemical structure of a typical product was confirmed using single-crystal X-ray structure analysis.
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spelling pubmed-90447512022-04-28 Facile synthesis of O-acylhydroxamates via reaction of oxime chlorides with carboxylic acids Wang, Kai-Kai Li, Yan-Li Zhao, Ying-Chao Zhang, Shan-Shan Chen, Rongxiang Sun, Aili RSC Adv Chemistry A simple and efficient method for the synthesis of O-acylhydroxamate derivatives from oxime chlorides and carboxylic acids was developed. The reaction affords clean and facile access to diverse O-acylhydroxamates in high yields (up to 85%). The chemical structure of a typical product was confirmed using single-crystal X-ray structure analysis. The Royal Society of Chemistry 2021-12-20 /pmc/articles/PMC9044751/ /pubmed/35494140 http://dx.doi.org/10.1039/d1ra06860a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wang, Kai-Kai
Li, Yan-Li
Zhao, Ying-Chao
Zhang, Shan-Shan
Chen, Rongxiang
Sun, Aili
Facile synthesis of O-acylhydroxamates via reaction of oxime chlorides with carboxylic acids
title Facile synthesis of O-acylhydroxamates via reaction of oxime chlorides with carboxylic acids
title_full Facile synthesis of O-acylhydroxamates via reaction of oxime chlorides with carboxylic acids
title_fullStr Facile synthesis of O-acylhydroxamates via reaction of oxime chlorides with carboxylic acids
title_full_unstemmed Facile synthesis of O-acylhydroxamates via reaction of oxime chlorides with carboxylic acids
title_short Facile synthesis of O-acylhydroxamates via reaction of oxime chlorides with carboxylic acids
title_sort facile synthesis of o-acylhydroxamates via reaction of oxime chlorides with carboxylic acids
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044751/
https://www.ncbi.nlm.nih.gov/pubmed/35494140
http://dx.doi.org/10.1039/d1ra06860a
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