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Ru(ii)-catalyzed C6-selective C–H acylmethylation of pyridones using sulfoxonium ylides as carbene precursors

In this study, we describe a method using sulfoxonium ylides as carbene precursors to achieve C6-selective acylmethylation of pyridones catalyzed by a ruthenium(ii) complex. This approach featured mild reaction conditions, moderate to excellent yields, high step economy, and had excellent functional...

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Detalles Bibliográficos
Autores principales: Fu, Yangjie, Wang, Zhaohui, Zhang, Qiyu, Li, Zhiyu, Liu, Hong, Bi, Xiaoling, Wang, Jiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049633/
https://www.ncbi.nlm.nih.gov/pubmed/35496007
http://dx.doi.org/10.1039/c9ra10749e
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author Fu, Yangjie
Wang, Zhaohui
Zhang, Qiyu
Li, Zhiyu
Liu, Hong
Bi, Xiaoling
Wang, Jiang
author_facet Fu, Yangjie
Wang, Zhaohui
Zhang, Qiyu
Li, Zhiyu
Liu, Hong
Bi, Xiaoling
Wang, Jiang
author_sort Fu, Yangjie
collection PubMed
description In this study, we describe a method using sulfoxonium ylides as carbene precursors to achieve C6-selective acylmethylation of pyridones catalyzed by a ruthenium(ii) complex. This approach featured mild reaction conditions, moderate to excellent yields, high step economy, and had excellent functional group tolerance with good site selectivity. Besides, gram-scale preparation, synthetic utility, and mechanistic studies were conducted. It offers a direct and efficient way to synthesize pyridone derivatives.
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spelling pubmed-90496332022-04-29 Ru(ii)-catalyzed C6-selective C–H acylmethylation of pyridones using sulfoxonium ylides as carbene precursors Fu, Yangjie Wang, Zhaohui Zhang, Qiyu Li, Zhiyu Liu, Hong Bi, Xiaoling Wang, Jiang RSC Adv Chemistry In this study, we describe a method using sulfoxonium ylides as carbene precursors to achieve C6-selective acylmethylation of pyridones catalyzed by a ruthenium(ii) complex. This approach featured mild reaction conditions, moderate to excellent yields, high step economy, and had excellent functional group tolerance with good site selectivity. Besides, gram-scale preparation, synthetic utility, and mechanistic studies were conducted. It offers a direct and efficient way to synthesize pyridone derivatives. The Royal Society of Chemistry 2020-02-11 /pmc/articles/PMC9049633/ /pubmed/35496007 http://dx.doi.org/10.1039/c9ra10749e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Fu, Yangjie
Wang, Zhaohui
Zhang, Qiyu
Li, Zhiyu
Liu, Hong
Bi, Xiaoling
Wang, Jiang
Ru(ii)-catalyzed C6-selective C–H acylmethylation of pyridones using sulfoxonium ylides as carbene precursors
title Ru(ii)-catalyzed C6-selective C–H acylmethylation of pyridones using sulfoxonium ylides as carbene precursors
title_full Ru(ii)-catalyzed C6-selective C–H acylmethylation of pyridones using sulfoxonium ylides as carbene precursors
title_fullStr Ru(ii)-catalyzed C6-selective C–H acylmethylation of pyridones using sulfoxonium ylides as carbene precursors
title_full_unstemmed Ru(ii)-catalyzed C6-selective C–H acylmethylation of pyridones using sulfoxonium ylides as carbene precursors
title_short Ru(ii)-catalyzed C6-selective C–H acylmethylation of pyridones using sulfoxonium ylides as carbene precursors
title_sort ru(ii)-catalyzed c6-selective c–h acylmethylation of pyridones using sulfoxonium ylides as carbene precursors
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049633/
https://www.ncbi.nlm.nih.gov/pubmed/35496007
http://dx.doi.org/10.1039/c9ra10749e
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