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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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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. |
format | Online Article Text |
id | pubmed-9049633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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