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A lesson for site-selective C–H functionalization on 2-pyridones: radical, organometallic, directing group and steric controls
A 2-pyridone ring is a frequently occurring subunit in natural products, biologically active compounds, and pharmaceutical targets. Thus, the selective synthesis of substituted 2-pyridone derivatives through decoration and/or formation of pyridone rings has been one of the important longstanding sub...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875088/ https://www.ncbi.nlm.nih.gov/pubmed/29629070 http://dx.doi.org/10.1039/c7sc04509c |
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author | Hirano, Koji Miura, Masahiro |
author_facet | Hirano, Koji Miura, Masahiro |
author_sort | Hirano, Koji |
collection | PubMed |
description | A 2-pyridone ring is a frequently occurring subunit in natural products, biologically active compounds, and pharmaceutical targets. Thus, the selective synthesis of substituted 2-pyridone derivatives through decoration and/or formation of pyridone rings has been one of the important longstanding subjects in organic synthetic chemistry. This minireview focuses on recent advances in site-selective C–H functionalization on 2-pyridone. The reported procedures are categorized according to the site selectivity that is achieved, and the substrate scope, limitations, mechanism, and controlling factors are briefly summarized. |
format | Online Article Text |
id | pubmed-5875088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-58750882018-04-06 A lesson for site-selective C–H functionalization on 2-pyridones: radical, organometallic, directing group and steric controls Hirano, Koji Miura, Masahiro Chem Sci Chemistry A 2-pyridone ring is a frequently occurring subunit in natural products, biologically active compounds, and pharmaceutical targets. Thus, the selective synthesis of substituted 2-pyridone derivatives through decoration and/or formation of pyridone rings has been one of the important longstanding subjects in organic synthetic chemistry. This minireview focuses on recent advances in site-selective C–H functionalization on 2-pyridone. The reported procedures are categorized according to the site selectivity that is achieved, and the substrate scope, limitations, mechanism, and controlling factors are briefly summarized. Royal Society of Chemistry 2017-11-27 /pmc/articles/PMC5875088/ /pubmed/29629070 http://dx.doi.org/10.1039/c7sc04509c Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Hirano, Koji Miura, Masahiro A lesson for site-selective C–H functionalization on 2-pyridones: radical, organometallic, directing group and steric controls |
title | A lesson for site-selective C–H functionalization on 2-pyridones: radical, organometallic, directing group and steric controls |
title_full | A lesson for site-selective C–H functionalization on 2-pyridones: radical, organometallic, directing group and steric controls |
title_fullStr | A lesson for site-selective C–H functionalization on 2-pyridones: radical, organometallic, directing group and steric controls |
title_full_unstemmed | A lesson for site-selective C–H functionalization on 2-pyridones: radical, organometallic, directing group and steric controls |
title_short | A lesson for site-selective C–H functionalization on 2-pyridones: radical, organometallic, directing group and steric controls |
title_sort | lesson for site-selective c–h functionalization on 2-pyridones: radical, organometallic, directing group and steric controls |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875088/ https://www.ncbi.nlm.nih.gov/pubmed/29629070 http://dx.doi.org/10.1039/c7sc04509c |
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