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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...

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Detalles Bibliográficos
Autores principales: Hirano, Koji, Miura, Masahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
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.
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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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