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Recent Progress in Nitro-Promoted Direct Functionalization of Pyridones and Quinolones
Nitro group is one of the most important functional groups in organic syntheses because its strongly electron-withdrawing ability activates the scaffold, facilitating the reaction with nucleophilic reagents or the Diels–Alder reaction. In this review, recent progress in the nitro-promoted direct fun...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037792/ https://www.ncbi.nlm.nih.gov/pubmed/32033284 http://dx.doi.org/10.3390/molecules25030673 |
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author | Hao, Feiyue Nishiwaki, Nagatoshi |
author_facet | Hao, Feiyue Nishiwaki, Nagatoshi |
author_sort | Hao, Feiyue |
collection | PubMed |
description | Nitro group is one of the most important functional groups in organic syntheses because its strongly electron-withdrawing ability activates the scaffold, facilitating the reaction with nucleophilic reagents or the Diels–Alder reaction. In this review, recent progress in the nitro-promoted direct functionalization of pyridones and quinolones is highlighted to complement previous reviews. |
format | Online Article Text |
id | pubmed-7037792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70377922020-03-10 Recent Progress in Nitro-Promoted Direct Functionalization of Pyridones and Quinolones Hao, Feiyue Nishiwaki, Nagatoshi Molecules Review Nitro group is one of the most important functional groups in organic syntheses because its strongly electron-withdrawing ability activates the scaffold, facilitating the reaction with nucleophilic reagents or the Diels–Alder reaction. In this review, recent progress in the nitro-promoted direct functionalization of pyridones and quinolones is highlighted to complement previous reviews. MDPI 2020-02-05 /pmc/articles/PMC7037792/ /pubmed/32033284 http://dx.doi.org/10.3390/molecules25030673 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Hao, Feiyue Nishiwaki, Nagatoshi Recent Progress in Nitro-Promoted Direct Functionalization of Pyridones and Quinolones |
title | Recent Progress in Nitro-Promoted Direct Functionalization of Pyridones and Quinolones |
title_full | Recent Progress in Nitro-Promoted Direct Functionalization of Pyridones and Quinolones |
title_fullStr | Recent Progress in Nitro-Promoted Direct Functionalization of Pyridones and Quinolones |
title_full_unstemmed | Recent Progress in Nitro-Promoted Direct Functionalization of Pyridones and Quinolones |
title_short | Recent Progress in Nitro-Promoted Direct Functionalization of Pyridones and Quinolones |
title_sort | recent progress in nitro-promoted direct functionalization of pyridones and quinolones |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037792/ https://www.ncbi.nlm.nih.gov/pubmed/32033284 http://dx.doi.org/10.3390/molecules25030673 |
work_keys_str_mv | AT haofeiyue recentprogressinnitropromoteddirectfunctionalizationofpyridonesandquinolones AT nishiwakinagatoshi recentprogressinnitropromoteddirectfunctionalizationofpyridonesandquinolones |