Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Hao, Feiyue, Nishiwaki, Nagatoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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
_version_ 1783500505402572800
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