Microwave-assisted green synthesis of anilines, phenols, and benzenediamines without transition metals, ligands, or organic solvents

A novel, microwave-assisted method producing anilines and phenols from activated aryl halides is reported. This high-yielding method reduces current reaction requirements and removes organic solvents and catalysts making a more efficient and eco-friendly alternative for the synthesis of important ph...

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Detalles Bibliográficos
Autores principales: McConnell, N., Frett, B., Li, H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6457683/
https://www.ncbi.nlm.nih.gov/pubmed/30984284
http://dx.doi.org/10.1080/17518253.2018.1486464
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author McConnell, N.
Frett, B.
Li, H.
author_facet McConnell, N.
Frett, B.
Li, H.
author_sort McConnell, N.
collection PubMed
description A novel, microwave-assisted method producing anilines and phenols from activated aryl halides is reported. This high-yielding method reduces current reaction requirements and removes organic solvents and catalysts making a more efficient and eco-friendly alternative for the synthesis of important pharmaceutical building blocks. [Image: see text]
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spelling pubmed-64576832019-05-03 Microwave-assisted green synthesis of anilines, phenols, and benzenediamines without transition metals, ligands, or organic solvents McConnell, N. Frett, B. Li, H. Green Chem Lett Rev Article A novel, microwave-assisted method producing anilines and phenols from activated aryl halides is reported. This high-yielding method reduces current reaction requirements and removes organic solvents and catalysts making a more efficient and eco-friendly alternative for the synthesis of important pharmaceutical building blocks. [Image: see text] 2018-07-03 2018 /pmc/articles/PMC6457683/ /pubmed/30984284 http://dx.doi.org/10.1080/17518253.2018.1486464 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
McConnell, N.
Frett, B.
Li, H.
Microwave-assisted green synthesis of anilines, phenols, and benzenediamines without transition metals, ligands, or organic solvents
title Microwave-assisted green synthesis of anilines, phenols, and benzenediamines without transition metals, ligands, or organic solvents
title_full Microwave-assisted green synthesis of anilines, phenols, and benzenediamines without transition metals, ligands, or organic solvents
title_fullStr Microwave-assisted green synthesis of anilines, phenols, and benzenediamines without transition metals, ligands, or organic solvents
title_full_unstemmed Microwave-assisted green synthesis of anilines, phenols, and benzenediamines without transition metals, ligands, or organic solvents
title_short Microwave-assisted green synthesis of anilines, phenols, and benzenediamines without transition metals, ligands, or organic solvents
title_sort microwave-assisted green synthesis of anilines, phenols, and benzenediamines without transition metals, ligands, or organic solvents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6457683/
https://www.ncbi.nlm.nih.gov/pubmed/30984284
http://dx.doi.org/10.1080/17518253.2018.1486464
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AT lih microwaveassistedgreensynthesisofanilinesphenolsandbenzenediamineswithouttransitionmetalsligandsororganicsolvents

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