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One-Pot Three-Component Coupling Reaction of α-Amino Aryl Ketones, Indoles, and Perbromomethane Under Mild Conditions

A simple and efficient one-pot three-component cascade reaction of α-amino aryl ketones, indoles, and CBr(4) in moderate to good yields has been developed. This new strategy exhibits excellent mild reaction conditions and step-economy, easily accessible reactants, and simultaneous construction of th...

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Autores principales: Chen, De, Lu, Hao, Liu, Yuxuan, Deng, Wei, Qiu, Renhua, Xiang, Jiannan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855049/
https://www.ncbi.nlm.nih.gov/pubmed/35186884
http://dx.doi.org/10.3389/fchem.2022.825772
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author Chen, De
Lu, Hao
Liu, Yuxuan
Deng, Wei
Qiu, Renhua
Xiang, Jiannan
author_facet Chen, De
Lu, Hao
Liu, Yuxuan
Deng, Wei
Qiu, Renhua
Xiang, Jiannan
author_sort Chen, De
collection PubMed
description A simple and efficient one-pot three-component cascade reaction of α-amino aryl ketones, indoles, and CBr(4) in moderate to good yields has been developed. This new strategy exhibits excellent mild reaction conditions and step-economy, easily accessible reactants, and simultaneous construction of three different new bonds (C=N, C–C, and N-Br) in a single step. It is worth noting that the protocol developed provides a simple and practical tool for the construction of diverse indole-containing heterocyclic frameworks, indicating its potential applications in medicinal and material chemistry.
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spelling pubmed-88550492022-02-19 One-Pot Three-Component Coupling Reaction of α-Amino Aryl Ketones, Indoles, and Perbromomethane Under Mild Conditions Chen, De Lu, Hao Liu, Yuxuan Deng, Wei Qiu, Renhua Xiang, Jiannan Front Chem Chemistry A simple and efficient one-pot three-component cascade reaction of α-amino aryl ketones, indoles, and CBr(4) in moderate to good yields has been developed. This new strategy exhibits excellent mild reaction conditions and step-economy, easily accessible reactants, and simultaneous construction of three different new bonds (C=N, C–C, and N-Br) in a single step. It is worth noting that the protocol developed provides a simple and practical tool for the construction of diverse indole-containing heterocyclic frameworks, indicating its potential applications in medicinal and material chemistry. Frontiers Media S.A. 2022-02-04 /pmc/articles/PMC8855049/ /pubmed/35186884 http://dx.doi.org/10.3389/fchem.2022.825772 Text en Copyright © 2022 Chen, Lu, Liu, Deng, Qiu and Xiang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Chen, De
Lu, Hao
Liu, Yuxuan
Deng, Wei
Qiu, Renhua
Xiang, Jiannan
One-Pot Three-Component Coupling Reaction of α-Amino Aryl Ketones, Indoles, and Perbromomethane Under Mild Conditions
title One-Pot Three-Component Coupling Reaction of α-Amino Aryl Ketones, Indoles, and Perbromomethane Under Mild Conditions
title_full One-Pot Three-Component Coupling Reaction of α-Amino Aryl Ketones, Indoles, and Perbromomethane Under Mild Conditions
title_fullStr One-Pot Three-Component Coupling Reaction of α-Amino Aryl Ketones, Indoles, and Perbromomethane Under Mild Conditions
title_full_unstemmed One-Pot Three-Component Coupling Reaction of α-Amino Aryl Ketones, Indoles, and Perbromomethane Under Mild Conditions
title_short One-Pot Three-Component Coupling Reaction of α-Amino Aryl Ketones, Indoles, and Perbromomethane Under Mild Conditions
title_sort one-pot three-component coupling reaction of α-amino aryl ketones, indoles, and perbromomethane under mild conditions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855049/
https://www.ncbi.nlm.nih.gov/pubmed/35186884
http://dx.doi.org/10.3389/fchem.2022.825772
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