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Metal-free and solvent-free synthesis of m-terphenyls through tandem cyclocondensation of aryl methyl ketones with triethyl orthoformate

Reported here is a novel cyclocondensation of aryl methyl ketones and triethyl orthoformate for the simple synthesis of m-terphenyls. In the presence of a catalytic amount of TfOH, alkyl- and chloro-substituted acetophenones produced a series of terphenyls through a tandem reaction which merged six...

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Autores principales: Xiao, Xiaoqin, Luo, Juan, Gan, Zongjie, Jiang, Wengao, Tang, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050746/
https://www.ncbi.nlm.nih.gov/pubmed/35496630
http://dx.doi.org/10.1039/d0ra00578a
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author Xiao, Xiaoqin
Luo, Juan
Gan, Zongjie
Jiang, Wengao
Tang, Qiang
author_facet Xiao, Xiaoqin
Luo, Juan
Gan, Zongjie
Jiang, Wengao
Tang, Qiang
author_sort Xiao, Xiaoqin
collection PubMed
description Reported here is a novel cyclocondensation of aryl methyl ketones and triethyl orthoformate for the simple synthesis of m-terphenyls. In the presence of a catalytic amount of TfOH, alkyl- and chloro-substituted acetophenones produced a series of terphenyls through a tandem reaction which merged six steps into a one-pot procedure. Moreover, the corresponding ester products were obtained when using other substituted acetophenones as the starting materials under the same reaction conditions.
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spelling pubmed-90507462022-04-29 Metal-free and solvent-free synthesis of m-terphenyls through tandem cyclocondensation of aryl methyl ketones with triethyl orthoformate Xiao, Xiaoqin Luo, Juan Gan, Zongjie Jiang, Wengao Tang, Qiang RSC Adv Chemistry Reported here is a novel cyclocondensation of aryl methyl ketones and triethyl orthoformate for the simple synthesis of m-terphenyls. In the presence of a catalytic amount of TfOH, alkyl- and chloro-substituted acetophenones produced a series of terphenyls through a tandem reaction which merged six steps into a one-pot procedure. Moreover, the corresponding ester products were obtained when using other substituted acetophenones as the starting materials under the same reaction conditions. The Royal Society of Chemistry 2020-03-25 /pmc/articles/PMC9050746/ /pubmed/35496630 http://dx.doi.org/10.1039/d0ra00578a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Xiao, Xiaoqin
Luo, Juan
Gan, Zongjie
Jiang, Wengao
Tang, Qiang
Metal-free and solvent-free synthesis of m-terphenyls through tandem cyclocondensation of aryl methyl ketones with triethyl orthoformate
title Metal-free and solvent-free synthesis of m-terphenyls through tandem cyclocondensation of aryl methyl ketones with triethyl orthoformate
title_full Metal-free and solvent-free synthesis of m-terphenyls through tandem cyclocondensation of aryl methyl ketones with triethyl orthoformate
title_fullStr Metal-free and solvent-free synthesis of m-terphenyls through tandem cyclocondensation of aryl methyl ketones with triethyl orthoformate
title_full_unstemmed Metal-free and solvent-free synthesis of m-terphenyls through tandem cyclocondensation of aryl methyl ketones with triethyl orthoformate
title_short Metal-free and solvent-free synthesis of m-terphenyls through tandem cyclocondensation of aryl methyl ketones with triethyl orthoformate
title_sort metal-free and solvent-free synthesis of m-terphenyls through tandem cyclocondensation of aryl methyl ketones with triethyl orthoformate
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050746/
https://www.ncbi.nlm.nih.gov/pubmed/35496630
http://dx.doi.org/10.1039/d0ra00578a
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