Tunable Aryl Imidazolium Recyclable Ionic Liquid with Dual Brønsted–Lewis Acid as Green Catalyst for Friedel–Crafts Acylation and Thioesterification

Unique tunable aryl imidazolium ionic liquids successfully catalyzed Friedel–Crafts acylation and thioesterification in sealed tubes. These reactions can form a C−C bond and a C−S bond with high atom economy. Ionic liquids exhibited high activity and catalyzed essential reactions with good to excell...

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Autores principales: Lin, Yi-Jyun, Wu, Yao-Peng, Thul, Mayur, Hung, Ming-Wei, Chou, Shih-Huan, Chen, Wen-Tin, Lin, Wesley, Lin, Michelle, Reddy, Daggula Mallikarjuna, Wu, Hsin-Ru, Ho, Wen-Yueh, Luo, Shun-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024267/
https://www.ncbi.nlm.nih.gov/pubmed/31952217
http://dx.doi.org/10.3390/molecules25020352
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author Lin, Yi-Jyun
Wu, Yao-Peng
Thul, Mayur
Hung, Ming-Wei
Chou, Shih-Huan
Chen, Wen-Tin
Lin, Wesley
Lin, Michelle
Reddy, Daggula Mallikarjuna
Wu, Hsin-Ru
Ho, Wen-Yueh
Luo, Shun-Yuan
author_facet Lin, Yi-Jyun
Wu, Yao-Peng
Thul, Mayur
Hung, Ming-Wei
Chou, Shih-Huan
Chen, Wen-Tin
Lin, Wesley
Lin, Michelle
Reddy, Daggula Mallikarjuna
Wu, Hsin-Ru
Ho, Wen-Yueh
Luo, Shun-Yuan
author_sort Lin, Yi-Jyun
collection PubMed
description Unique tunable aryl imidazolium ionic liquids successfully catalyzed Friedel–Crafts acylation and thioesterification in sealed tubes. These reactions can form a C−C bond and a C−S bond with high atom economy. Ionic liquids exhibited high activity and catalyzed essential reactions with good to excellent yields while retaining their catalytic activities for recycling.
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spelling pubmed-70242672020-03-11 Tunable Aryl Imidazolium Recyclable Ionic Liquid with Dual Brønsted–Lewis Acid as Green Catalyst for Friedel–Crafts Acylation and Thioesterification Lin, Yi-Jyun Wu, Yao-Peng Thul, Mayur Hung, Ming-Wei Chou, Shih-Huan Chen, Wen-Tin Lin, Wesley Lin, Michelle Reddy, Daggula Mallikarjuna Wu, Hsin-Ru Ho, Wen-Yueh Luo, Shun-Yuan Molecules Article Unique tunable aryl imidazolium ionic liquids successfully catalyzed Friedel–Crafts acylation and thioesterification in sealed tubes. These reactions can form a C−C bond and a C−S bond with high atom economy. Ionic liquids exhibited high activity and catalyzed essential reactions with good to excellent yields while retaining their catalytic activities for recycling. MDPI 2020-01-15 /pmc/articles/PMC7024267/ /pubmed/31952217 http://dx.doi.org/10.3390/molecules25020352 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 Article
Lin, Yi-Jyun
Wu, Yao-Peng
Thul, Mayur
Hung, Ming-Wei
Chou, Shih-Huan
Chen, Wen-Tin
Lin, Wesley
Lin, Michelle
Reddy, Daggula Mallikarjuna
Wu, Hsin-Ru
Ho, Wen-Yueh
Luo, Shun-Yuan
Tunable Aryl Imidazolium Recyclable Ionic Liquid with Dual Brønsted–Lewis Acid as Green Catalyst for Friedel–Crafts Acylation and Thioesterification
title Tunable Aryl Imidazolium Recyclable Ionic Liquid with Dual Brønsted–Lewis Acid as Green Catalyst for Friedel–Crafts Acylation and Thioesterification
title_full Tunable Aryl Imidazolium Recyclable Ionic Liquid with Dual Brønsted–Lewis Acid as Green Catalyst for Friedel–Crafts Acylation and Thioesterification
title_fullStr Tunable Aryl Imidazolium Recyclable Ionic Liquid with Dual Brønsted–Lewis Acid as Green Catalyst for Friedel–Crafts Acylation and Thioesterification
title_full_unstemmed Tunable Aryl Imidazolium Recyclable Ionic Liquid with Dual Brønsted–Lewis Acid as Green Catalyst for Friedel–Crafts Acylation and Thioesterification
title_short Tunable Aryl Imidazolium Recyclable Ionic Liquid with Dual Brønsted–Lewis Acid as Green Catalyst for Friedel–Crafts Acylation and Thioesterification
title_sort tunable aryl imidazolium recyclable ionic liquid with dual brønsted–lewis acid as green catalyst for friedel–crafts acylation and thioesterification
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024267/
https://www.ncbi.nlm.nih.gov/pubmed/31952217
http://dx.doi.org/10.3390/molecules25020352
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