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Bifunctional phase-transfer catalysts for synthesis of 2-oxazolidinones from isocyanates and epoxides
A series of bifunctional phase-transfer catalysts (PTCs) were synthesized to catalyze the [3 + 2] coupling reaction of isocyanates and epoxides to afford 2-oxazolidinones in good to high yields (up to 92% yield) using PhCl as a solvent at 100 °C within 12 h. These bifunctional PTCs were easily prepa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050849/ https://www.ncbi.nlm.nih.gov/pubmed/35497599 http://dx.doi.org/10.1039/d0ra00693a |
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author | Cui, Dong-Xiao Li, Yue-Dan Huang, Ping Tian, Zhuang Jia, Yan-Yan Wang, Ping-An |
author_facet | Cui, Dong-Xiao Li, Yue-Dan Huang, Ping Tian, Zhuang Jia, Yan-Yan Wang, Ping-An |
author_sort | Cui, Dong-Xiao |
collection | PubMed |
description | A series of bifunctional phase-transfer catalysts (PTCs) were synthesized to catalyze the [3 + 2] coupling reaction of isocyanates and epoxides to afford 2-oxazolidinones in good to high yields (up to 92% yield) using PhCl as a solvent at 100 °C within 12 h. These bifunctional PTCs were easily prepared from commercially available tertiary-primary diamines and isocyanates (or isothiocyanates, mono-squaramides, respectively) in two simple steps with good modularity and demonstrated high efficiency (2.5 mol% catalyst-loading). The synergistic interaction of the quaternary ammonium salt center and hydrogen-bond donor group in the catalyst with the substrate is crucial to this atom-economic reaction. |
format | Online Article Text |
id | pubmed-9050849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90508492022-04-29 Bifunctional phase-transfer catalysts for synthesis of 2-oxazolidinones from isocyanates and epoxides Cui, Dong-Xiao Li, Yue-Dan Huang, Ping Tian, Zhuang Jia, Yan-Yan Wang, Ping-An RSC Adv Chemistry A series of bifunctional phase-transfer catalysts (PTCs) were synthesized to catalyze the [3 + 2] coupling reaction of isocyanates and epoxides to afford 2-oxazolidinones in good to high yields (up to 92% yield) using PhCl as a solvent at 100 °C within 12 h. These bifunctional PTCs were easily prepared from commercially available tertiary-primary diamines and isocyanates (or isothiocyanates, mono-squaramides, respectively) in two simple steps with good modularity and demonstrated high efficiency (2.5 mol% catalyst-loading). The synergistic interaction of the quaternary ammonium salt center and hydrogen-bond donor group in the catalyst with the substrate is crucial to this atom-economic reaction. The Royal Society of Chemistry 2020-03-26 /pmc/articles/PMC9050849/ /pubmed/35497599 http://dx.doi.org/10.1039/d0ra00693a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Cui, Dong-Xiao Li, Yue-Dan Huang, Ping Tian, Zhuang Jia, Yan-Yan Wang, Ping-An Bifunctional phase-transfer catalysts for synthesis of 2-oxazolidinones from isocyanates and epoxides |
title | Bifunctional phase-transfer catalysts for synthesis of 2-oxazolidinones from isocyanates and epoxides |
title_full | Bifunctional phase-transfer catalysts for synthesis of 2-oxazolidinones from isocyanates and epoxides |
title_fullStr | Bifunctional phase-transfer catalysts for synthesis of 2-oxazolidinones from isocyanates and epoxides |
title_full_unstemmed | Bifunctional phase-transfer catalysts for synthesis of 2-oxazolidinones from isocyanates and epoxides |
title_short | Bifunctional phase-transfer catalysts for synthesis of 2-oxazolidinones from isocyanates and epoxides |
title_sort | bifunctional phase-transfer catalysts for synthesis of 2-oxazolidinones from isocyanates and epoxides |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050849/ https://www.ncbi.nlm.nih.gov/pubmed/35497599 http://dx.doi.org/10.1039/d0ra00693a |
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