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Heteropolyacid ionic liquid heterogeneously catalyzed synthesis of isochromans via oxa-Pictet–Spengler cyclization in dimethyl carbonate
A recyclable and efficient heterogeneous, green catalyst based on the synthesis of Keggin-type polyoxometalate (H(3)PMo(12)O(40)) and vitamin B1 analogue 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazol-3-ium (HEMT), i.e., [HEMTH]H(2)[PMo(12)O(40)] was prepared. Oxa-Pictet–Spengler cyclization of aryletha...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695662/ https://www.ncbi.nlm.nih.gov/pubmed/35423595 http://dx.doi.org/10.1039/d1ra01004b |
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author | Yang, Guoping Li, Ke Zeng, Kai Li, Yijin Yu, Tao Liu, Yufeng |
author_facet | Yang, Guoping Li, Ke Zeng, Kai Li, Yijin Yu, Tao Liu, Yufeng |
author_sort | Yang, Guoping |
collection | PubMed |
description | A recyclable and efficient heterogeneous, green catalyst based on the synthesis of Keggin-type polyoxometalate (H(3)PMo(12)O(40)) and vitamin B1 analogue 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazol-3-ium (HEMT), i.e., [HEMTH]H(2)[PMo(12)O(40)] was prepared. Oxa-Pictet–Spengler cyclization of arylethanols and aldehydes were catalyzed to afford various substituted isochromans in moderate conditions with excellent yields using dimethyl carbonate (DMC) as a green solvent. Furthermore, this protocol was applicable in a gram-scale reaction, and the catalyst could be recycled eight times without significant loss of activity. |
format | Online Article Text |
id | pubmed-8695662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86956622022-04-13 Heteropolyacid ionic liquid heterogeneously catalyzed synthesis of isochromans via oxa-Pictet–Spengler cyclization in dimethyl carbonate Yang, Guoping Li, Ke Zeng, Kai Li, Yijin Yu, Tao Liu, Yufeng RSC Adv Chemistry A recyclable and efficient heterogeneous, green catalyst based on the synthesis of Keggin-type polyoxometalate (H(3)PMo(12)O(40)) and vitamin B1 analogue 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazol-3-ium (HEMT), i.e., [HEMTH]H(2)[PMo(12)O(40)] was prepared. Oxa-Pictet–Spengler cyclization of arylethanols and aldehydes were catalyzed to afford various substituted isochromans in moderate conditions with excellent yields using dimethyl carbonate (DMC) as a green solvent. Furthermore, this protocol was applicable in a gram-scale reaction, and the catalyst could be recycled eight times without significant loss of activity. The Royal Society of Chemistry 2021-03-11 /pmc/articles/PMC8695662/ /pubmed/35423595 http://dx.doi.org/10.1039/d1ra01004b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Yang, Guoping Li, Ke Zeng, Kai Li, Yijin Yu, Tao Liu, Yufeng Heteropolyacid ionic liquid heterogeneously catalyzed synthesis of isochromans via oxa-Pictet–Spengler cyclization in dimethyl carbonate |
title | Heteropolyacid ionic liquid heterogeneously catalyzed synthesis of isochromans via oxa-Pictet–Spengler cyclization in dimethyl carbonate |
title_full | Heteropolyacid ionic liquid heterogeneously catalyzed synthesis of isochromans via oxa-Pictet–Spengler cyclization in dimethyl carbonate |
title_fullStr | Heteropolyacid ionic liquid heterogeneously catalyzed synthesis of isochromans via oxa-Pictet–Spengler cyclization in dimethyl carbonate |
title_full_unstemmed | Heteropolyacid ionic liquid heterogeneously catalyzed synthesis of isochromans via oxa-Pictet–Spengler cyclization in dimethyl carbonate |
title_short | Heteropolyacid ionic liquid heterogeneously catalyzed synthesis of isochromans via oxa-Pictet–Spengler cyclization in dimethyl carbonate |
title_sort | heteropolyacid ionic liquid heterogeneously catalyzed synthesis of isochromans via oxa-pictet–spengler cyclization in dimethyl carbonate |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695662/ https://www.ncbi.nlm.nih.gov/pubmed/35423595 http://dx.doi.org/10.1039/d1ra01004b |
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