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Direct Dehydrative Glycosylation Catalyzed by Diphenylammonium Triflate
Methods for direct dehydrative glycosylations of carbohydrate hemiacetals catalyzed by diphenylammonium triflate under microwave irradiation are described. Both armed and disarmed glycosyl-C1-hemiacetal donors were efficiently glycosylated in moderate to excellent yields without the need for any dry...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179217/ https://www.ncbi.nlm.nih.gov/pubmed/32131396 http://dx.doi.org/10.3390/molecules25051103 |
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author | Hsu, Mei-Yuan Lam, Sarah Wu, Chia-Hui Lin, Mei-Huei Lin, Su-Ching Wang, Cheng-Chung |
author_facet | Hsu, Mei-Yuan Lam, Sarah Wu, Chia-Hui Lin, Mei-Huei Lin, Su-Ching Wang, Cheng-Chung |
author_sort | Hsu, Mei-Yuan |
collection | PubMed |
description | Methods for direct dehydrative glycosylations of carbohydrate hemiacetals catalyzed by diphenylammonium triflate under microwave irradiation are described. Both armed and disarmed glycosyl-C1-hemiacetal donors were efficiently glycosylated in moderate to excellent yields without the need for any drying agents and stoichiometric additives. This method has been successfully applied to a solid-phase glycosylation. |
format | Online Article Text |
id | pubmed-7179217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71792172020-04-28 Direct Dehydrative Glycosylation Catalyzed by Diphenylammonium Triflate Hsu, Mei-Yuan Lam, Sarah Wu, Chia-Hui Lin, Mei-Huei Lin, Su-Ching Wang, Cheng-Chung Molecules Communication Methods for direct dehydrative glycosylations of carbohydrate hemiacetals catalyzed by diphenylammonium triflate under microwave irradiation are described. Both armed and disarmed glycosyl-C1-hemiacetal donors were efficiently glycosylated in moderate to excellent yields without the need for any drying agents and stoichiometric additives. This method has been successfully applied to a solid-phase glycosylation. MDPI 2020-03-02 /pmc/articles/PMC7179217/ /pubmed/32131396 http://dx.doi.org/10.3390/molecules25051103 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 | Communication Hsu, Mei-Yuan Lam, Sarah Wu, Chia-Hui Lin, Mei-Huei Lin, Su-Ching Wang, Cheng-Chung Direct Dehydrative Glycosylation Catalyzed by Diphenylammonium Triflate |
title | Direct Dehydrative Glycosylation Catalyzed by Diphenylammonium Triflate |
title_full | Direct Dehydrative Glycosylation Catalyzed by Diphenylammonium Triflate |
title_fullStr | Direct Dehydrative Glycosylation Catalyzed by Diphenylammonium Triflate |
title_full_unstemmed | Direct Dehydrative Glycosylation Catalyzed by Diphenylammonium Triflate |
title_short | Direct Dehydrative Glycosylation Catalyzed by Diphenylammonium Triflate |
title_sort | direct dehydrative glycosylation catalyzed by diphenylammonium triflate |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179217/ https://www.ncbi.nlm.nih.gov/pubmed/32131396 http://dx.doi.org/10.3390/molecules25051103 |
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