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Stereoselective Synthesis of 2-Deoxythiosugars from Glycals
2-deoxythiosugars are more stable than 2-deoxysugars occurring broadly in bioactive natural products and pharmaceutical agents. An effective and direct methodology to stereoselectively synthesize α-2-deoxythioglycosides catalyzed by AgOTf has been developed. Various alkyl thiols and thiophenols were...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696349/ https://www.ncbi.nlm.nih.gov/pubmed/36432078 http://dx.doi.org/10.3390/molecules27227979 |
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author | You, Xueying Cai, Yifei Xiao, Chenyu Ma, Lijuan Wei, Yong Xie, Tianpeng Chen, Lei Yao, Hui |
author_facet | You, Xueying Cai, Yifei Xiao, Chenyu Ma, Lijuan Wei, Yong Xie, Tianpeng Chen, Lei Yao, Hui |
author_sort | You, Xueying |
collection | PubMed |
description | 2-deoxythiosugars are more stable than 2-deoxysugars occurring broadly in bioactive natural products and pharmaceutical agents. An effective and direct methodology to stereoselectively synthesize α-2-deoxythioglycosides catalyzed by AgOTf has been developed. Various alkyl thiols and thiophenols were explored and the desired products were formed in good yields with excellent α-selectivity. This method was further applied to the syntheses of S-linked disaccharides and late-stage 2-deoxyglycosylation of estrogen, L-menthol, and zingerone thiols successfully. |
format | Online Article Text |
id | pubmed-9696349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96963492022-11-26 Stereoselective Synthesis of 2-Deoxythiosugars from Glycals You, Xueying Cai, Yifei Xiao, Chenyu Ma, Lijuan Wei, Yong Xie, Tianpeng Chen, Lei Yao, Hui Molecules Communication 2-deoxythiosugars are more stable than 2-deoxysugars occurring broadly in bioactive natural products and pharmaceutical agents. An effective and direct methodology to stereoselectively synthesize α-2-deoxythioglycosides catalyzed by AgOTf has been developed. Various alkyl thiols and thiophenols were explored and the desired products were formed in good yields with excellent α-selectivity. This method was further applied to the syntheses of S-linked disaccharides and late-stage 2-deoxyglycosylation of estrogen, L-menthol, and zingerone thiols successfully. MDPI 2022-11-17 /pmc/articles/PMC9696349/ /pubmed/36432078 http://dx.doi.org/10.3390/molecules27227979 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication You, Xueying Cai, Yifei Xiao, Chenyu Ma, Lijuan Wei, Yong Xie, Tianpeng Chen, Lei Yao, Hui Stereoselective Synthesis of 2-Deoxythiosugars from Glycals |
title | Stereoselective Synthesis of 2-Deoxythiosugars from Glycals |
title_full | Stereoselective Synthesis of 2-Deoxythiosugars from Glycals |
title_fullStr | Stereoselective Synthesis of 2-Deoxythiosugars from Glycals |
title_full_unstemmed | Stereoselective Synthesis of 2-Deoxythiosugars from Glycals |
title_short | Stereoselective Synthesis of 2-Deoxythiosugars from Glycals |
title_sort | stereoselective synthesis of 2-deoxythiosugars from glycals |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696349/ https://www.ncbi.nlm.nih.gov/pubmed/36432078 http://dx.doi.org/10.3390/molecules27227979 |
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