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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...

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Detalles Bibliográficos
Autores principales: You, Xueying, Cai, Yifei, Xiao, Chenyu, Ma, Lijuan, Wei, Yong, Xie, Tianpeng, Chen, Lei, Yao, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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.
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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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