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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
Descripción
Sumario: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.