Improved Synthesis of 1-O-Acyl-β-d-Glucopyranose Tetraacetates

An improved synthesis of 1-O-acyl glucosyl esters that avoids the use of expensive Ag reagents as well as the hydrolysis of unstable glucosyl bromides is reported. Notably, β-configuration products were obtained exclusively in good yields.

Detalles Bibliográficos
Autores principales: Chen, Yu, Lu, Huan, Chen, Yanyu, Yu, Wansheng, Dai, Hui, Pan, Xianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154585/
https://www.ncbi.nlm.nih.gov/pubmed/28430152
http://dx.doi.org/10.3390/molecules22040662

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154585/
https://www.ncbi.nlm.nih.gov/pubmed/28430152
http://dx.doi.org/10.3390/molecules22040662

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