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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.
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| Опубликовано в: : | Molecules |
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| Главные авторы: | , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
MDPI
2017
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6154585/ https://ncbi.nlm.nih.gov/pubmed/28430152 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/molecules22040662 |
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