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One-Pot, Highly Stereoselective Synthesis of Dithioacetal-α,α-Diglycosides
A one-step access to dithioacetal-α,α-diglycosides is reported. The synthetic strategy is based on the thioacetalization of aldehydes or ketones via highly stereoselective ring-opening of 1,6 anhydrosugars with bis(trimethylsilyl)sulfide.
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| Udgivet i: | Molecules |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
MDPI
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6017313/ https://ncbi.nlm.nih.gov/pubmed/29662042 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/molecules23040914 |
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