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Direct and Stereoselective Synthesis of α-Linked 2-Deoxy-Glycosides
[Image: see text] α-Linked 2-deoxy-glycosides were conveniently obtained by employing a glycosyl donor having a participating (S)-(phenylthiomethyl)benzyl moiety at C-6, whereas 2,6-di-deoxy-α-glycosides could be prepared by BF(3)•Et(2)O promoted activation of allyl glycosyl donors.
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2008
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2631667/ https://ncbi.nlm.nih.gov/pubmed/18763796 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol801833n |
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