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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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Detaylı Bibliyografya
Asıl Yazarlar: Park, Jin, Boltje, Thomas J., Boons, Geert-Jan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2008
Konular:
Online Erişim: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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