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ChemInform Abstract: Direct Formation of β-Mannopyranosides and Other Hindered Glycosides from Thioglycosides.

✍ Scribed by D. CRICH; S. SUN


Publisher
John Wiley and Sons
Year
2010
Weight
38 KB
Volume
29
Category
Article
ISSN
0931-7597

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ChemInform Abstract: Direct Chemical Syn
✍ D. CRICH; S. SUN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 42 KB 👁 1 views

Direct Chemical Synthesis of β-Mannopyranosides and Other Glycosides via Glycosyl Triflates. -New and efficient methods to prepare β-mannopyranosides like (III) and (VI) are reported. The use of a 4,6-O-benzylidene-protected mannose as well as non-participating protecting groups on O-2 and O-3 are

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Direct Synthesis of β-Mannopyranosides by the Sulfoxide Method. -The activation of a glycosyl donor via the sulfoxide group followed by addition of a glycosyl acceptor in CH2Cl2 results in the formation of mannopyranosides in high yield and high β:α-ratios. Reducing the bulk of the O-2 protecting g