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Directed phosphorylation of 2-C-hydroxymethyl-2,3:5,6-di-O-isopropylidene-D-mannofuranose

✍ Scribed by E.V. Lipovtsin; M.P. Koroteev; L.K. Vasyanina; E.E. Nifant"ev

Book ID
111607464
Publisher
Springer
Year
2003
Tongue
English
Weight
307 KB
Volume
52
Category
Article
ISSN
1573-9171

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A second crystalline diacetonide, the title compound, C 13 H 20 O 7 , has been isolated from the sequential treatment of d-tagatose with aqueous sodium cyanide, followed by acetone in the presence of acid. Structural ambiguities with regard to the size of both the lactone and ketal rings are resolve

X-ray and conformational investigation o
X-ray and conformational investigation of 6-deoxy-6-C-(1,5-di-O-acetyl-2,3-O-isopropylidene-β-d-allo-pentofuranos-5-yl)-1,2:3,4-di-O-isopropylidene- α-d-galactopyranose and 6-C-(benzyl 5-deoxy-2,3-O-isopropylidene-β-d-ribofuranosid-5-yl)-1,2:3,4-di-O-isopropylidene- d-glycero-α-d-galacto-hexopyranose
✍ Janusz W. Krajewski; Wojciech Karpiesiuk; Anna Banaszek 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 523 KB

The structures of the title compounds (2b and 3) have been investigated in the solid state by X-ray methods. The crystals of 2b are monoclinic, space group P2,, and of 3 orthorhombit, space grtup P2,2,2,. The cell dimensions are: for 2b, a = 9.910(2), b = 11;745W, c = 11.810(3) A, /3 = 97.32(l)"; a