Issue 8, 1972

Stereochemistry of carbohydrate derivatives. Part IV. Crystal structure of 3,6-(acetylepimino)-3,6-dideoxy-1,2-O-isopropylidene-β-L-ido-furanose

Abstract

X-Ray crystallographic analysis, by a direct method, has confirmed the structure of title compound (2), the product of solvolysis of 3-acetamido-3-deoxy-1,2-O-isopropylidene-5,6-di-O-methylsulphonyl-α-D-glucofuranose (1) in 95% 2-methoxyethanol. Compound (2) crystallises in the monoclinic space group P21, with Z= 2 in a unit cell of dimensions a= 12·13, b= 9·51, c= 5·32 Å, β= 93·74°; the structure was refined to R 0·078 for 946 independent reflections.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1972, 937-942

Stereochemistry of carbohydrate derivatives. Part IV. Crystal structure of 3,6-(acetylepimino)-3,6-dideoxy-1,2-O-isopropylidene-β-L-ido-furanose

J. S. Brimacombe, J. Iball and J. N. Low, J. Chem. Soc., Perkin Trans. 2, 1972, 937 DOI: 10.1039/P29720000937

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