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5-Chloro-5-deoxy-1,2-O-isopropylidene-3-methanesulphonyl-4-thio-β-L-arabinofuranose

✍ Scribed by Clegg, W.


Book ID
117859850
Publisher
International Union of Crystallography
Year
1975
Weight
315 KB
Volume
31
Category
Article
ISSN
0567-7408

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The syntheses have been described of the 2-acetamido-2-deoxy derivatives of 5-thio-D-glucose lm3, 5-thio-D-mannose 4, 5-thio-D-allose 5, 3-acetamido-3-deoxy5thio-D-xylose6, and 4-acetamido-4-deoxy-5-thio-r\_-lyxose6. We now report the syntheses of 3-amino-3-deoxy-5-thio-D-allose hydrochloride and a

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The relative configuration of the title compound, C~9~H~14~NO~5~, formed by catalytic hydrogenation of an azidolactone, has been established by X-ray crystallographic analysis. The absolute configuration was determined by the use of 2,3-__O__-isopropylidene-L-lyxono-1,4-lactone as the carbohydrate s