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Synthesis and Ring Structure of 7-Acetamido-7-deoxy-L-galacto-heptulose
1Retired. Inquiries concerning this paper should be directed to the Division of Analytical Chemistry, National Bureau of Standards, Washington, D.C. 20234.
Abstract:
7-Acetamido-7-deoxy-L-galacto-heptulose was prepared by oxidation of l-acetamido-l-deoxy-D-glycero-D-galacto-heptitol with Acetobacter suboxydans. The new acetamido-deoxy-L-heptulose was shown to be a pyranose by comparison with β-D-fructopyranose. The following equations represent the optical rotation of 7-acetamido-7-deoxy-α-L-galacto-heptulopyranose in water at 20 °C and 3.5 °C, respectively:
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