Abstract
Phosphorylation of 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-D-glucose at the anomeric hydroxy group gave previously unknown triethylammonium 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-D-glucopyranosyl phosphonate, and successive treatment of the latter with decan-1-ol and aqueous iodine afforded triethylammonium 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyranosyl phosphate.
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Original Russian Text © B.F. Garifullin, R.R. Sharipova, A.D. Voloshina, M.A. Kravchenko, V.E. Kataev, 2018, published in Zhurnal Organicheskoi Khimii, 2018, Vol. 54, No. 9, pp. 1321–1324.
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Garifullin, B.F., Sharipova, R.R., Voloshina, A.D. et al. Synthesis and Antitubercular and Antibacterial Activities of Triethylammonium 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-D-glucopyranosyl Decyl Phosphate. Russ J Org Chem 54, 1333–1336 (2018). https://doi.org/10.1134/S1070428018090117
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DOI: https://doi.org/10.1134/S1070428018090117