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Collect. Czech. Chem. Commun. 1987, 52, 2248-2259
https://doi.org/10.1135/cccc19872248

Preparation of methyl 2,4-diacetamido-2,4,6-trideoxy-α-D-ido-, α-D-talo-, α-D-altro-, and α-D-mannopyranoside

Karel Čapeka, Jindra Čapkováa, Jiří Jarýa, Yurii A. Knirelb and Alexander S. Shashkovb

a Laboratory of Monosaccharides, Prague Institute of Chemical Technology, 166 28 Prague 6, Czechoslovakia
b N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the U.S.S.R., Moscow B-334, U.S.S.R.

Crossref Cited-by Linking

  • Banaszek Anna, Zaitsev Vladimir: 2,4-Diazido-2,4,6-trideoxy-l-hexopyranoses as valuable building units in the synthesis of natural products. Tet Asymm 2004, 15, 299. <https://doi.org/10.1016/j.tetasy.2003.11.018>
  • Tsvetkov Yury E., Shashkov Alexander S., Knirel Yuriy A., Zähringer Ulrich: Synthesis and NMR spectroscopy of nine stereoisomeric 5,7-diacetamido-3,5,7,9-tetradeoxynon-2-ulosonic acids. Carbohydrate Research 2001, 335, 221. <https://doi.org/10.1016/S0008-6215(01)00235-X>
  • Banaszek Anna, Pakulski Zbigniew, Zamojski Aleksander: The synthesis of derivatives of 2,4-diamino-2,4,6-trideoxy-d-gulo- and l-altro-hexopyranoses. Carbohydrate Research 1995, 279, 173. <https://doi.org/10.1016/0008-6215(95)00291-X>
  • Messner P, Bock K, Christian R, Schulz G, Sleytr U B: Characterization of the surface layer glycoprotein of Clostridium symbiosum HB25. J Bacteriol 1990, 172, 2576. <https://doi.org/10.1128/jb.172.5.2576-2583.1990>