Abstract
The title trisaccharide was synthesized using methyl 1-thioglycoside building blocks. An acyclic analogue, methyl 3-O-(α-D-glycopyranosyl-oxyethyl)-α-D-glucopyranoside, which has an ethylene bridge in place of the galactosyl residue, was also synthesized.
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References
Jansson P-E, Lindberg B, Lindberg AA, Wohlin R (1981) Eur J Biochem 115:571–77.
Jazwinski SM, Lindberg AA, Kornberg A (1975) Virology 66:268–82.
Leontein K, Nilsson M, Norberg T (1985) Carbohydr Res 144:231–40.
Černý M, Pacák J (1958) Chem Listy 52:2090–93; Chem Abs (1959) 53:6093.
Lemieux RU, Hendriks KB, Stick RV, James K (1975) J Amer Chem Soc 97:4056–62.
Bock K, Pedersen C (1983) Adv Carbohydr Chem Biochem, 41:27–67.
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Norberg, T., Ritzen, H. Synthesis of methyl α-d-glucopyranosyl-(1–2)-α-d-galactopyranosyl-(1-3)-α-d-glucopyranoside and an acyclic analogue thereof for probing the carbohydrate-binding specificity of bacteriophage ϕX 174. Glycoconjugate J 3, 135–142 (1986). https://doi.org/10.1007/BF01049371
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DOI: https://doi.org/10.1007/BF01049371