Carbohydrate Research p. 81 - 86 (1981)
Update date:2022-09-26
Topics: Synthesis Hydroxyl group Column chromatography NMR spectroscopy Mass spectrometry reflux Reaction Vessel Chloride Phthalimido β-D-galactopyranosyl β-D-glucopyranosyl
Ogawa, Tomoya
Nakabayashi, Satoru
A lactosaminyl donor, 3,6-di-O-acetyl-2-deoxy-2-phthalimido-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-glucopyranosyl chloride, was synthesized in 10 steps, starting from 1,3,4,6-tetra-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranose.Benzyl 3,6
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(1982)Doi:10.1021/jo00345a028
(1982)Doi:10.1021/jo00342a001
(1982)Doi:10.1021/ja00852a036
(1975)Doi:10.1002/anie.200801460
(2008)Doi:10.1007/BF00946417
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