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An efficient synthesis of D-galactose-based multivalent neoglycoconjugates
[摘要] In this work, the synthesis of dimeric, trimeric and tetrameric D-galactose-based neoglycoconjugates is reported. The monosaccharide ligand was prepared in 5 straightforward steps from D-galactose using the Doebner modification of the Knoevenagel reaction for chain elongation. The ligand was coupled to 1,4-butanediamine, tris-(2-ethylamino)amine, pentaerythrityltetramine and PAMAM dendrimers (1,4-butanodiamine core G0 and 1,12-dodecanediamine core G0). The unprotected glycodendrimers were purified by size-exclusion chromatography (SEC). This was the only step in which a chromatographic method was employed throughout the synthetic route. This is a new and efficient strategy for the preparation of neoglycoconjugates.
[发布日期]  [发布机构] 
[效力级别]  [学科分类] 化学(综合)
[关键词] glycodendrimers;D-galactose;synthesis;pentaerythrityltetramine;PAMAM [时效性] 
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