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含粘蛋白型核心单元的新糖脂的合成。

Synthesis of neoglycolipids containing a mucin-type core unit.

作者信息

Horie R, Nakano K

机构信息

Biotechnology Research Laboratory, TOSOH Corporation, Kanagawa, Japan.

出版信息

Carbohydr Res. 1994 Nov 15;264(2):209-26. doi: 10.1016/s0008-6215(05)80007-2.

Abstract

The unnatural glycolipids O-beta-D-galactopyranosyl-(1-->4)-O-(2-acetamido- 2-deoxy-beta-D-glucopyranosyl)-(1-->3)-O-(2-acetamido-2-deoxy-alpha-D- galactopyranosyl)-(1-->1)-ceramide (1), O-beta-D-galactopyranosyl-(1-->4)-O-(2-acetamido-2-deoxy-beta-D-glucopyr anosyl) - (1-->6)-O-(2-acetamido-2-deoxy-alpha-D-galactopyranosyl)-(1-->1)-ceramid e (2), and O-beta-D-galactopyranosyl-(1-->4)-O-(2-acetamido-2-deoxy-beta-D- glucopyranosyl)-(1-->3)-O-[O-beta-D-galactopyranosyl-(1-->4)-(2-acetamid o-2- deoxy-beta-D-glucopyranosyl)-(1-->6)]-O-(2-acetamido-2-deoxy-alpha-D- galactopyranosyl)-(1-->1)-ceramide (3), and their beta-(1-->1)-linked isomers, were synthesized. The precursor oligosaccharides for 1, 2, and 3 were made by coupling O-2,3,4,6- tetra-O-acetyl-beta-D-galactopyranosyl)-(1-->4)-3,6-di-O-acetyl-2- deoxy-2-phthalimido-alpha,beta-D-glucopyranosyl trichloroacetimidate with tert-butyldiphenylsilyl 2-azido-4,6-O-benzylidene-2-deoxy-beta-D-galactopyranoside, tert-butyldiphenylsilyl 2-azido-3-O-benzoyl-2-deoxy-beta-D-galactopyranoside, and tert-butyl-diphenylsilyl O-(2,3,4,6-tetra-O-acetyl-beta-D-galactopyranosyl)-(1-->4)-O-(3,6-di-O-a cetyl-2 - deoxy-2-phthalimido-beta-D-glucopyranosyl)-(1-->3)-2-azido-2-deoxy-beta- D- galactopyranoside, respectively. These oligosaccharides were converted into their trichloroacetimidates, which were coupled with 3,2'-di-O-benzoyl ceramide. Deprotection of the coupling products gave the title compounds 1, 2, and 3.

摘要

合成了非天然糖脂O-β-D-吡喃半乳糖基-(1→4)-O-(2-乙酰氨基-2-脱氧-β-D-吡喃葡萄糖基)-(1→3)-O-(2-乙酰氨基-2-脱氧-α-D-吡喃半乳糖基)-(1→1)-神经酰胺(1)、O-β-D-吡喃半乳糖基-(1→4)-O-(2-乙酰氨基-2-脱氧-β-D-吡喃葡萄糖基)-(1→6)-O-(2-乙酰氨基-2-脱氧-α-D-吡喃半乳糖基)-(1→1)-神经酰胺(2)和O-β-D-吡喃半乳糖基-(1→4)-O-(2-乙酰氨基-2-脱氧-β-D-吡喃葡萄糖基)-(1→3)-O-[O-β-D-吡喃半乳糖基-(1→4)-(2-乙酰氨基-2-脱氧-β-D-吡喃葡萄糖基)-(1→6)]-O-(2-乙酰氨基-2-脱氧-α-D-吡喃半乳糖基)-(1→1)-神经酰胺(3)及其β-(1→1)-连接的异构体。1、2和3的前体寡糖是通过将O-2,3,4,6-四-O-乙酰基-β-D-吡喃半乳糖基-(1→4)-3,6-二-O-乙酰基-2-脱氧-2-邻苯二甲酰亚氨基-α,β-D-吡喃葡萄糖基三氯乙酰亚胺分别与叔丁基二苯基甲硅烷基2-叠氮基-4,6-O-亚苄基-2-脱氧-β-D-吡喃半乳糖苷、叔丁基二苯基甲硅烷基2-叠氮基-3-O-苯甲酰基-2-脱氧-β-D-吡喃半乳糖苷以及叔丁基二苯基甲硅烷基O-(2,三氯乙酰亚胺,然后将这些寡糖转化为它们的三氯乙酰亚胺,再与3,2'-二-O-苯甲酰基神经酰胺偶联。偶联产物的脱保护得到标题化合物1、2和3。

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