It has been revealed that the oligosaccharide is an important factor in many areas of life processes, embryonic growth, differentiation, aging, immunity and carcinogenesis. Many researches have been conducted to understand the functions in biological systems and structure-activity relationship of oligosaccharides. For the structure-based studies, it is necessary to synthesize oligosaccharides with confirmed structure so as to evaluate their activity. Throughout the synthesis of oligosaccharides, glycosylation, protection and deprotection processes are repeated for every glycosidic linkage formed. Thus, in order to synthesize oligosaccharides effectively, the glycosyl donor and acceptor, as well as the protecting agents are vitally important. For this reason, there is much research activity in finding glycosyl donors and acceptors with suitable properties.
In recent years, the glucose derivative 1, with thioformimidate as a leaving group, was developed by Mukaiyama and his co-workers.1) This reagent is a glycosyl donor with high reactivity and stability. 1 is activated with a catalytic amount of TfOH in the presence of MS5A and reacts with a glycosyl acceptor to provide a disaccharide in a quantitative yield. Furthermore, by choosing the appropriate solvents, α- or β-glycosides can be obtained selectively. The glycosyl acceptors with a fluorine atom or an ethylthio group at 1-position were also used and the resulting disaccharides can also be used as glycosyl donors.
In addition, the utility of p-methoxyphenyl glycosides has been reported.2) The p-methoxyphenyl group is a useful anomeric protective group which is stable under most of the conditions used in oligosaccharide synthesis. It is removed selectively by treatment with 2,3-dichloro-5,6-dicyano-pbenzoquinone and ceric ammonium nitrate (IV), to give the corresponding hemiacetals. Also the p-methoxyphenyl glycosides are converted in one step into the corresponding glycosyl halides and thiophenyl glycosides in high yields and can be used as glycosyl donors.
The followings are glycosyl donors in which the anomeric position is activated, including 1, p-methoxyphenyl glycosides, glycosyl acceptors and activating agents that can be obtained from TCI. TCI is pleased to supply these reagents for your needs in the research of oligosaccharides and related studies.
Glycosyl Donors
Reagents for Glycosyl Donor Synthesis
MP Glycosides & Related Reagents
Glycosyl Acceptors
Activating Agents
Enzyme
Enzyme Substrates
Glycosyl Donors
・Imidate Sugars
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・Thioglycosides
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・Halogeno Sugars
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・Others
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Reagents for Glycosyl Donor Synthesis
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MP Glycosides & Related Reagents
・Galactose
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・Galactosamine
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| M1643 | 4-Methoxyphenyl 3-O-Allyl-2-azido-4,6-O-benzylidene-2-deoxy-beta-D-galactopyranoside |
・Glucose
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| M1630 | 4-Methoxyphenyl 2,3,4,6-Tetra-O-acetyl-beta-D-glucopyanoside |
| M1642 | 4-Methoxyphenyl 2,4,6-Tri-O-acetyl-3-O-benzyl-beta-D-glucopyranoside |
・Glucosamine
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・Mannose
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| M1647 | 4-Methoxyphenyl 2,3,4,6-Tetra-O-acetyl-alpha-D-mannopyranoside |
・Disaccharides
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・Deprotecting Reagents
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| C1806 | Ammonium Cerium(IV) Nitrate |
| D1070 | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone |
Glycosyl Acceptors
・Galactose
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・Galactosamine
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・Glucose
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・Glucosamine
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・Mannose
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| T1459 | 1,3,4,6-Tetra-O-acetyl-beta-D-mannopyranose |
・Disaccharides
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| M1686 | Gal[26Bn]beta(1-4)Glc[236Bn]-beta-MP |
| M1726 | Gal[236Bn]beta(1-4)Glc[236Bn]-beta-MP |
| M1727 | Gal[246Bn]beta(1-4)Glc[236Bn]-beta-MP |
Activating Agents
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Enzyme
Enzyme Substrates
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| A1614 | Nomega-(2-Acetamido-2-deoxy-beta-D-glucopyranosyl)-Nalpha-(tert-butoxycarbonyl)-L-asparagine |
| G0297 | N-GlcNAc-Biotin |
Literature
2) M. Mori, Y. Ito, T. Ogawa, Carbohydr. Res., 1989, 192, 131 [DOI]; Y. Matsuzaki, Y. Ito, T. Ogawa, Tetrahedron Lett., 1992, 33, 4025 [DOI]; A. Dan, Y. Ito, T. Ogawa, J. Org. Chem., 1995, 60, 4680 [DOI]; C. Murakata, T. Ogawa, Carbohydr. Res., 1992, 235, 95 [DOI]; H. Kuyama, T. Nukada, Y. Nakahara, T. Ogawa, Tetrahedron Lett., 1993, 34, 2171 [DOI]; Z. Zhang, G. Magnusson, Carbohydr. Res., 1996, 295, 41 [DOI]; H. Ando, Y. Koike, H. Ishida, M. Kiso, Tetrahedron Lett., 2003, 44, 6883 [DOI].
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