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Solid oligosaccharides

Actilight P (powder, 95% ohgosaccharides) Actihght G (syrup, 75% (w/v) of solids. Oligosaccharides, =55% of solids) Profeed P95 and Profeed 95S (powder, 95% FOS) Profeed Maxflow (powder, 90% FOS) Profeed L95 (syrup, 95% FOS) Beghin-Meiji Industries France... [Pg.664]

One widely used method involving protected compounds is solid-phase synthesis (polymer-supponed reagents). This method has the advantage of requiring only a simple workup by filtration such as in automated syntheses, especially of polypeptides, oligonucleotides, and oligosaccharides. [Pg.4]

Carney CK.HarrySR,Sewell SL.WrightDW (2007) Detoxification Biominerals. 270 155-185 Castagner B, Seeberger PH (2007) Automated Solid Phase Oligosaccharide Synthesis. 278 289-309... [Pg.257]

P.H. Seeberger, Solid Support Oligosaccharide Synthesis and Combinatorial Carbohydrate Libraries, Wiley, New York, 2004. [Pg.68]

In addition, a novel fluorous support has been developed recently as an alternative to traditional polymer supports and applied successfully to oligosaccharide synthesis in combination with the trichloroacetimidate method [541]. Each intermediate in the fluorous oligosaccharide synthesis [542,543] could be obtained by simple fluorous-organic solvent extraction, and the reactions could be monitored by TLC, NMR and MS, in contrast to solid-phase reactions. Moreover, the new liquid-phase technique is anticipated to be easily applicable to the large-scale synthesis. [Pg.193]

Scheme 4.67 Solid-phase oligosaccharide synthesis on a Merrifield resin. Scheme 4.67 Solid-phase oligosaccharide synthesis on a Merrifield resin.
Solid Support Oligosaccharide Synthesis and Combinatorial Carbohydrate Libraries... [Pg.2]

Because of the lack of availability of several of these required methodologies, the initial attempts described below were ultimately not continued. However, they explored most of the fundamental issues that provide the basis for solid-phase oligosaccharide synthesis practiced today. In this chapter we focus on pioneering work carried out in the 1970s. [Pg.3]

Anderson and coworkers introduced a thioglycosidic linkage13 to the solid support in 1976 to afford the free reducing oligosaccharide after release from the support (Scheme 1.2A).14 Using a set of protecting groups similar to those mentioned above,... [Pg.3]

Scheme 1.1 Early solid-phase approaches to a-(l —>6)-linked oligosaccharides. Scheme 1.1 Early solid-phase approaches to a-(l —>6)-linked oligosaccharides.

See other pages where Solid oligosaccharides is mentioned: [Pg.73]    [Pg.73]    [Pg.620]    [Pg.15]    [Pg.200]    [Pg.504]    [Pg.157]    [Pg.525]    [Pg.10]    [Pg.79]    [Pg.13]    [Pg.418]    [Pg.222]    [Pg.230]    [Pg.2]    [Pg.24]    [Pg.72]    [Pg.103]    [Pg.110]    [Pg.190]    [Pg.190]    [Pg.191]    [Pg.192]    [Pg.233]    [Pg.377]    [Pg.277]    [Pg.143]    [Pg.18]    [Pg.54]    [Pg.193]    [Pg.2]    [Pg.2]    [Pg.4]    [Pg.4]   
See also in sourсe #XX -- [ Pg.230 , Pg.384 ]

See also in sourсe #XX -- [ Pg.45 ]




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