Sugars displacement

Carbohydrate-specificity studies involving hemagglutination in-hibition61 100,587 and sugar displacement from Sephadex,587 and an immunosorbent of human blood-group A substance,587 gave essentially the same results. 

Amino sugars. Displacement of an anomeric bromine atom by an acetamino group is achieved when glycosyl bromides are treated with silver carbonate in MeCN in the dark. 

Washing and dewatering by air displacement of cakes are possible. AppHcations are in the treatment of minerals, in the sugar industry, and in the treatment of municipal sewage sludge and fillers like talc, clay, whiting, etc. 

The vertical recessed plate automatic press, shown schematically in Figure 15 and described previously, is another example of a horizontal belt pressure filter. Cycle times ate short, typically between 10 and 30 minutes, and the operation is fully automated. The maximum cake thickness is about 35 mm washing and dewatering (by air displacement) of cakes is possible. Apphcations include treatment of mineral slurries, sugar, sewage sludge, and fillers like talc, clay, and whiting. 

The Preparation of Halodeoxy Sugars by Displacement of Sulfonate Esters... 

Another deviation from the normal displacement reaction of primary tosylates occurs in nucleoside derivatives (39, 81) where cyclonucleosides and anhydronucleosides are formed by participation of a nitrogen atom (as in purine nucleosides) and oxygen atom (as in pyrimidine nucleosides ), respectively. Iodonucleosides can result from these reactions only if these cyclic compounds are prone to attack by iodide ion. Several new examples of unexpected reactions during the solvolysis of sulfonate esters in sugar derivatives have been recorded in the past few years (2, 4,5,7,15,44,62,63,94). 

The use of tetra-n-butylammonium fluoride (54) in an aprotic solvent such as acetonitrile may be more advantageous. Foster and colleagues (19, 37) have effected an SN2 type of reaction using this reagent in the conversion of l,2 5,6-di-0-isopropylidene-3-0-p-tolylsulfonyl-D-allofura-nose into the C-3 epimeric fluorodeoxy derivative. Note that whereas potassium fluoride is ineffective in displacing secondary sulfonate esters in sugars, tetra-n-butylammonium fluoride is capable of effecting a displacement with Walden inversion even in a furanose drivative. 

Two branched-chain sugars, methyl 3-azido-4,6-0-benzylidene-2,3,-dideoxy-3-C-(fluoromethyl)-a-D-flraZ)/ o-hexopyranoside and methyl 2-azido-4,6-0-benzylidene-2,3-dideoxy-2-C-(fluoromethyl)-) -D-r/to-hexo-pyranoside have been prepared through the usual displacement reactions. 

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