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Alditols structure

Figure 17 reproduces the analysis of the four-carbon region of the psr(trimethylsilyl)ated, reduced formose it shows possible alditol structures and their mass-spectrometric fragmentation patterns. Three four-carbon alditol structures are possible one branched, and two dia-stereoisomeric normal-chain forms. The chromatogram of the per(tri-... [Pg.207]

There are solitary examples of other alditol phosphates as components of this class of polymers. Arabinitol 1-phosphate is part of the S. pneumoniae type 17F capsular polysaccharide. o-Glucitol 6-phosphate is a component of the group-specific polysaccharide from group B Streptococcus, which has a most unusual, ramified structure. In a polysaccharide from Nocardia... [Pg.316]

Some of the multibranched complex glycans of hen ovomucoid have been analyzed by f.a.b.-m.s. together with e.i.-m.s. These glycans exhibit exceptional structural features, because their mannotriose core can be highly substituted, as shown in 25. All samples gave abundant [M+Na]" ions when analyzed as their permethylated alditols, and this permitted the... [Pg.60]

In a study completed during the early development of f.a.b.-m.s., both f.d. and f.a.b. were used to characterize 101 fractions containing neutral oligosaccharides isolated from human milk. Samples were examined as their peracetylated alditols. In subsequent work, the structures of two minor acidic oligosaccharides from human milk were investigated. The per-methylated derivatives were analyzed by f.a.b.-m.s., and their compositions and sequences were defined by the f.a.b. data. Methylation analysis and partial formolysis were the other principal methods used. [Pg.70]

Oligosaccharides were isolated from PMII by weak acid hydrolysis and separation by SEC and HPAEC-PAD. The isolated oligosaccharides were desalted, reduced and methylated. GC-MS analysis of the partially methylated alditol acetates has been used to reveal the structure of the oligosaccharides. [Pg.619]

Multiple-ion monitoring is, however, of considerable value in structural studies, but only if model compounds of known structure are available for comparison. Such an approach has been used in the study of the carbohydrate structures of glycoproteins from different tissues.50 Separation of glycopeptides obtained from various tissues was performed on columns of concanavalin A-Sepharose. Structural analysis by multiple-ion monitoring of partially methylated, alditol acetates derived from the various fractions indicated that the glycopeptides were separated according to the linkage pattern of mannose (see Fig. 1). [Pg.403]

In addition to these physical studies at the Bureau, Tipson was able to return to his synthetic interests, both alone and in collaboration with other staff members. He was especially pleased to prepare D-talose in crystalline form, an accomplishment that had eluded Emil Fischer. Pursuing his longstanding interest in the reaction of sulfonic esters with iodide and following an earlier observation that the tetratosyl ester of erythritol is converted into butadiene by the action of sodium iodide and zinc, he demonstrated (with A. Cohen) that nonterminal unsaturation may be conveniently introduced into alditol derivatives by reaction of contiguous secondary sulfonates with sodium iodide and zinc dust in boiling A.A-dimethylformamide. This Tipson-Cohen reaction subsequently proved of great utility in other hands for the conversion of more complex carbohydrate structures into vicinal dideoxy derivatives. [Pg.425]

L. E. Fellows, E. A. Bell, D. G. Lynn, F. Pilkiwicz, I. Miura, and K. Nakanishi, Isolation and structure of an unusual cyclic amino alditol from a legume, J. Chem. Soc., Chem. Commun. (1979) 977-978. [Pg.277]

In connection with the structure of glycoproteins, Lloyd and Kabat studied the separation of six alditol acetates,452 and Kim and coworkers57 examined the separation of L-fucitol, D-glucitol, D-manni-tol, and galactitol. Alditol acetates have been used in studies on... [Pg.63]

The separation and identification of disaccharides is often an important step in the elucidation of the structure of a natural polysaccharide, and Percival484 has published useful data on the O-trimethyl-silyl derivatives of a variety of disaccharides and their reduction products. In some instances, the trimethylsilyl ethers of the disaccharide alditols have lower retention times than those of the disaccharide derivatives. The per-O-trimethylsilyl derivatives of gentiobi-itol and maltitol were encountered in studies on the structure of Pneumococcus Type II capsular polysaccharide.4843... [Pg.69]

The key sequence in the determination of the structures of 2,5-anhydro-D-mannose (2) and -D-talose (4) was their reduction to the corresponding 2,5-anhydroalditols (5 and 6) and identification of the asymmetric dialdehyde (7) resulting from oxidation of the anhydro-alditols with periodate.37,43... [Pg.186]

Problem 22.25 What is the structure of the aldopentose o-ribose, a constituent of ribonucleic acids (RNA), if it gives the same osa2one as o-arabinose (Problem 22.24) and is reduced to an optically inactive alditol ... [Pg.502]

Problem 22.34 (a) Write shorthand structures for the three o-2-ketohexoses other than o-fructose. (b) Which one does not give a meso alditol on reduction (c) Which one gives the same osazone as does D-galactose (Problem 22.22)7 <... [Pg.507]

As regards the l,l-bis(acylamido)-l-deoxyalditols, the first structural study was that of Fletcher and coworkers,69 who conducted oxidations with lead tetraacetate. These authors postulated an empirical relationship between the position of the oxidation curve in a graph and the number of hydroxyl groups present. They compared the curves afforded by a series of l,l-bis(acetamido)-l-deoxyalditols with those of alditols having the same number of free hydroxyl groups, and observed a close correspondence. At present, periodate oxidation is widely applied to these mono- or di-saccharide derivatives. Under controlled conditions, the methylation technique can also be applied.42... [Pg.109]

Diols and polyols can participate in equilibria with boric acid in aqueous solution. The stability of polyolborates is determined by the number of OH groups in cis positions. Complexes with polyols are more stable than with diols, and 1,2-diol complexes are more stable than their 1,3-diol counterparts (Table 10) since the resulting five-membered chelate ring is unstrained.75120 In the case of 1,3,5-triols stable cage-like structures (5) and (6) are favored. Open-chain or five-membered cyclic polyols form more stable chelate complexes than their six-membered counterparts.120 Thus, chelates from alditols and ketohexoses are more stable than the corresponding aldose chelates (Table 10). Many polyols allow quantitative titrimetric determination of boric acid. Of these, mannitol remains the most widely used reagent on the basis of availability, cost and ease of handling.75... [Pg.95]

The more stable boron chelates can be isolated even from aqueous solution, whereas those of lower stabilities are only accessible from non-aqueous media. Catechol- and inositol-borates (3, 5 and 6) possesses a well-defined monomeric structure,75 whereas those obtained from monosaccharides and alditols are polymeric.121 A crystal structure determination122 has been carried out for sodium scyUo-inositol diborate (6). [Pg.95]


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See also in sourсe #XX -- [ Pg.258 ]




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