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Tables their simple derivatives

R. F. Butterworth and S. Hanessian, Tables of the properties of deoxy sugars and their simple derivatives, Adv. Carbohydr. Chem. Biochem. 26 279 (1971). [Pg.124]

Bray, H. G and Stacey, M., Blood Group Polysaccharides, 4, 37-55 Brimacombe, J. S. See How, M. J. Butterworth, Roger F and Hanes-sian, Stephen, Tables of the Properties of Deoxy Sugars and Their Simple Derivatives, 26, 279-296... [Pg.385]

TABLES OF THE PROPERTIES OF DEOXY SUGARS AND THEIR SIMPLE DERIVATIVES... [Pg.279]

Bourne, E. J. See also. Barker, S. A. Bouveng, H. O., and Lindberg, B., Methods in Structural Polysaccharide Chemistry, 15, 53-89 Brady, Robert F., Jr., Cyclic Acetals of Ketoses, 26, 197-278 Bray, H. G., D-Clucuronic Acid in Metabolism, 8, 251-275 Bray, H. G., and Stacey, M., Blood Group Polysaccharides, 4, 37-55 Brimacombe, j. S. See How, M. J. Butter worth, Roger F and Hanes-siAN, Stephen, Tables of the Properties of Deoxy Sugars and Their Simple Derivatives, 26, 279-296... [Pg.453]

Buttehworth, Roger F., and Haness-lAN, Stephen, Tables of the Properties of Deoxy Sugars and Their Simple Derivatives, 26, 279-296... [Pg.523]

The esters of lycoctonine with anthranilic acid and its AT-acyl derivatives are highly toxic, and the Delphinium species in which they occur are sources of cattle poisoning these alkaloids are, therefore, of considerable economic importance, and it is to be hoped that the long period during which their chemistry has been neglected is now coming to an end. The studies on record now show that purification of these labile alkaloids is troublesome, and only small quantities of the bases have been isolated hitherto. Chemical work has therefore been confined to the characterization of the alkaloids and the elucidation of their relation to lycoctonine by identification of the acid fragment obtained on hydrolysis. Properties of the bases and their simple derivatives are recorded in Table 18. [Pg.325]

N-Benzylamides are recommended when the corresponding acid is liquid and/or water-soluble so that it cannot itself serve as a derivative. Phe benzylamides derived from the simple fatty acids or their esters are not altogether satisfactory (see Table below) those derived from most hydroxy-acids and from poly basic acids or their esters are formed in good yield and are easily purified. The esters of aromatic acids yield satisfactory derivatives but the method must compete with the equally simple process of hydrolysis and precipitation of the free acid, an obvious derivative when the acid is a solid. The procedure fails with esters of keto, sul phonic, inorganic and some halogenated aliphatic esters. [Pg.394]

Gifford and Hanna tested their simple box model for particulate matter and sulfur dioxide predictions for annual or seasonal averages against diffusion-model predictions. Their conclusions are summarized in Table 5-3. The correlation coefficient of observed concentrations versus calculated concentrations is generally higher for the simple model than for the detailed model. Hanna calculated reactions over a 6-h period on September 30, 1%9, with his chemically reactive adaptation of the simple dispersion model. He obtained correlation coefficients of observed and calculated concentrations as follows nitric oxide, 0.97 nitrogen dioxide, 0.05 and rhc, 0.55. He found a correlation coefficient of 0.48 of observed ozone concentration with an ozone predictor derived from a simple model, but he pointed out that the local inverse wind speed had a correlation of 0.66 with ozone concentration. He derived a critical wind speed formula to define a speed below which ozone prediction will be a problem with the simple model. Further performance of the simple box model compared with more detailed models is discussed later. [Pg.226]

The data shown in Table 2 illustrate the general paucity of comparative toxicity data within an isosteric series of chemicals. In this Table a variety of toxic end-points observed for benzene and naphthalene have been compared with those of their simple heterocyclic analogues, and it is clear that it is almost impossible to derive chemical structure-biological activity relationships from the published literature for even such a simple series of compounds. Even basic estimates of mammalian toxicity such as LD50 values cannot be accurately compared due either to the absence of relevant data or the noncomparability of those available. Thus in a field where there are little comparative data on the relative toxicity to mammals of pyrrole, thiophene and furan for example, it is difficult to relate chemical structure to biological activity in historical heterocyclic poisons such as strychnine (3) and hemlock [active agent coniine (4)]. [Pg.114]

Veracevine (11), cevine (15), or cevagenine (14) may be oxidized with bismuth oxide to the same 8-lactone (27) (45,52). This undergoes the simple reactions shown in Scheme 7 to give the other five-membered ring A derivatives 28-31. Two natural products (32,33) having five-membered A rings and 8-lactone structures have been isolated and are recorded along with their synthetic derivatives in Table IX. [Pg.186]

More Complicated Molecules.—Calculations have been reported on a number of more complicated molecules, as indicated in Table 4. The work on BFa and SOa, and on NH3 and NF3, is of particular interest since these are the simplest symmetric top structures for which the calculation is practical, and for which there exist sufficient spectroscopic data to make it worthwhile for symmetric top molecules there are extra observable vibration-rotation interaction constants associated with the vibrational degeneracy that provide further information on the force field (see Table 3). Formaldehyde and ethylene, and their simple halogen derivatives, and also methane, are obvious candidates for further work. [Pg.157]

In summary, experimental data on the isomeric abundances at anomeric equilibrium reveal that the preference for the axial position depends on several, interconnected factors which were clarified in surveys on carbohydrate stereochemistry, and these provided a background for ensuing theoretical studies. The elucidation of this relationship in complex carbohydrates is greatly facilitated by measurements on the simple derivatives of oxane, and qualitative trends have already been established. Table II illustrates sever possibilities of the quantification of the energetic aspect of the anomeric effect. The procedure most frequently used, based on Eq. 7, suffers from the ambiguity of the A values for the oxane ring and by their presumed variation with solvent. [Pg.69]

The 13C NMR spectral data of simple flavones and their methyl derivatives, luteolin (6), cirsilineol (9), viscidulin III (64), rivularin (113) are given in Table 13. [Pg.285]


See other pages where Tables their simple derivatives is mentioned: [Pg.535]    [Pg.537]    [Pg.547]    [Pg.549]    [Pg.564]    [Pg.471]    [Pg.473]    [Pg.527]    [Pg.528]    [Pg.32]    [Pg.59]    [Pg.112]    [Pg.424]    [Pg.518]    [Pg.173]    [Pg.1005]    [Pg.4]    [Pg.415]    [Pg.52]    [Pg.152]    [Pg.277]    [Pg.754]    [Pg.309]    [Pg.52]    [Pg.58]   
See also in sourсe #XX -- [ Pg.26 , Pg.296 ]




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Derivatives, table

Their Derivatives

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