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V Analysis of Cellulose Pyrolyzate Formed at 350 — 375

V Analysis of Partial Hydrolyzale of Silk Fibroin

V Analysis of triazines in water from agricultural evaporation ponds.

V Analysis of Variance for Among and Within Treatments

V Analytical Results for Vinyl Acetate-on-Chromosorb 107 Samples

V and Fig. 4 summarize the principal data that have been obtained. In these experiments the percentage of transformed CH4 does not exceed 10 . This latter value corresponds to energy doses of 10 e.v., dissipated by the fission fragments. In the case of homogeneous irradiations the energy dissipated into the reaction system is equal to 3 X 10 e.v.

V and Figures 4, 5, and 6 present our essential results. Figures 4 and 5 show the relative magnitude of each term of Equation 5, the electric potential term being represented by the difference between the two curves for AGt and 2RT In with the

V and plotted in Figure 7 suggest that the larger the value of a i2, the larger the value of F12 . Comparing the solvents based on the same volume is recommended because it is easier and seems more conclusive.

V and there are carboxypeptidases that also belong to both families. Substrate specificity alone is not sufficient to rationally design an inhibitor for a new protease since it tells nothing about the active-site functional groups.

V Angiotensin-Converting Enzyme Inhibition by Central Amino Acid Analogues of Enalaprilat

V Anhydrides of Condensates of Sugars and Dicarbonyl Compounds 1

V Anhydro Sugars. Hydrofuranol Type

V Anhydro Sugars. Hydrofuranol Type S,5-Anhydrides

V Antifungal Activity of Triorqanogermanium

V Approximate Dimensions of Polypeptide Chain Coils

V Approximate work of adsorption at an air-water interface, for various organic groupings

V Aromas Developed by the Reactions of Carbonyl Compounds

V Ascorbate-Stimulated Transcriptional Activation of Different Collagen Types

V Assignments of Signals in the 13C-N.m.r. Spectra of Rhamnomannans from S. schenckii and C. stenoceras

V Assyometric Hydrogenation of Prochiral Olefins with

V Asymmetric polymer synthesis using ZnEtq-C-lDWD 1

V Atomic Exchange Energies

V Average Relaxation Time for Compounds Having Isotropic Motion

V Bacterial, Exocellular Polysaccharides Containing Neutral Sugar Residues

V Bond Angles Assumed for 4GT



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