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VI Glycosidations with Phenyl Selenoribofuranoside 195

VI Glycosidic Derivatives of O-Glucosamine

VI Glycosidic linkage composition for arabinosyl residues in arabinan fraction of ultrafiltration retentate and in haze.

VI Glycosylguanidine Derivatives

VI Graduates Active in Education Department of Chemical and Petroleum Engineering University of Kansas

VI Group values for Estimating Heats of Formation of Nitroalkanes

VI Growth of microorganisms and production of antifungal agents in rizoshere soil of adzukibean in green house

VI GUM VULCANIZATE PROPERTIES OF TMO-AGE ELASTOMER

VI H Chemical Shifts for the Ring System of Isohexide Derivatives Chemical shifts

VI H NMR Chemical Shifts for Oligosaccharide Xylitols from the Carbohydrate-Protein

VI H NMR Spectra of Dihexulose Dianhydrides and Related Compounds

VI H- and F-N.m.r. Data for 2-Deoxy-2-ftaoro-hexopyranoseg and hexopyranosides

VI H2S04-Si02-Promoted One-Pot Benzylidenation Isopropylidenation-Acetylation, in Acetonitrile

VI Halide Ion Radii in the Lithium Halides

VI Haptens of GPLs from M. avium Serovars and Related NGPs

VI Heats and Entropies of Dissociation in Native Proteins

VI Helical Parameters and Conformation Angles in the Gellan Family of Polysaccharides

VI Hydration of Side Chains of Lysozyme

VI Hydrofornrylation of 1-Hexene in Acetone-

VI Hydrolysis of Natural Glycosides at 60

VI Hydrolysis Produces of Methylated Polysaccharide from CibbereUa fi fikuroP

VI Hyperfine interactions of various ROSF4 radicals at

VI illustrates in detail how the low-temperature parameters A, y, and D.LT can be used with the tabulated Debye function to obtain the specific heat values for Inconel X750 -STDA at 80 and 300 K, respectively.

VI illustrates still another important property of supports vis-a-vis homogeneous carbonyl complexes the ability to inaobilize coordinatively unsaturated sites. It is noteworthy that in solution Fe3 maintained a slight activity only in the presence of continued irradiation, whereas all measurements on the supported catalysts were made in the dark after photoactivation.

VI illustrates the effect of carbon monoxide on the activity of various fractions of cytochrome a. Almost the same inhibition is observed in Emasol4130inall preparations except Fraction S4, in which



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