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D-Glucose reaction under basic conditions.

D-glucose structure data

D-Glucose to 2-KGA fermentation.

D-Glucose under the microscope.

D-Glucose-D-Ribose Interconversion.

D-Glucuronic acid

D-Glyceraldehyde and D-glucose. These sugars have the same configuration at the asymmetric carbon atom farthest from the carbonyl group. Both belong to the D series. Asymmetric carbons are shown in blue.

D-Gulopyranose, -gab o sine E and L-lyxopyranose.

D-Guloseptanose derivative.

D-HMQC spectra obtained on HA

D-HMQC spectrum of glycyl-i-alanine at 70 kHz MAS at the mag-

D-Iog E curves of strips of film coated with 0.2 fim AgBr emulsion containing 5.5 X 10 mol Dye 3 mol AgBr, which was exposed to light with exposure amount E in a sample tube in an ESR spectrometer and developed. The exposure amount for the ESR measurement is shown by the arrow.

D-Ketoses containing three- four, five, and six carbon atoms The keto group is shown in blue. The asymmetric center farthest from the keto group, which determines the D designation, is shown in red.

D-l Method for Estimating Strain in Dents

D-l The Re03 structure. The perovskite structure is obtained from this one by insertion of a large cation at the center of the cube.

D-LC fractionation of high molecular weight PS-i -PI molecular weight portion of the PS block. RPLC fractionates the PI block while NPLC fractionates the PS block. The range of the fraction collected is indicated with small vertical bars. Reproduced from with per-

D-LC separation of a low molecular weight PS-fc-PI

D-log E curves showing latent jading in 0.2 pin AgBr emulsion to which Dye 3 was added. Coated film was exposed for 10

D-log I curve of the microcolumn sample used for examination with SEN.

D-Mannitol P-amino thio ligands for additions of ZnEt2 to aldehydes.

D-Mannitol-derived phospholane catalysts in asymmetric MBH reactions.

D-Mannuronic and L-guluronic repeat units of alginic acid

D-MeAia3 and olefin cyclosporin analogs.

D-model for Grignard reagent formation. Since R, Ri, and S were assumed to have identical properties, they could be treated as a single intermediate T. which may either return to the surface and react with magnesium or undergo coupling in solution. Differences in the nature of the radical intermediates R. R,., and S were ignored.

D-model for the single reactive intermediate T.



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