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N-Hydroxyphthalimide Co-catalysed chemoselective oxidation of a secondary alcohol.

N-hydroxysuccinimide Cy5, an example of an activated water-soluble cyanine dye for the labeling of free amino groups.

N-I homogenous jump

N-I transition temperature Tc against the chain length L.

N-Inversion equilibrium in indolizidine.

N-Inversion equilibrium in quinolizidine.

N-l Cumulative RTD fiinciion

N-l Percolation Pond 120-N-2 Surface Impoundment

N-l Percolation Pond Area as it

N-ligands used as catalysts or for stabilizing metal centres in the electrochemical reduction of CO2. The first figure indicates the number of N-donor atoms in the ligand, the second gives the number of unsaturated N C bonds in the ligand and the third is an ordering number of ligands in the same class. Adapted with permission from . Copyright Royal Society of Chemistry

N-Linked a-Glycosides Obtained through Bromonium Activation of Pentenyl Glycosides in Acetonitrilel409-410

N-linked glycosylation of glycoproteins. Adapted from figures available on www.ionsource.com Card carbo nolink.htm.

N-Linked oligosaccharides in glyoproteins

N-linked oligosaccharides. A pentasaccharide core shaded gray is common to all N-linked oligosaccharides and serves as the foundation for a wide variety of N-linked oligosaccharides, two of which are illustrated

N-lsopropyl-thiadiazolyl sulfanilamide 19 was the first sulfonamide that showed antidiabetic properties in the clinics. Carbutamide 20 and tolbutamide 21 are also antidiabetics tolbutamide 21 has a shorter biological half-life than carbutamide 20, due to its methyl group instead of the chlorine atom in addition, tolbutamide does not show antibacterial activity. Glibendamide 22 is an antidiabetic drug with improved therapeutic properties.

N-Mannich base.

N-MethyF4-piperidynyl a-propynyl -cyclopentyl glycolate

N-methyl tetrahydrofolic acid.

N-methyl, N-formyl-4-hydroxy-P-phenylethylamine

N-Methyl-2-pyrrolidone.

N-Methylacetamide-water system

N-Methylanilinonaphthalene-2-sulphonylchloride

N-methylation of glutamine residues.

N-Methylation of Z- and Boc-Protected Amino Acids1941

N-methylol acrylamide and N-methylol methacrylamide.



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