Titlebook: Chiral Liquid Chromatography; W. J. Lough Book 1989 Chapman & Hall 1989 Enantiomer.chromatography.information.optimization.pharmaceutical.

DEIGN

書目名稱Chiral Liquid Chromatography影響因子(影響力)




書目名稱Chiral Liquid Chromatography影響因子(影響力)學(xué)科排名




書目名稱Chiral Liquid Chromatography網(wǎng)絡(luò)公開度




書目名稱Chiral Liquid Chromatography網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Chiral Liquid Chromatography被引頻次




書目名稱Chiral Liquid Chromatography被引頻次學(xué)科排名




書目名稱Chiral Liquid Chromatography年度引用




書目名稱Chiral Liquid Chromatography年度引用學(xué)科排名




書目名稱Chiral Liquid Chromatography讀者反饋




書目名稱Chiral Liquid Chromatography讀者反饋學(xué)科排名

Indurate

enfeeble

Chiral liquid chromatography: past and presentution of enantiomers from a racemate goes to Louis Pasteur who, in 1848, separated manually the non-identical crystals of the enantiomers of sodium ammonium tartrate (Pasteur, 1848). In 1874, Le Bel and Van’t Hoff independently proposed the ‘a(chǎn)symmetric carbon atom’ to account for the chirality of or

使害怕

Chiral derivatizationes. Derivatization of chiral substances is carried out with both chiral and achiral reagents. The latter may serve to block functional groups which may cause excessive band broadening on chiral columns (e.g, amines), or to introduce groups which interact favourably with the chiral stationary phase (

photopsia

Chiral ligand exchange chromatographynd ligand introduced to the chromatographic system. Chromatography thus performed is highly selective for the differentiation of chelatable solutes. Stereoselective resolution of isomeric ligands can be achieved if the system ligand is optically active and forms a chiral complex in the presence of a

抒情短詩

抒情短詩

Immobilized proteins as HPLC chiral stationary phasesal system including the complexation (or binding) of xenobiotic materials. As proteins are chiral polymers, it is not surprising that the binding of small enantiomeric molecules is often stereospecific. This is especially true for the serum proteins α.-acid glycoprotein (AGP) and albumin (SA).

FILTH

不安

Binding to cellulose derivativestive polymers. Like the interaction between an enzyme and its substrate, the polymer can lock on to the different stereochemistries of each enantiomer and provide chiral recognition. Proteins, oligosaccharides and celluloses have had the greatest degree of success, although usually bonded on to sili

Commonwealth

Binding to synthetic polymerso mimic and improve upon them. This expected development has taken place, and synthetic polymer chiral stationary phases (CSPs) are amongst the most recent to be made commercially available. As for natural polymers these synthetic polymers must first be immobilized on silica in some way to be of any