A chromatographic and computational study on the driving force operating in the exceptionally large enantioseparation of N-thiocarbamoyl-3-(4′-biphenyl)-5-phenyl-4,5-dihydro-(1H) pyrazole on a 4-methylbenzoate cellulose-based chiral stationary phase-Reference-Cited by-同舟云学术

A chromatographic and computational study on the driving force operating in the exceptionally large enantioseparation of N-thiocarbamoyl-3-(4′-biphenyl)-5-phenyl-4,5-dihydro-(1H) pyrazole on a 4-methylbenzoate cellulose-based chiral stationary phase

Published:2014-01 Issue: Volume:1324 Page:71-77
ISSN:0021-9673
Container-title:Journal of Chromatography A
language:en
Short-container-title:Journal of Chromatography A

Author:

Ortuso Francesco,Alcaro Stefano,Menta Sergio,Fioravanti Rossella,Cirilli Roberto

Publisher

Elsevier BV

Subject

Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry

Reference29 articles.

1. Unusual high enantioselectivity by a new HPLC chiral stationary phase

2. Synthesis and chromatographic resolution of some chiral four-carbon 2,2′-bridged biphenyls. Some unusually high selectivity factors

3. Separation and photoinduced transformations of the enantiomers of 3′,3′-dimethylspiro[2H-1-benzopyran-2,1′(2)oxaindans]

4. Extremely High Enantiomer Recognition in HPLC Separation of Racemic 2-(Benzylsulfinyl)benzamide Using Cellulose Tris(3,5-dichlorophenylcarbamate) as a Chiral Stationary Phase

5. Enantioseparation of selected chiral sulfoxides using polysaccharide-type chiral stationary phases and polar organic, polar aqueous–organic and normal-phase eluents

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