Synthesis of chitosan 3,6-diphenylcarbamate-2-urea derivatives and their applications as chiral stationary phases for high-performance liquid chromatography

Journal of Chromatography A

Volumn 1365, Issue , 2014, Pages 86-93

  Zhang, Lili ^a   Shen, Jun ^a   Zuo, Wenli ^a   Okamoto, Yoshio ^a,b  

^a HARBIN ENGINEERING UNIVERSITY   (China)

^b NAGOYA UNIVERSITY   (Japan)

Author keywords

Chiral recognition; Chiral stationary phases; Chitosan; HPLC; Phenylcarbamate

Indexed keywords

CHITOSAN; CHLORINE COMPOUNDS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SILICA; SILICA GEL;

CHIRAL RECOGNITION; CHIRAL STATIONARY PHASIS; CHITOSAN DERIVATIVES; DEACETYLATED CHITOSANS; ELECTRON-DONATING SUBSTITUENTS; ELECTRONWITHDRAWING; HPLC; PHENYLCARBAMATE;

STEREOCHEMISTRY;

CHITOSAN 3,6 DIPHENYLCARBAMATE 2 UREA DERIVATIVE; CHITOSAN DERIVATIVE; CHLOROFORM; PROTON; UNCLASSIFIED DRUG; CARBAMIC ACID DERIVATIVE; CHITOSAN; SILICA GEL; UREA;

ARTICLE; CHEMICAL PHENOMENA; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; CHIRAL CHROMATOGRAPHY; CHIRAL STATIONARY PHASE; CONTROLLED STUDY; ENANTIOSEPARATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; INFRARED SPECTROSCOPY; MOLECULAR RECOGNITION; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS; ANALOGS AND DERIVATIVES; CHEMISTRY; DEVICES; PROCEDURES; STEREOISOMERISM; STRUCTURE ACTIVITY RELATION;

CHITOSAN; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; PHENYLCARBAMATES; SILICA GEL; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP; UREA;

EID: 84908070261     PISSN: 00219673     EISSN: 18733778     Source Type: Journal    
DOI: 10.1016/j.chroma.2014.09.002     Document Type: Article

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