Contributions to chromatographic chiral recognition of permethrinic acid stereoisomers by a quinine carbamate chiral selector: evidence from X-ray diffraction, DFT computations, 1H NMR, and thermodynamic studies

Tetrahedron Asymmetry

Volumn 19, Issue 1, 2008, Pages 97-110

  Bicker, Wolfgang ^a   Chiorescu, Ion ^a   Arion, Vladimir B ^a   Lämmerhofer, Michael ^a   Lindner, Wolfgang ^a  

^a UNIVERSITY OF VIENNA   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

3 (2,2 DICHLOROVINYL) 2,2 DIMETHYLCYCLOPROPANE CARBOXYLIC ACID; 9 (2,6 DIISOPROPYLPHENYLCARBAMOYL)QUININE; CARBAMIC ACID DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; CYCLOPROPANE; INSECTICIDE; PERMETHRIN; QUININE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; CHIRALITY; CIS TRANS ISOMERISM; CRYSTAL STRUCTURE; DENSITY FUNCTIONAL THEORY; HYDROGEN BOND; MOLECULAR RECOGNITION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; STEREOISOMERISM; STRUCTURE ANALYSIS; THERMODYNAMICS; X RAY DIFFRACTION;

EID: 38349082958     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2007.11.037     Document Type: Article

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