Diphenylethanediamine (DPEDA) as chiral selector: VII. Efficient HPLC resolution of a series of underivatized diarylcarbinols on a chiral stationary phase based on C5-amide-bonded N-3,5-dinitrobenzoyl-DPEDA

Chirality

Volumn 8, Issue 7, 1996, Pages 490-493

  Maier, Norbert M ^a   Uray, Georg ^a  

^a UNIVERSITY OF GRAZ   (Austria)

Author keywords

Arylarylmethanol; Chiral stationary phase; Diarylcarbinol; Enantioseparation

Indexed keywords

ETHYLENEDIAMINE; METHANOL DERIVATIVE;

ARTICLE; CHIRALITY; DRUG CONFORMATION; DRUG DETERMINATION; ENANTIOMER; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PRIORITY JOURNAL; STEREOISOMERISM;

BINDING SITES; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DINITROBENZENES; ETHYLENEDIAMINES; METHANOL; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 0030474187     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1520-636X(1996)8:7<490::AID-CHIR5>3.0.CO;2-F     Document Type: Article

References (9)

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3. Brown, E., Lézé, A., Touet, J. Preparative synthesis of optically pure orthosubstituted benzhydrols by asymmetric reductions of the corresponding benzophenones. Tetrahedron Asymmetry 3:841-844, 1992.
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7. Uray, G., Maier, N.M. Diphenylethanediamine (DPEDA) derivatives as chiral selectors VI. Enantioseparation of underivatized aryl substituted carboxylic acids on four differently linked diphenylethanediamine based CSPs. Enantiomers (in press), 1996.
8. Maier, N.M., Uray, G. Diphenylethanediamine (DPEDA) derivatives as chiral selectors V. Efficient normal phase high performance liquid chromatographic enantioseparation of underivatized chiral arylalcohols on four differently linked N-3,5-dinitrobenzoyl-DPEDA derived chiral stationary phases. J. Chromatogr. A 732:215-230, 1996.
9. Montaudo, G., Caccamese, S., Finocchiaro, P. Conformational preferences of bridged aromatic compounds: 1. Ortho substituted diphenylmethanes. J. Am. Chem. Soc. 93:4202-4207, 1971.