γ‐Cyclodextrin as chiral mobile phase additive in the HPLC separation of the atropisomers of some  N ‐arylthiazoline‐2‐thiones and  N ‐arylthiazoline‐2‐ones: Attempts to quantify the effect of selected structural parameters | Zendy

Roussel Christian | Zendy; Favrou Anita | Zendy

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γ‐Cyclodextrin as chiral mobile phase additive in the HPLC separation of the atropisomers of some N ‐arylthiazoline‐2‐thiones and N ‐arylthiazoline‐2‐ones: Attempts to quantify the effect of selected structural parameters

Author(s) -

Roussel Christian,

Favrou Anita

Publication year - 1993

Publication title -

chirality

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.43

H-Index - 77

eISSN - 1520-636X

pISSN - 0899-0042

DOI - 10.1002/chir.530050613

Subject(s) - chemistry , atropisomer , substituent , high performance liquid chromatography , chromatography , chiral column chromatography , enantiomer , chiral stationary phase , phase (matter) , cyclodextrin , organic chemistry

The effect of the position and type of the substituent on the chromatographic separation of N ‐arylthiazoline‐2‐thione and arylthiazoline‐2‐one atropisomers are described in reversed‐phase HPLC using β‐ or ‐β‐cyclodextrin as chiral mobile phase additive. A quantitative approach to experimental design has been developed. © 1993 Wiley‐Liss, Inc.

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