This review focuses on the evolution of Pirkle-type chiral stationary phases (CSPs), based
on chiral recognition mechanism of small molecules and applications directly related with …

A literature survey covering the report on Pirkle-type chiral stationary phases (CSPs) from
January 2000 to March 2017 is presented in this review. More than 200 CSPs comprising …

In this article, we examine the docking of 10 analytes on the Whelk-O1 stationary phase. A
proper representation of analyte flexibility is essential in the docking analysis, and analyte …

The resolution of seven enantiomeric pairs of chiral derivatives of xanthones (CDXs) on (S,
S)‐Whelk‐O1 and l‐phenylglycine chiral stationary phases (CSPs) was systematically …

A modification is proposed in Kagan's amide in order to improve its ability to offer stronger
hydrogen bonding and hence better ability to bind with substrates. Introduction of chlorine in …

Rational in silico optimization of the Whelk-O1 chiral stationary phase (CSP) has been
carried out based on the chiral recognition mechanism extracted from previous molecular …

Optically active roof-shape amines were prepared and scanned as chiral solvating agents to
study molecular recognition of acids by NMR analysis. Three types of amines were studied …

A modified Kagan's amide, N-((S)-1-(3, 5-bis (trifluoromethyl) phenyl) ethyl)-3, 5-
dinitrobenzamide [(S)-2] has been designed, synthesized and screened as a Chiral …

The Kagan's amide is used as chiral solvating agent to discriminate the signals of optically
active analytes in NMR spectroscopy. Three fluorinated derivatives of this amide are …

Dinitrodehydroabietic acid (12, 14-dinitroDHAA), a chiral acid obtained by the nitration of
optical dehydroabietic acid (DHAA), was successfully employed as resolving agent. The …