Chiral compounds are ubiquitous in nature and play a pivotal role in biochemical processes,
in chiroptical materials and applications, and as chiral drugs. The analysis and …

An historical review of the design of chiral stationary phases (CSPs) in the Pirkle
laboratories is presented. Beginning with the discovery of the non-equivalence of nuclear …

Stereochemistry of Organic Compounds The first fully referenced, comprehensive book on
this subject in more than thirty years, Stereochemistry of Organic Compounds contains up-to …

The dependence of the chemical or biological activity of a substance often depends upon its
stereochemistry, a fact recognized for over a century. However, accurate descriptions of the …

The study investigates the chiral recognition mechanism for the stereochemical resolution of
enantiomeric aromatic alcohols on a commercially available cellulose tribenzoate high …

Geometric considerations require that a minimum of three simultaneous interactions occur if
a chiral molecule is to “recognize” the chirality of other molecules. Moreover, chiral …

The potential of the chromatographic separation of enantiomers on a preparative scale as a
tool for the isolation of optically pure compounds is gaining increasing recognition. This …

A series of enantiomeric amides were resolve on a commercially available chiral stationary
phase (CSP0 consisting of cellulose tribenzoate coated on macroporous silica. The amides …

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 …

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 …