Literature DB >> 28168709

Recent trends and applications in liquid-phase chromatography enantioseparation of atropisomers.

Paola Peluso1, Victor Mamane2, Emmanuel Aubert3, Sergio Cossu4.   

Abstract

The term Atropisomerism defines a type of enantiomerism that arises from hindered rotation around an axis that makes two rotational isomers enantiomers. Atropisomeric compounds are present in nature, being important building blocks of many biologically active compounds. Atropisomers have been extensively studied in environmental and toxicological chemistry and, in particular, separating them has become a need in specific fields as organic synthesis and pharmaceutical research. High-performance LC has been fruitfully applied in this context, and despite HPLC separation on chiral stationary phase is considered as mature technology nowadays, in the last years several advancements and applications contributed to study compounds where axial chirality is of utmost importance. Moreover, dynamic chromatography has been exploited as a versatile tool for kinetic studies of systems with slow internal motion gaining essential information on their stereodynamic behavior. On this basis, current topics and trends in liquid-phase chromatography enantioseparation of atropisomers are presented herein with specific focus on new representative applications with HPLC, covering years 2010-2016. Some examples concerning supercritical fluid chromatography applications are also reported. This review aims to provide the reader with a modern overview of the field to highlight the renewed interest toward the chemistry of molecules with atropisomeric properties. A systematic compilation of all published literature has not been attempted.
© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Keywords:  Atropisomerism; Chiral stationary phase; Dynamic chromatography; Enantioseparation; HPLC

Mesh:

Year:  2017        PMID: 28168709     DOI: 10.1002/elps.201600502

Source DB:  PubMed          Journal:  Electrophoresis        ISSN: 0173-0835            Impact factor:   3.535


  2 in total

1.  Enantioselective Synthesis of Pyrrolopyrimidine Scaffolds through Cation-Directed Nucleophilic Aromatic Substitution.

Authors:  Mariel M Cardenas; Sean T Toenjes; Christopher J Nalbandian; Jeffrey L Gustafson
Journal:  Org Lett       Date:  2018-03-21       Impact factor: 6.005

2.  Chiral Chalcogen Bond Donors Based on the 4,4'-Bipyridine Scaffold.

Authors:  Robin Weiss; Emmanuel Aubert; Paola Peluso; Sergio Cossu; Patrick Pale; Victor Mamane
Journal:  Molecules       Date:  2019-12-06       Impact factor: 4.411

  2 in total

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