Literature DB >> 27604095

Laboratory-Scale Preparative Enantioseparations of Pharmaceutically Relevant Compounds on Commercially Available Chiral Stationary Phases for HPLC.

Roccaldo Sardella1, Federica Ianni1, Maura Marinozzi1, Antonio Macchiarulo1, Benedetto Natalini1.   

Abstract

In response to the outburst of research in the field of synthetic medicinal chemistry, enantioselective chromatography methods based on the use of chiral stationary phases (CSPs) found immediate acceptance as the elective choice for the analytical determinations of the enantiomeric purity of synthetic compounds. In contrast to an initial scepticism, also the preparative-scale applications are gaining increasing recognition as a powerful alternative to enantioselective synthesis for the supply of pure enantiomers of bioactive compounds. The increasing success of liquid chromatography methods has been made possible thanks to the development of highly efficient CSPs allowing the enantioresolution of practically all the chemical classes of chiral compounds. However, only few CSPs are really suitable for preparative- scale applications, being the loading capacity is the major concern for preparativescale enantioseparations. The cellulose- and amylose-based CSPs present the highest loading capacity and enantiodiscrimination power, which makes these CSPs the most versatile and applicable for preparative-scale applications in all the applicable elution modes (reversedphase, normal-phase, and with polar-organic or polar-ionic eluents). However, also other types of CSPs have been successfully employed at this regard (brush-type phases, polyacrylamide and cross-linked di-allyltartardiamide phases as well as cyclodextrin, and glycopeptide containing phases). Several instrumental methods exist for the determination of the absolute configuration of organic compounds in absence of known enantiopure reference standards. The most widely known are X-ray crystallography, followed by chirooptical methods [e.g., electronic and vibrational circular dichroism (ECD and VCD, respectively)] and nuclear magnetic resonance (NMR) spectroscopy. All these aspects will be treated in the review. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

Entities:  

Keywords:  Laboratory-scale preparative enantioresolution; absolute configuration; commercial chiral stationary phases; high-performance liquid chromatography (HPLC); pharmaceutically relevant compounds; racemiczzm321990approach

Mesh:

Substances:

Year:  2017        PMID: 27604095     DOI: 10.2174/0929867323666160907111107

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  6 in total

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Journal:  RSC Adv       Date:  2018-06-05       Impact factor: 4.036

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Review 4.  Chiral Separations in Preparative Scale: A Medicinal Chemistry Point of View.

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5.  Synthesis, resolution, and absolute configuration determination of a vicinal amino alcohol with axial chirality. Application to the synthesis of new box and pybox ligands.

Authors:  Pilar López-Ram-de-Víu; José A Gálvez; María D Díaz-de-Villegas
Journal:  Chirality       Date:  2022-05-24       Impact factor: 2.183

6.  In Vitro and In Vivo Sequestration of Phencyclidine by Me4 Cucurbit[8]uril*.

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  6 in total

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