Enantiomeric separation of Novel Psychoactive Substances by capillary electrophoresis using (+)-18-crown-6-tetracarboxylic acid as chiral selector-Reference-Cited by-同舟云学术

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Enantiomeric separation of Novel Psychoactive Substances by capillary electrophoresis using (+)-18-crown-6-tetracarboxylic acid as chiral selector

Published:2018-06-19 Issue:8 Volume:30 Page:1019-1026
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Hägele Johannes S.¹,Schmid Martin G.¹^ORCID

Affiliation:

1. Department of Pharmaceutical Chemistry, Institute of Pharmaceutical Sciences; University of Graz; Graz Austria

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chir.22981/fullpdf

Reference37 articles.

1. 2017

2. Chiral separation and quantification of R/S-amphetamine, R/S-methamphetamine, R/S-MDA, R/S-MDMA, and R/S-MDEA in whole blood by GC-EI-MS;Rasmussen;J Chromatogr B Analyt Technol Biomed Life Sci,2006

3. Methamphetamine-properties and analytical methods of enantiomer determination;Jirovsky;Forensic Sci Int,1998

4. Methcathinone (‘cat’): an enantiomeric potency comparison;Glennon;Pharmacol Biochem Behav,1995

5. Direct chiral resolution of phenylalkylamines using a crown ether chiral stationary phase;Aboul-Enein;Biomed Chromatogr,1997

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