Enantiomeric separation of new cathinone derivatives designer drugs by capillary electrochromatography using a chiral stationary phase, based on amylosetris(5-chloro-2-methylphenylcarbamate)-Reference-Cited by-同舟云学术

Enantiomeric separation of new cathinone derivatives designer drugs by capillary electrochromatography using a chiral stationary phase, based on amylosetris(5-chloro-2-methylphenylcarbamate)

Published:2014-07-14 Issue:21-22 Volume:35 Page:3242-3249
ISSN:0173-0835
Container-title:ELECTROPHORESIS
language:en
Short-container-title:ELECTROPHORESIS

Author:

Aturki Zeineb¹,Schmid Martin G.²,Chankvetadze Bezhan³,Fanali Salvatore¹

Affiliation:

1. Institute of Chemical Methodologies; Italian National Research Council; Monterotondo Rome Italy

2. Department of Pharmaceutical Chemistry; Institute of Pharmaceutical Sciences; Karl-Franzens-University Graz; Graz Austria

3. Institute of Physical and Analytical Chemistry; School of Exact and Natural Sciences; Tbilisi State University; Tbilisi Georgia

Publisher

Wiley

Subject

Clinical Biochemistry,Biochemistry,Analytical Chemistry

Reference46 articles.

1. Cathinone derivatives: A review of their chemistry, pharmacology and toxicology

2. Designer cathinones—An emerging class of novel recreational drugs

3. Bath salts and synthetic cathinones: An emerging designer drug phenomenon

4. Clinical experience with and analytical confirmation of “bath salts” and “legal highs” (synthetic cathinones) in the United States

5. Methcathinone (“cat”): An enantiomeric potency comparison

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