Chiral Resolution and Absolute Configuration of the Enantiomers of the Psychoactive “Designer Drug” 3,4-Methylenedioxypyrovalerone-Reference-Cited by-同舟云学术

Chiral Resolution and Absolute Configuration of the Enantiomers of the Psychoactive “Designer Drug” 3,4-Methylenedioxypyrovalerone

Published:2015-02-26 Issue:4 Volume:27 Page:287-293
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Suzuki Masaki¹,Deschamps Jeffrey R.²,Jacobson Arthur E.¹,Rice Kenner C.¹

Affiliation:

1. Drug Design and Synthesis Section, Molecular Targets and Medications Discovery Branch, National Institute on Drug Abuse, National Institutes of Health; Department of Health and Human Services; Bethesda Maryland

2. Center for Biomolecular Science and Engineering; Naval Research Laboratory; Washington, D.C.

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chir.22423/fullpdf

Reference11 articles.

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3. Clinical experience with and analytical confirmation of “bath salts” and “legal highs” (synthetic cathinones) in the United States;Spiller;Clin Toxicol,2011

4. Bath salts and synthetic cathinones: An emerging designer drug phenomenon;German;Life Sci,2014

5. Synthetic cathinones: “A khat and mouse game.”;Katz;Toxicol Lett,2014

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