Please use this identifier to cite or link to this item: http://hdl.handle.net/10995/27152
Title: Identification and analytical properties of new synthetic cannabimimetics bearing 2,2,3,3-tetramethylcyclopropanecarbonyl moiety
Authors: Shevyrin, V.
Melkozerov, V.
Nevero, A.
Eltsov, O.
Morzherin, Y.
Shafran, Y.
Issue Date: 2013
Citation: Identification and analytical properties of new synthetic cannabimimetics bearing 2,2,3,3-tetramethylcyclopropanecarbonyl moiety / V. Shevyrin, V. Melkozerov, A. Nevero [et al.] // Forensic Science International. — 2013. — Vol. 226. — № 1-3. — P. 62-73.
Abstract: By means of gas chromatography with mass spectrometry detector (GC-MS), liquid chromatography-mass spectrometry (LC-MS) and nuclear magnetic resonance spectroscopy (NMR), structure of a series from a novel class of synthetic cannabimimetics bearing 2,2,3,3-tetramethylcyclopropanecarbonyl moiety was established. It was found that this fragment could undergo thermal ring-opening into isomeric structures. The title compounds under action of hydrochloric acid can transform into new compounds which structure is discussed in the paper. The compounds identified could be referred to a new class of 'designer drugs' and are in illegal turnover in Russia and Belarus since the summer of 2011. Analytical data obtained in the paper will make possible reliable identification of such new 'designer drugs' during forensic examination. © 2012 Elsevier Ireland Ltd.
Keywords: (1H-INDOL-3-YL)(2,2,3,3-TETRAMETHYLCYCLOPROPYL)METHANONE DERIVATIVES
A-836,339
CANNABIMIMETICS
DESIGNER DRUGS
GC-MS
LC-MS
NMR
(2,2,3,3 TETRAMETHYLCYCLOPROPYL)METHANONE DERIVATIVE
CANNABIMIMETIC AGENT
DESIGNER DRUG
UNCLASSIFIED DRUG
ARTICLE
CHEMICAL STRUCTURE
FORENSIC SCIENCE
GAS CHROMATOGRAPHY
ISOMER
LIQUID CHROMATOGRAPHY
MASS SPECTROMETRY
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY
PRIORITY JOURNAL
RING OPENING
URI: http://hdl.handle.net/10995/27152
SCOPUS ID: 84875593538
ISSN: 0379-0738
DOI: 10.1016/j.forsciint.2012.12.009
Appears in Collections:Научные публикации, проиндексированные в SCOPUS и WoS CC

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