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Enantiomeric .alpha.-aminopropiophenones (cathinone): preparation and investigation
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Enantioselective Synthesis of Vicinal Amino Alcohols by Oxa‐Michael Addition of (−)‐N‐Formylnorephedrine to Nitroalkenes
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ChemInform Abstract: ENANTIOMERIC α‐AMINOPROPIOPHENONES (CATHINONE): PREPARATION AND INVESTIGATION
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Synthese und Strukturaufklärung von Merucathin und Pseudomerucathin. Zwei Inhaltstoffe von Catha edulis F ORSK
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Socio-Economic Poisons: Khat, The Natural Amphetamine
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High-performance liquid chromatographic determination of (−)-cathinone in plasma
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Detection and elimination profile of cathinone in equine after norephedrine (Propalin®) administration using a validated liquid chromatography–tandem mass spectrometry method
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Recently abused β-keto derivatives of 3,4-methylenedioxyphenylalkylamines: a review of their metabolisms and toxicological analysis
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The releasing effect of the isomers of the alkaloid cathinone at central and peripheral catecholamine storage sites
inferred← citeshttps://doi.org/10.1016/0031-9422(86)80102-9openalex-snapshot
(-)-N-formylnorephedrine from Catha edulis
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An efficient synthesis of both enantiomers of Cathinone by regioselective reductive ring opening of substituted aziridines
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Clastogenic evaluation of cathinone and amphetamine in somatic cells of mice
inferred← citeshttps://doi.org/10.1016/0300-483x(90)90145-7openalex-snapshot
An evaluation of the male reproductive toxicity of cathinone
inferred← citeshttps://doi.org/10.1016/0379-0738(93)90249-aopenalex-snapshot
Gas chromatographic-mass spectrometric identification of chiral derivatives of the alkaloids of KHAT
inferred← citeshttps://doi.org/10.1016/0379-0738(94)01669-0openalex-snapshot
Chiral identification and determination of ephedrine, pseudoephedrine, methamphetamine and metecathinone by gas chromatography and nuclear magnetic resonance
inferred← citeshttps://doi.org/10.1016/b978-0-12-417302-6.00016-7openalex-snapshot
Alkaloids Derived from a C6–C1 Unit
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Forensic implications of novel synthesis of cathinone derivatives by Neber and modified Neber rearrangements
inferred← citeshttps://doi.org/10.1016/j.forsciint.2009.12.002openalex-snapshot
Cathinone preservation in khat evidence via drying
inferred← citeshttps://doi.org/10.1016/j.forsciint.2014.06.020openalex-snapshot
Proactive forensic science: A novel class of cathinone precursors
inferred← citeshttps://doi.org/10.1016/j.forsciint.2016.06.034openalex-snapshot
Identification and derivatization of selected cathinones by spectroscopic studies
inferred← citeshttps://doi.org/10.1016/j.lfs.2013.09.026openalex-snapshot
Emergence and properties of spice and bath salts: A medicinal chemistry perspective
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2-Amino ketones from osmium-catalysed oxidations of alkenes
inferred← citeshttps://doi.org/10.1016/j.molstruc.2011.06.030openalex-snapshot
X-ray structures and computational studies of several cathinones
inferred← citeshttps://doi.org/10.1016/s0021-9673(01)95394-4openalex-snapshot
Resolution of norephedrine as its 2-oxazolidone derivative: enantiomeric separation on a chiral high-performance liquid chromatographic stationary phase and preparative regeneration of the resolved isomers
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NMR Spectroscopy in Forensic Science
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Chapter 4 Alkaloids of Khat (Catha Edulis)
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Chapter 1 Forensic Chemistry of Alkaloids by Chromatographic Analysis
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The characterization of some 3,4-methylenedioxycathinone (MDCATH) homologs
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A two-step method for the preparation of homochiral cathinones
inferred← citeshttps://doi.org/10.1039/c5ob01306bopenalex-snapshot
Isolation and structural determination of non-racemic tertiary cathinone derivatives
inferred← citeshttps://doi.org/10.1080/00387019208018219openalex-snapshot
NMR Studies of Drugs. Enantiomeric Excess Determination ofN-acetylcathinone with Eu(HFC)3
inferred← citeshttps://doi.org/10.1080/10610278.2018.1444764openalex-snapshot
A joint QM/MD study on α-, β- and γ-cyclodextrins in selective complexation with cathinone
inferred← citeshttps://doi.org/10.1081/jlc-120037363openalex-snapshot
Liquid Chromatographic Resolution of Aryl α‐Amino Ketones on Chiral Stationary Phases Based on (+)‐(18‐Crown‐6)‐2,3,11,12‐Tetracarboxylic Acid
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Thermal Degradation of Synthetic Cathinones: Implications for Forensic Toxicology
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Stability of Synthetic Cathinones in Blood
inferred← citeshttps://doi.org/10.1111/j.2042-7158.1986.tb04571.xopenalex-snapshot
Metabolism of cathinone to (−)-norephedrine and (−)-norpseudoephedrine
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Estudos in silico do comportamento de catinonas sintéticas com interesse forense
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Analytical Challenges for Identification of New Psychoactive Substances: A Literature-Based Study for Seized Drugs
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Studies on (-)-Cathinone Formation in Micropropagated Plants and Tissue Cultures of Catha edulis (Khat)
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From Psychoactivity to Antimicrobial Agents: Multifaceted Applications of Synthetic Cathinones and Catha edulis Extracts
inferred← citeshttps://doi.org/10.3724/sp.j.1123.2023.03009openalex-snapshot
Rapid extraction and detection of five alkaloids in dried khat by solvent extraction-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry
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A New Approach to the Synthesis of Optically Active Norephedrine, Norpseudoephedrine and Cathinone via Double Asymmetric Induction
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