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Synthetic reductions in clandestine amphetamine and methamphetamine laboratories: A review
TL;DR: A review of synthetic reductions utilized in the clandestine manufacture of amphetamine and methamphetamine is presented in this article, where general discussions on the mechanism of heterogeneous catalysis, dissolving metals, hydrides and non-metal reductions used in the manufacture of methamphetamines with over 80 references are presented.
Journal ArticleDOI
An Evaluation of the Potential for Clandestine Manufacture of 3,4-Methylenedioxyamphetamine (MDA) Analogs and Homologs
TL;DR: In this paper, a predictive scheme for 3,4-Methylenedioxyamphetamine (MDA) analogs is presented based on putative Central Nervous System activity, existence or formulation of a reasonable synthesis method, and availability of the required precursors.
Journal ArticleDOI
Metabolic N-Oxidation of Primary and Secondary Aliphatic Medicinal Amines
R. T. Coutts,A. H. Beckett +1 more
TL;DR: In this paper, the authors describe the metabolic n-oxidation of primary and secondary aliphatic medicinal Amines, and present a detailed review of the results of their experiments.
Journal ArticleDOI
Synthesis of deuterio-l-amphetamine, d1 sulfate.
TL;DR: In vitro metabolism studies indicate that a significant deuterium isotope effect operates in the oxidative deamination of deuterio-l-amphetamine.
Journal ArticleDOI
Cytochrome P-455 nm complex formation in the metabolism of phenylalkylamines. XII. Enantioselectivity and temperature dependence in microsomes and reconstituted cytochrome P-450 systems from rat liver.
TL;DR: In this article, the enantiomers of amphetamine, 1-phenyl-2-pentanamine, N-hydroxyamphetamine, and 2-nitroso-1-propane were studied with three different enzyme systems.