Synthesis of deuterium‐labelled standards of (±)‐DOM and (±)‐MMDA
Ajam C. Shaikh, Yu Yun Wang, Chinpiao Chen
Journal of Labelled Compounds and Radiopharmaceuticals June 1, 2007 DOI: 10.1002/jlcr.1378 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Method development Peer reviewed |
|---|---|
| Citations | 9 |
| Key points | Deuterium-labeled DOM and MMDA were synthesized for potential use as internal standards in GC-MS assays. |
Abstract
AbstractThis study describes the synthesis of deuterium‐labelled (±)‐4‐methyl‐2,5‐dimethoxyamphetamine (DOM) and (±)‐1‐(7‐methoxy‐1,3‐benzodioxol‐5‐yl)propan‐2‐amine (MMDA). The isotopically labelled compounds are potentially used as internal standards in gas chromatography–mass spectrometry (GC–MS) assays. Copyright © 2007 John Wiley & Sons, Ltd.
Citations in the library
Cites 4
- Synthesis of deuterium labeled standards of 5‐methoxy‐N,N‐dimethyltryptamine (5‐Meo‐DMT) Journal of Labelled Compounds and Radiopharmaceuticals August 14, 2006
- Phenylalkylamines with potential psychotherapeutic utility. 2. Nuclear substituted 2-amino-1-phenylbutanes Journal of Medicinal Chemistry February 1, 1980
- Substituent branching in phenethylamine-type hallucinogens: a comparison of 1-[2,5-dimethoxy-4-(2-butyl)phenyl]-2-aminopropane and 1-[2,5-dimethoxy-4-(2-methylpropyl)phenyl]-2-aminopropane. Journal of Medicinal Chemistry June 1984
- The Synthesis of Four Possible in vitro Metabolites of the Hallucinogen 1-(2,5-Dimethoxy-4-methylphenyl)-2-aminopropane (DOM) Canadian Journal of Chemistry February 1, 1974