Rodriguez, WR; Allred, RA. Synthesis of trans-4-methylaminorex from norephedrine and potassium cyanate. Microgram J., 1 Jul 2005, 3 (3–4), 154–165. 559 kB. MS,NMR,IR
Brandt, SD; Baumann, MH; Partilla, JS; Kavanagh, PV; Power, JD; Talbot, B; Twamley, B; Mahony, O; O’Brien, J; Elliott, SP; Archer, RP; Patrick, J; Singh, K; Dempster, NM; Cosbey, SH. Characterization of a novel and potentially lethal designer drug (±)-cis-para-methyl-4-methylaminorex (4,4′-DMAR, or ‘Serotoni’). Drug Test. Anal., 1 Jul 2014, 6 (7-8), 684-695. 1.1 MB. https://doi.org/10.1002/dta.1668
McLaughlin, G; Morris, N; Kavanagh, PV; Power, JD; Twamley, B; O’Brien, J; Talbot, B; Dowling, G; Mahony, O; Brandt, SD; Patrick, J; Archer, RP; Partilla, JS; Baumann, MH. Synthesis, characterization, and monoamine transporter activity of the new psychoactive substance 3′,4′-methylenedioxy-4-methylaminorex (MDMAR). Drug Test. Anal., 1 Jul 2015, 7 (7), 555-564. 517 kB. https://doi.org/10.1002/dta.1732
Klein, RFX; Sperling, AR; Cooper, DA; Kram, TC. The stereoisomers of 4-methylaminorex. J. Forensic Sci., 1 Jul 1989, 34 (4), 962–979. 455 kB. https://doi.org/10.1520/JFS12723J #4-Methylaminorex GC,MS,NMR,IR,TLC,other
Brewster, ME; Davis, FT. Appearance of aminorex as a designer analog of methylaminorex. J. Forensic Sci., 1 Mar 1991, 36 (2), 587–592. 302 kB. https://doi.org/10.1520/JFS13063J #Methylaminorex MS,NMR,other
Maier, J; Mayer, FP; Brandt, SD; Sitte, HH. DARK classics in chemical neuroscience: Aminorex analogues. ACS Chem. Neurosci., 17 Oct 2018, 9 (10), 2484–2502. 1.8 MB. https://doi.org/10.1021/acschemneuro.8b00415 #4-Methylaminorex
EMCDDA. Report on the risk assessment of 4,4′-DMAR, European Monitoring Centre for Drugs and Drug Addiction, Lisbon, 1 Oct 2015. 1.1 MB. #cis-4-MAR MS,NMR
Nichols, DE. CNS Stimulants. In Burger's Medicinal Chemistry and Drug Discovery; Abraham, DJ, Ed., John Wiley & Sons, Inc., 29 Jan 2010; pp 89–120. 1.8 MB. https://doi.org/10.1002/0471266949.bmc243 #25
Davis, FT; Brewster, ME. A fatality involving U4Euh, a cyclic derivative of phenylpropanolamine. J. Forensic Sci., 1 Mar 1988, 33 (2), 549–553. 297 kB. https://doi.org/10.1520/JFS11971J #U4Euh MS,NMR,IR,UV
Rickli, A; Kolaczynska, K; Hoener, MC; Liechti, ME. Pharmacological characterization of the aminorex analogs 4-MAR, 4,4′-DMAR, and 3,4-DMAR. Neurotoxicology, 1 May 2019, 72, 95–100. 728 kB. https://doi.org/10.1016/j.neuro.2019.02.011 #4-MAR
Bork, W; Dahlenburg, R; Gimbel, M; Jacobsen-Bauer, A; Zörntlein, S. Herleitung Von Grenzwerten Der „nicht Geringen Menge“ Im Sinne Des Btmg. Toxichem Krimtech, 1 Jan 2019, 86 (1), 5–91. 4.4 MB. #AP-002
Carson, JR; Poos, GI; Almond, HR. 2-Amino-5-aryl-2-oxazolines. Tautomerism, stereochemistry, and an unusual reaction. J. Org. Chem., 1 Jul 1965, 30 (7), 2225–2228. 535 kB. https://doi.org/10.1021/jo01018a026 #VIa other