Detailed investigations into the Akabori-Momotani reaction for the synthesis of amphetamine type stimulants: Part 2.

[1]  Helen Salouros,et al.  Profiling ephedrine prepared from N-methylalanine via the Akabori-Momotani reaction. , 2018, Drug testing and analysis.

[2]  R. Firestone.  The Low Energy of Concert in Many Symmetry‐Allowed Cycloadditions Supports a Stepwise‐Diradical Mechanism , 2013 .

[3]  Alison Beavis,et al.  A review of impurity profiling and synthetic route of manufacture of methylamphetamine, 3,4-methylenedioxymethylamphetamine, amphetamine, dimethylamphetamine and p-methoxyamphetamine. , 2013, Forensic science international.

[4]  G. Röschenthaler,et al.  Nucleophilic properties of a nonstabilized azomethine ylide derived from sarcosine and cyclohexanone. A novel domino reaction leading to substituted 4-aryl-2-pyrrolidones , 2012 .

[5]  K. Houk,et al.  Entropy versus tether strain effects on rates of intramolecular 1,3-dipolar cycloadditions of N-alkenylnitrones , 2011 .

[6]  K. Houk,et al.  Dynamics of 1,3-dipolar cycloadditions: energy partitioning of reactants and quantitation of synchronicity. , 2010, Journal of the American Chemical Society.

[7]  G. Miskelly,et al.  Formation of Trifluoroacetylated Ephedrine During the Analysis of a Pseudoephedrine‐Formaldehyde Adduct by TFAA Derivatization Followed by GC‐MS , 2009, Journal of forensic sciences.

[8]  S. Gadre,et al.  Construction of enantiopure pyrrolidine ring system via asymmetric [3+2]-cycloaddition of azomethine ylides. , 2006, Chemical reviews.

[9]  E. Brenna,et al.  Determination of the synthetic origin of methamphetamine samples by 2H NMR spectroscopy. , 2006, Analytical chemistry.

[10]  I. Coldham,et al.  Intramolecular dipolar cycloaddition reactions of azomethine ylides. , 2005, Chemical reviews.

[11]  K. Houk,et al.  Theoretical Prediction and Experimental Tests of Conformational Switches in Transition States of Diels−Alder and 1,3-Dipolar Cycloadditions to Enol Ethers , 1998 .

[12]  S. Takenaka,et al.  Simple generation of nonstabilized azomethine ylides through decarboxylative condensation of α-amino acids with carbonyl compounds via 5-oxazolidinone intermediates , 1987 .

[13]  R. Aitken,et al.  With Azomethine Ylides , 2010 .

[14]  Y. Urano,et al.  Investigation of the origin of ephedrine and methamphetamine by stable isotope ratio mass spectrometry: a Japanese experience. , 2005, Bulletin on narcotics.

[15]  Warren J. Hehre,et al.  A Guide to Molecular Mechanics and Quantum Chemical Calculations , 2003 .

[16]  S. Akabori,et al.  On the New Reaction Giving Alcamines of Ephed-rine and Adrenaline Series , 1943 .