References
- Kürti L, Czako B. Strategic applications of named reactions in organic synthesis. Elsevier Academic Press; 2005.
- Palomo C, Oiarbide M, Laso A. Recent advances in the catalytic assymettric nitroaldol (Henry) reaction. Eur J Org Chem. 2007;16:2561.10.1002/(ISSN)1099-0690
- Luzzio F. The Henry reaction: recent examples. Tetrahedron. 2001;57:915.10.1016/S0040-4020(00)00965-0
- Sasai H, Suzuki T, Itoh N, Arai S, Shibasaki M. Effects of rare earth metals on the catalytic asymmetric nitroaldol reaction. Tetrahedron Lett. 1993;34:2657.10.1016/S0040-4039(00)77649-0
- McAnda AF, Roberts KD, Smallridge AJ, Ten A, Trewhella MA. Mechanism of the yeast mediated reduction of nitrostyrenes in light petroleum. J Chem Soc, Perkin Trans 1. 1998;1(3):501.10.1039/a706353i
- Palomo C, Oiarbide M, Laso A. Recent advances in the catalytic assymettric nitroaldol (Henry) reaction. Eur J Org Chem. 2007;16(2561):2007.
- Sasai H, Suzuki T, Itoh N, Shibasaki M. Catalytic asymmetric nitroaldol reactions – A new practical method for the preparation of the optically active Lanthanum complex. Tetrahedron Lett. 1993;34(5):851–854.10.1016/0040-4039(93)89030-T
- Sasai H, Suzuki T, Arai S, Arai T, Shibasaki M. Basic character of rare-earth-metal alkoxides – Utilisation in catalytic C-C bond forming reactions and catalytic asymmetric nitroaldol reactions. J Am Chem Soc. 1992;114(11):4418–4420.10.1021/ja00037a068
- Trost BM, Yeh VSC. A dinuclear Zn catalyst for the asymmetric nitroaldol (Henry) reaction. Angew Chem Int Ed. 2002;41(5):861–863.10.1002/1521-3773(20020301)41:5<861::AID-ANIE861>3.0.CO;2-V
- Christensen C, Juhl K, Jørgensen KA. Catalytic asymmetric Henry reactions – A simple approach to optically active β-nitro α–hydroxy esters. Chem Commun. 2001;21:2222–2223.10.1039/b105929g
- Kogami Y, Nakajima T, Ashizawa T, Kezuka S, Ikeno T, Yamada T. Enantioselective Henry reaction catalyzed by Salen-Cobalt complexes. Chem Lett. 2004;614–615.
- Australian Crime Commission. 2013-2014. Illicit Drug Data Report.
- Bell S. Forensic Chemistry. 2nd ed. West Virginia: Pearson Education; 2013.
- McPherson S, Hall H, Yudko E. Methamphetamine use: Clinical and forensic aspects. 2nd ed. CRC Press; 2008. p. 17–18.
- Lee J, Han E, Lee S, Kim E, Park Y, Lim M, Chung H, Park J. Analysis of the impurities in the methamphetamine synthesized by three different methods from ephedrine and pseudoephedrine. Forensic Sci Int. 2006;161:209.10.1016/j.forsciint.2006.02.054
- Bremer N, Woolery R. The yield of methamphetamine, unreacted precursor and Birch By-Product with the Lithium-Ammonia reduction Method as employed in Clandestine Laboratories. MAFS Newsletter. 1999.
- McMurry J. Organic Chemistry. 7th ed. Thomson - Brooks/Cole; 2008.
- Person E, Meyer J, Vyvyan J. Structural determination of the principal byproduct of the lithium-ammonia reduction method of methamphetamine manufacture. J Forensic Sci. 2005;50:1.10.1520/JFS2004204
- Covey H. The methamphetamine crisis: strategies to save addicts, families, and communities. Greenwood Publishing Group. 2007. p. 20–22.
- Windahl K, McTigue M, Pearson J, Pratt S, Rowe J, Sear E. Investigation of the impurities found in methamphetamine synthesised from pseudoephedrine by reduction with hydriodic acid and red phosphorus. Forensic Sci Int. 1995;76:97.10.1016/0379-0738(95)01803-4
- McAnda AF, Roberts KD, Smallridge AJ, Ten A, Trewhella MA. Mechanism of the yeast mediated reduction of nitrostyrenes in light petroleum. J Chem Soc, Perkin Trans 1. 1998;3:501.