Pure and Applied Chemistry

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• Sax Michael, Wünsch Bernhard: Solid-Phase Organic Synthesis of Dexoxadrol Analogues. Aust. J. Chem. 2013, 66, 93. <http://dx.doi.org/10.1071/CH12356>
• Siman Peter, Blatt Ofrah, Moyal Tal, Danieli Tsafi, Lebendiker Mario, Lashuel Hilal A., Friedler Assaf, Brik Ashraf: Chemical Synthesis and Expression of the HIV-1 Rev Protein. Chem Eur J of Chem Bio 2011, 12, 1097. <http://dx.doi.org/10.1002/cbic.201100033>
• Stowe G. Neil, Vendruscolo Leandro F., Edwards Scott, Schlosburg Joel E., Misra Kaushik K., Schulteis Gery, Mayorov Alexander V., Zakhari Joseph S., Koob George F., Janda Kim D.: A Vaccine Strategy that Induces Protective Immunity against Heroin. J Med Chem 2011, 54, 5195. <http://dx.doi.org/10.1021/jm200461m>
• D’Souza Malcolm John, Shuman Kevin Edward, Omondi Arnold Ochieng, Kevill Dennis Neil: Detailed analysis for the solvolysis of isopropenyl chloroformate. Eur J Chem 2011, 2, 130. <http://dx.doi.org/10.5155/eurjchem.2.2.130-135.405>
• Bettati Michela, Cavanni Paolo, Di Fabio Romano, Oliosi Beatrice, Perini Ornella, Scheid Gunther, Tedesco Giovanna, Zonzini Laura, Micheli Fabrizio: Oxa-azaspiro Derivatives: a Novel Class of Triple Re-uptake Inhibitors. ChemMedChem 2010, 5, 361. <http://dx.doi.org/10.1002/cmdc.200900482>
• Balssa Frédéric, Bonnaire Yves: Syntheses of deuterium labelled atropine and scopolamine. J Labelled Cpd Radiopharm 2009, 52, 269. <http://dx.doi.org/10.1002/jlcr.1593>
• Kharul Rajendra K., Goswami Amitgiri, Gite Archana, Godha Atul K., Jain Mukul, Patel Pankaj R.: Convenient Synthesis of Structurally Novel 1,3‐Disubstituted Azetidine Derivatives. Synth Comm 2008, 38, 1703. <http://dx.doi.org/10.1080/00397910801982340>
• Stachulski Andrew V, Scheinmann Feodor, Ferguson John R, Law Jayne L, Lumbard Keith W, Hopkins Peter, Patel Naina, Clarke Simon, Gloyne Anna, Joel Simon P: Structure–activity relationships of some opiate glycosides. Biorg Med Chem Lett 2003, 13, 1207. <http://dx.doi.org/10.1016/S0960-894X(03)00056-8>
• Flosser David A., Olofson Roy A.: Improved Synthesis of Dialkylaminopyrrolines. Synth Common 2003, 33, 2045. <http://dx.doi.org/10.1081/SCC-120021030>
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• Hirokawa Yoshimi, Harada Hiroshi, Yoshikawa Takashi, Yoshida Naoyuki, Kato Shiro: Synthesis and Structure–Activity Relationships of 4-Amino-5-chloro-N-(1,4-dialkylhexahydro-1,4-diazepin-6-yl)-2-methoxybenzamide Derivatives, Novel and Potent Serotonin 5-HT3 and Dopamine D2 Receptors Dual Antagonist. Chem Pharm Bull 2002, 50, 941. <http://dx.doi.org/10.1248/cpb.50.941>
• Senet Jean-Pierre: Phosgene chemistry and environment, recent advances clear the way to clean processes: a review. Comptes Rendus de l Académie des Sciences - Series IIC - Chemistry 2000, 3, 505. <http://dx.doi.org/10.1016/S1387-1609(00)00145-6>
• Fröhlich Karin, Wagemann Rolf, Vilsmaier Elmar: Dealkylation of N(3)-methyl-6-amino-3-azabicyclo[3.1.0]hexane derivatives. Tetrahedron 1998, 54, 13115. <http://dx.doi.org/10.1016/S0040-4020(98)00794-7>
• Guibé François: Allylic protecting groups and their use in a complex environment part I: Allylic protection of alcohols. Tetrahedron 1997, 53, 13509. <http://dx.doi.org/10.1016/S0040-4020(97)00524-3>
• Patonay Tamás, Patonay-Péli Erzsébet, Zolnai László, Mogyoródi Ferenc: α-Haloalkyl Haloformates and Related Compounds 3.¹ A Facile Synthesis of Symmetrical and Unsymmetrical Ureas via Chloromethyl Carbamates. Synth Common 1996, 26, 4253. <http://dx.doi.org/10.1080/00397919608004663>
• Ferguson John R., Lumbard Keith W., Scheinmann Feodor, Stachulski Andrew V., Stjernlöf Peter, Sundell Staffan: Efficient new syntheses of (+)- and (-)-anatoxin-a. Revised configuration of resolved 9-methyl-9-azabicyclo[4.2.1]nonan-2-one. Tetrahetron Lett 1995, 36, 8867. <http://dx.doi.org/10.1016/0040-4039(95)01842-6>
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