Pure and Applied Chemistry

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• Samimi Heshmat A., Yamin Bohari M., Soltani Marzieh: Regio- and stereo-controlled isomerization of 1,2-diaroyl-3-aryl aziridines to the corresponding N-((Z)-1-oxo-1,3-diphenylprop-2-en-2-yl) benzamide. J IRAN CHEM SOC 2014. <http://dx.doi.org/10.1007/s13738-014-0416-8>
• Kavanagh Sarah A., Piccinini Alessandro, Connon Stephen J.: The asymmetric synthesis of terminal aziridines by methylene transfer from sulfonium ylides to imines. Org. Biomol. Chem. 2013, 11, 3535. <http://dx.doi.org/10.1039/c3ob27271k>
• Zwanenburg Binne: ChemInform Abstract: Synthetic Potential of Heteroatomic Ring Systems. ChemInform 2010, 30, no. <http://dx.doi.org/10.1002/chin.199952279>
• Ajish Kumar K. S., Chaudhari Vinod D., Dhavale Dilip D.: Efficient synthesis of (+)-1,8,8a-tri-epi-swainsonine, (+)-1,2-di-epi-lentiginosine, (+)-9a-epi-homocastanospermine and (−)-9-deoxy-9a-epi-homocastanospermine from a d-glucose-derived aziridine carboxylate, and study of their glycosidase inhibitory activities. Org Biomol Chem 2008, 6, 703. <http://dx.doi.org/10.1039/b712753g>
• Ghorai Manas K., Ghosh Koena, Das Kalpataru: Copper(II) triflate promoted cycloaddition of α-alkyl or aryl substituted N-tosylaziridines with nitriles: a highly efficient synthesis of substituted imidazolines. Tetrahetron Lett 2006, 47, 5399. <http://dx.doi.org/10.1016/j.tetlet.2006.05.059>
• Bitar Yaser, Degel Björn, Schirmeister Tanja, Holzgrabe Ulrike: Comparison of the separation of aziridine isomers applyingheptakis(2,3-di-O-methyl-6-sulfato)β-CD andheptakis(2,3-di-O-acetyl-6-sulfato)β-CD in aqueous and nonaqueous systems. Eletrophoresis 2005, 26, 3897. <http://dx.doi.org/10.1002/elps.200500176>
• Dhavale Dilip D., Kumar K. S. Ajish, Chaudhari Vinod D., Sharma Tarun, Sabharwal Sushma G., PrakashaReddy J.: Aziridine carboxylate from d-glucose: synthesis of polyhydroxylated piperidine, pyrrolidine alkaloids and study of their glycosidase inhibition. Org Biomol Chem 2005, 3, 3720. <http://dx.doi.org/10.1039/b509216g>
• Righi Giuliana, Ciambrone Simona: Stereocontrolled addition of boron enolates to trans α,β-aziridine aldehydes. A new route to anti-1,2-amino alcohols. Tetrahetron Lett 2004, 45, 2103. <http://dx.doi.org/10.1016/j.tetlet.2004.01.059>
• Righi Giuliana, Catullo Simona: 2,3‐Bifunctionalized Aziridines: Regioselective MgBr₂‐Mediated Opening Under “Chelation Controlled” Conditions. Synth Common 2004, 34, 85. <http://dx.doi.org/10.1081/SCC-120027242>
• Bonini Bianca F., Fochi Mariafrancesca, Comes-Franchini Mauro, Ricci Alfredo, Thijs Lambertus, Zwanenburg Binne: Synthesis of ferrocenyl-oxazolines by ring expansion of N-ferrocenoyl-aziridine-2-carboxylic esters. Tet Asymm 2003, 14, 3321. <http://dx.doi.org/10.1016/j.tetasy.2003.08.001>
• Kroutil Jiří, Karban Jindřich, Trnka Tomáš, Buděšínský Miloš, Černý Miloslav: Preparation of O-, S- and N-Benzyl Derivatives of 1,6-Anhydro-β-D-hexopyranoses via Aziridine Ring Opening. Collect Czech Chem Commun 2002, 67, 1805. <http://dx.doi.org/10.1135/cccc20021805>
• Ali Dondas H, Cummins Jonathan E, Grigg Ronald, Thornton-Pett Mark: X=Y–ZH Systems as potential 1,3-dipoles. Part 53: Sequential nucleophilic ring opening-1,3-dipolar cycloaddition reactions of Z-oxime anions with aziridines and dipolarophiles. Tetrahedron 2001, 57, 7951. <http://dx.doi.org/10.1016/S0040-4020(01)00767-0>
• Aggarwal Varinder K, Stenson Rachel A, Jones Ray V.H, Fieldhouse Robin, Blacker John: A novel procedure for the synthesis of aziridines: application of Simmons–Smith reagents to aziridination. Tetrahetron Lett 2001, 42, 1587. <http://dx.doi.org/10.1016/S0040-4039(00)02310-8>
• Hermsen P.J, Cremers J.G.O, Thijs L, Zwanenburg B: Enantioselective diethylzinc addition to aldehydes using azetidine-derived chiral catalysts. Tetrahetron Lett 2001, 42, 4243. <http://dx.doi.org/10.1016/S0040-4039(01)00659-1>