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Pure Appl. Chem., 1996, Vol. 68, No. 3, pp. 735-738

http://dx.doi.org/10.1351/pac199668030735

Aziridine and azirine carboxylic esters

Binne Zwandenburg and L. Thijs

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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>
  • Ishikawa Tsutomu: Aziridine-2-carboxylates: Preparation, Nucleophilic Ring Opening, and Ring Expansion. HETEROCYCLES 2012, 85, 2837. <http://dx.doi.org/10.3987/REV-12-748>
  • Tomasini Claudia, Angelici Gaetano, Castellucci Nicola: Foldamers Based on Oxazolidin-2-ones. Eur J Org Chem 2011, 2011, 3648. <http://dx.doi.org/10.1002/ejoc.201100493>
  • ZWANENBURG B., THIJS L.: ChemInform Abstract: Aziridine and Azirine Carboxylic Esters. ChemInform 2010, 27, no. <http://dx.doi.org/10.1002/chin.199641270>
  • Samimi Heshmat A., Mamaghani Manouchehr, Tabatabaeian Khalil: An efficient synthesis of 5-benzoyloxazolines by regio- and stereo-controlled reaction of N-substituted 2-benzoylaziridines under microwave irradiation. J Heterocyclic Chem 2008, 45, 1765. <http://dx.doi.org/10.1002/jhet.5570450632>
  • Palacios Francisco, Ochoa de Retana Ana M., Gil José I., Alonso José M.: Regioselective synthesis of 4- and 5-oxazole-phosphine oxides and -phosphonates from 2H-azirines and acyl chlorides. Tetrahedron 2004, 60, 8937. <http://dx.doi.org/10.1016/j.tet.2004.07.013>
  • 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>
  • Palacios Francisco, Aparicio Domitila, Ochoa de Retana Ana Marı́a, de los Santos Jesús M., Gil José I., López de Munain Rafael: Asymmetric synthesis of 2H-aziridine phosphonates, and α- or β-aminophosphonates from enantiomerically enriched 2H-azirines. Tet Asymm 2003, 14, 689. <http://dx.doi.org/10.1016/S0957-4166(03)00089-2>
  • 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>
  • 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>
  • Filigheddu Silvia N., Masala Simonetta, Taddei Maurizio: Solid phase synthesis of aziridine 2-carboxylates. Tetrahetron Lett 1999, 40, 6503. <http://dx.doi.org/10.1016/S0040-4039(99)01337-4>
  • Filigheddu Silvia N., Taddei Maurizio: Small ring constrained peptidomimetics. Synthesis of aziridine parallel β-sheet mimetics. Tetrahetron Lett 1998, 39, 3857. <http://dx.doi.org/10.1016/S0040-4039(98)00632-7>
  • Hruby Victor J., Li Guigen, Haskell-Luevano Carrie, Shenderovich Mark: Design of peptides, proteins, and peptidomimetics in chi space. Biopolymers (Biospectroscopy) 1997, 43, 219. <http://dx.doi.org/10.1002/(SICI)1097-0282(1997)43:3<219::AID-BIP3>3.0.CO;2-Y>