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Pure Appl. Chem., 1993, Vol. 65, No. 6, pp. 1319-1328

doi:10.1351/pac199365061319

Stereocontrolled synthesis via chiral aziridines

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  • LI Yuling, GU Dagong, XU Xiaoping, JI Shunjun: Ring-opening of N-Tosyl Aziridines with Hydroxyl Compounds Catalyzed by Acidic Ionic Liquid. Chin J Chem 2009, 27, 1558. <doi:10.1002/cjoc.200990263>
  • Michaux Julien, Niel Gilles, Campagne Jean-Marc: Stereocontrolled routes to β,β′-disubstituted α-amino acids. Chem Soc Rev 2009, 38, 2093. <doi:10.1039/b812116h>
  • Wróblewska Agnieszka, Ławro Ewelina, Milchert Eugeniusz: Influence of process parameters on the epoxidation of 2-buten-1-ol over titanium silicalite TS-1 catalyst. Chem Pap 2008, 62, 147. <doi:10.2478/s11696-008-0004-4>
  • Janardanan Deepa, Sunoj Raghavan B.: Computational Investigations on the General Reaction Profile and Diastereoselectivity in Sulfur Ylide Promoted Aziridination. Chem Eur J 2007, 13, 4805. <doi:10.1002/chem.200700303>
  • Wang Xisheng, Ding Kuiling: One-Pot Enantioselective Aziridination of Olefins Catalyzed by a Copper(I) Complex of a Novel Diimine Ligand by Using PhI(OAc)2 and Sulfonamide as Nitrene Precursors. Chem Eur J 2006, 12, 4568. <doi:10.1002/chem.200501109>
  • Ma Linge, Du Da-Ming, Xu Jiaxi: Asymmetric aziridination of 1,3-dienes catalyzed by bisoxazoline-copper complexes. Chirality 2006, 18, 575. <doi:10.1002/chir.20282>
  • Sasaki Akira, Sunagawa Makoto: Recent advances in carbapenem chemistry (review). Chem Heterocycl Compd 1998, 34, 1249. <doi:10.1007/BF02256805>
  • Li An-Hu, Zhou Yong-Gui, Dai Li-Xin, Hou Xue-Long, Xia Li-Jun, Lin Lin: Asymmetrische Aziridinierung über Ylide: hochstereoselektive Synthese von Alkinyl-N-sulfonylaziridinen. Angew Chem 1997, 109, 1375. <doi:10.1002/ange.19971091221>