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Pure Appl. Chem., 1990, Vol. 62, No. 7, pp. 1405-1408

http://dx.doi.org/10.1351/pac199062071405

A few new methods for asymmetric synthesis

S. Itô and T. Tsunoda

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  • den Hartog Tim, Maciá Beatriz, Minnaard Adriaan J., Feringa Ben L.: Copper-Catalyzed Asymmetric Allylic Alkylation of Halocrotonates: Efficient Synthesis of Versatile Chiral Multifunctional Building Blocks. Adv Synth Catal 2010, 352, 999. <http://dx.doi.org/10.1002/adsc.201000109>
  • ITÔ Shô: Development of New Synthetic Reagents in Mitsunobu-Type Reaction. YAKUGAKU ZASSHI 2001, 121, 567. <http://dx.doi.org/10.1248/yakushi.121.567>
  • Suh Young-Ger, Lee Jee-Yeon, Kim Soon-Ai, Jung Jae-Kyong: A New Ring Expansion Reaction of 1-Acyl-2-vinylpiperidine and 1-Acyl-2-Vinylpiperazine via Aza-Claisen Rearrangement of Amide Enolate. Synth Common 1996, 26, 1675. <http://dx.doi.org/10.1080/00397919608002605>
  • Ozegowski Rüdiger, Kunath Annamarie, Schick Hans: The different behaviour of syn- and anti-2,3-dimethylbutanedioic anhydride in the lipase-catalyzed enantioselective alcoholysis. Tet Asymm 1995, 6, 1191. <http://dx.doi.org/10.1016/0957-4166(95)00145-F>
  • Cook Ggregory R., Stille John R.: Stereochemical consequences of the lewis acid-promoted 3-aza-cope rearrangement of N-alkyl-N-allyl enamines. Tetrahedron 1994, 50, 4105. <http://dx.doi.org/10.1016/S0040-4020(01)86707-7>
  • Tsunoda Tetsuto, Tatsuki Shinji, Kataoka Kazuko, Itô Shô: A Stereoselective Synthesis of(-)-Isoiridomyrmecin. Application of the Asymmetric Aza-Claisen Rearrangement. Chem Lett 1994, 543. <http://dx.doi.org/10.1246/cl.1994.543>
  • Cid Maria Magdalena, Pombo-Villar Esteban: Enantioselective Synthesis of 3- Azabicyclo[4.3.0]nonane Alkaloids. HCA 1993, 76, 1591. <http://dx.doi.org/10.1002/hlca.19930760416>
  • Ager David J., East Michael B.: The synthesis of carbohydrate derivatives from acyclic precursors. Tetrahedron 1993, 49, 5683. <http://dx.doi.org/10.1016/S0040-4020(01)87942-4>
  • Tsunoda Tetsuto, Tatsuki Shinji, Shiraishi Yoko, Akasaka Masumi, Itô Shô: Asymmetric aza-Claisen rearrangement of glycolamide and glycinamide enolates. Synthesis of optically active α-hydroxy and α-amino acids. Tetrahetron Lett 1993, 34, 3297. <http://dx.doi.org/10.1016/S0040-4039(00)73687-2>
  • Tsunoda Tetsuto, Sakai Mika, Sasaki Osamu, Sako Yoshie, Hondo Yuka, Itô Shô: Asymmetric Induction in Aza-Claisen Rearrangement of Carboxamide Enolates. Effect of Chiral Auxiliary on Nitrogen. Tetrahetron Lett 1992, 33, 1651. <http://dx.doi.org/10.1016/S0040-4039(00)91698-8>
  • Tsunoda Tetsuto, Sasaki Osamu, Takeuchi Osamu, Itô Shô: An efficient method for hydrolysis of N-monosubstituted amides utilization of intramolecular NO acyl migration in hydroxypivalimides. Tetrahedron 1991, 47, 3925. <http://dx.doi.org/10.1016/S0040-4020(01)86433-4>