Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1959, 24, 3596-3600

Einwirkung des Grignard-reagenz auf die amidgruppe XXV. Darstellung von 1-methyl-2-allylpiperidin

R. Lukeš and M. Černý

Crossref Cited-by Linking

  • Amat Mercedes, Semak Vladislav, Escolano Carmen, Molins Elies, Bosch Joan: Enantioselective, protecting group-free synthesis of 1S-ethyl-4-substituted quinolizidines. Org. Biomol. Chem. 2012, 10, 6866. <>
  • Meng Wei-Hua, Wu Tian-Jun, Zhang Hong-Kui, Huang Pei-Qiang: Asymmetric syntheses of protected (2S,3S,4S)-3-hydroxy-4-methylproline and 4′-tert-butoxyamido-2′-deoxythymidine. Tetrahedron: Asymmetry 2004, 15, 3899. <>
  • Liu Liang-Xian, Ruan Yuan-Ping, Guo Zheng-Qing, Huang Pei-Qiang: A General Approach to (5S,6R)-6-Alkyl-5-benzyloxy-2-piperidinones:  Application to the Asymmetric Syntheses of Neurokinin Substance P Receptor Antagonist (−)-L-733,061 and (−)-Deoxocassine. J. Org. Chem. 2004, 69, 6001. <>
  • Omar Enouri A., Tu Chi, Wigal Carl T., Braun Loren L.: The meyer-schuster rearrangement and hydrohalide addition of 3-alkynyl-3-hydroxy-1H-isoindol-1-ones. Journal of Heterocyclic Chemistry 1992, 29, 947. <>
  • Flitsch Wilhelm: Zur Umsetzung cyclischer Imide mit Allylmagnesiumbromid. Justus Liebigs Ann. Chem. 1965, 684, 141. <>