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Collect. Czech. Chem. Commun. 1977, 42, 548-552

Vinoxine, a novel type of indole alkaloid

Z. Votický, E. Grossmann and P. Potier

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  • Okada Kosuke, Ueda Hirofumi, Tokuyama Hidetoshi: Total synthesis of (±)-vinoxine: construction of the bridged pyrido[1,2-a]indole skeleton via Tf2O-mediated Bischler–Napieralski reaction and stereoselective radical cyclization. Org. Biomol. Chem. 2022, 20, 5943. <>
  • Mauger Audrey, Jarret Maxime, Kouklovsky Cyrille, Poupon Erwan, Evanno Laurent, Vincent Guillaume: The chemistry of mavacurane alkaloids: a rich source of bis-indole alkaloids. Nat. Prod. Rep. 2021, 38, 1852. <>
  • Lood Christopher S., Laine Aino E., Högnäsbacka Antonia, Nieger Martin, Koskinen Ari M. P.: Synthesis of Chiral (Indol-2-yl)methanamines and Insight into the Stereochemistry Protecting Effects of the 9-Phenyl-9-fluorenyl Protecting Group. Eur. J. Org. Chem. 2015, 2015, 3793. <>
  • Bahadori Fatemeh, Topçu Gülaçtι, Boǧa Mehmet, Türkekul Ayla, Kolak Ufuk, Kartal Murat: Indole Alkaloids from Vinca major and V. minor Growing in Turkey. Natural Product Communications 2012, 7, 1934578X1200700. <>
  • Bennasar M.-Lluı̈sa, Zulaica Ester, Alonso Yolanda, Vidal Bernat, Vázquez Jesús T., Bosch Joan: Addition of chiral enolates to N-alkyl-3-acylpyridinium salts. Total synthesis of (+)-16-epivinoxine and (−)-vinoxine. Tetrahedron: Asymmetry 2002, 13, 95. <>
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  • Verpoorte R., van Beek T. A., Riegman R. L. M., Hylands P. J., Bisset N. G.: Aromatic chemical shifts inar-hydroxy- and -methoxy-substituted indole alkaloids; reference data and substituent-induced chemical shifts for ten different chromophoric groups. Org. Magn. Reson. 1984, 22, 328. <>
  • Bosch Joan, Bennasar M.-Lluïsa, Zulaica Ester, Feliz Miguel: Total synthesis and stereochemical reassignment of the indole alkaloid vinoxine. Tetrahedron Letters 1984, 25, 3119. <>
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  • VOTICKY Z., GROSSMANN E., POTIER P.: ChemInform Abstract: ALKALOIDS FROM VINCA MINOR L. XXV. VINOXINE, A NOVEL TYPE OF INDOLE ALKALOID. Chemischer Informationsdienst 1977, 8, no. <>