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Collect. Czech. Chem. Commun. 1969, 34, 2809-2818
https://doi.org/10.1135/cccc19692809

Alkaloids from Vinca minor L. XXIII. Mass spectrometry of eburnamine-type alkaloids

V. Kováčik and I. Kompiš

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  • Vrabec Rudolf, Maříková Jana, Ločárek Miroslav, Korábečný Jan, Hulcová Daniela, Hošťálková Anna, Kuneš Jiří, Chlebek Jakub, Kučera Tomáš, Hrabinová Martina, Jun Daniel, Soukup Ondřej, Andrisano Vincenza, Jenčo Jaroslav, Šafratová Marcela, Nováková Lucie, Opletal Lubomír, Cahlíková Lucie: Monoterpene indole alkaloids from Vinca minor L. (Apocynaceae): Identification of new structural scaffold for treatment of Alzheimer's disease. Phytochemistry 2022, 194, 113017. <https://doi.org/10.1016/j.phytochem.2021.113017>
  • Abouzeid Sara, Beutling Ulrike, Selmar Dirk: Stress-induced modification of indole alkaloids:Phytomodificines as a new category of specialized metabolites. Phytochemistry 2019, 159, 102. <https://doi.org/10.1016/j.phytochem.2018.12.015>
  • Abouzeid Sara, Beutling Ulrike, Surup Frank, Abdel Bar Fatma M., Amer Mohamed M., Badria Farid A., Yahyazadeh Mahdi, Brönstrup Mark, Selmar Dirk: Treatment of Vinca minor Leaves with Methyl Jasmonate Extensively Alters the Pattern and Composition of Indole Alkaloids. J. Nat. Prod. 2017, 80, 2905. <https://doi.org/10.1021/acs.jnatprod.7b00424>
  • Akhgari Amir, Laakso Into, Seppänen-Laakso Tuulikki, Yrjönen Teijo, Vuorela Heikki, Oksman-Caldentey Kirsi-Marja, Rischer Heiko: Analysis of Indole Alkaloids from Rhazya stricta Hairy Roots by Ultra-Performance Liquid Chromatography-Mass Spectrometry. Molecules 2015, 20, 22621. <https://doi.org/10.3390/molecules201219873>
  • Bauerle Gerald F., Hall Brad J., Tran Ngoc V., Brodbelt Jennifer S.: Ion-molecule reactions of oxygenated chemical ionization reagents with vincamine. J. Am. Soc. Mass Spectrom. 1996, 7, 250. <https://doi.org/10.1016/1044-0305(95)00650-8>
  • Czira Gábor, Tamás József, Kalaus György: Effects of stereoisomerism on the electron impact fragmentation of some compounds with an eburnane skeleton1. Org. Mass Spectrom. 1984, 19, 555. <https://doi.org/10.1002/oms.1210191106>
  • Bombardelli E., Bonati A., Gabetta B., Martinelli E.M., Mustich G., Danieli B.: The structure of cuanzine. Tetrahedron 1974, 30, 4141. <https://doi.org/10.1016/S0040-4020(01)97398-3>
  • Burlingame A L., Johanson G A.: Mass Spectrometry. Anal. Chem. 1972, 44, 337. <https://doi.org/10.1021/ac60313a601>
  • Sutherland Jerry W., Williamson David E., Theivagt James G.: Pharmaceuticals and related drugs. Anal. Chem. 1971, 43, 206. <https://doi.org/10.1021/ac60300a027>
  • DeJongh Don C.: Mass spectrometry. Anal. Chem. 1970, 42, 169. <https://doi.org/10.1021/ac60287a002>