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Relationship of Anthricin, Hernandion and Cicutin to Desoxypodophyllotoxin

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Download Hi-Res ImageDownload to MS-PowerPointCite This:J. Am. Chem. Soc. 1954, 76, 15, 4034-4035
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    Relationship of Anthricin, Hernandion and Cicutin to Desoxypodophyllotoxin
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    Journal of the American Chemical Society

    Cite this: J. Am. Chem. Soc. 1954, 76, 15, 4034–4035
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    https://doi.org/10.1021/ja01644a056
    Published August 1, 1954
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    Cited By

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    This article is cited by 18 publications.

    1. George R. Pettit, Fiona Hogan, Jun-Ping Xu, Rui Tan, Toshihiko Nogawa, Zbigniew Cichacz, Robin K. Pettit, Jiang Du, Qing-Hua Ye, Gordon M. Cragg, Cherry L. Herald, Michael S. Hoard, Animesh Goswami, Justin Searcy, Larry Tackett, Dennis L. Doubek, Lee Williams, John N. A. Hooper, Jean M. Schmidt, Jean-Charles Chapuis, Denise N. Tackett and Felicia Craciunescu. Antineoplastic Agents. 536. New Sources of Naturally Occurring Cancer Cell Growth Inhibitors from Marine Organisms, Terrestrial Plants, and Microorganisms,. Journal of Natural Products 2008, 71 (3) , 438-444. https://doi.org/10.1021/np700738k
    2. Caitlyn D. Carpenter, Taryn O'Neill, Nadia Picot, John A. Johnson, Gilles A. Robichaud, Duncan Webster, Christopher A. Gray. Anti-mycobacterial natural products from the Canadian medicinal plant Juniperus communis. Journal of Ethnopharmacology 2012, 143 (2) , 695-700. https://doi.org/10.1016/j.jep.2012.07.035
    3. Shi-long Wang, Si-de Yao, Wang Mei, Yu-long Zhang, Man-wei Zhang, Zhi-cheng Zhang. The mechanism of photo-ionization of podophyllotoxin and its derivatives:. Radiation Physics and Chemistry 1998, 53 (6) , 623-628. https://doi.org/10.1016/S0969-806X(97)00286-7
    4. Jih-Jung Chen, Ian-Lih Tsai, Tsutomu Ishikawa, Chyl-Jia Wang, Ih-Sheng Chen. Alkaloids from trunk bark of Hernandia nymphaeifolia. Phytochemistry 1996, 42 (5) , 1479-1484. https://doi.org/10.1016/0031-9422(96)00123-9
    5. Ih-Sheng Chen, Jih-Jung Chen, Ian-Lih Tsai. Alkaloids from Hernandia sonora. Phytochemistry 1995, 40 (3) , 983-986. https://doi.org/10.1016/0031-9422(95)00280-K
    6. Masao Arimoto, H. Yamaguchi, S. Nishibe. Structure Elucidation and Synthesis of the Lignans from the Seeds of Hernandia ovigera L.. 1995, 551-606. https://doi.org/10.1016/S1572-5995(96)80034-2
    7. Toshiaki Morimoto, Mitsuo Chiba, Kazuo Achiwa. Efficient asymmetric syntheses of naturally occurring lignan lactones using catalytic asymmetric hydrogenation as a key reaction. Tetrahedron 1993, 49 (9) , 1793-1806. https://doi.org/10.1016/S0040-4020(01)80536-6
    8. Toshiaki Morimoto, Mitsuo Chiba, Kazuo Achiwa. Asymmetric total synthesis of (−)-deoxypodophyllotoxin. Tetrahedron Letters 1990, 31 (2) , 261-264. https://doi.org/10.1016/S0040-4039(00)94387-9
    9. Walter Karrer. Lignane. 1976, 461-476. https://doi.org/10.1007/978-3-0348-5142-8_12
    10. Graeme B. Russell. Lignans and sugiol from Libocedrus bidwillii. Phytochemistry 1975, 14 (12) , 2708. https://doi.org/10.1016/0031-9422(75)85256-3
    11. R. Hegnauer. Umbelliferae. 1973, 554-629. https://doi.org/10.1007/978-3-0348-9379-4_52
    12. M. Kuhn, A. Von Wartbung. Podophyllum ‐ Lignane: Struktur und Absolutkonfiguration von Podorhizol‐β‐ D ‐glucosid ( = Lignan F). 19. Mitt. über mitosehemmende Naturstoffe [1]. Helvetica Chimica Acta 1967, 50 (6) , 1546-1565. https://doi.org/10.1002/hlca.19670500614
    13. TADEUSZ KORZYBSKI, ZUZANNA KOWSZYK-GINDIFER, WŁODZIMIERZ KURYŁOWICZ. PODOPHYLLOTOXIN. 1967, 1502-1504. https://doi.org/10.1016/B978-1-4831-9801-9.50246-4
    14. Jany Renz, Max Kuhn, Albert Von Wartburg. Synthese des Neopodophyllotoxins und der Podophyllinsäure Umesterungsreaktionen an Podophyllum‐Lignanen. Justus Liebigs Annalen der Chemie 1965, 681 (1) , 207-224. https://doi.org/10.1002/jlac.19656810129
    15. Max Kuhn, A. von Wartburg. Desoxypodophyllinsäure‐1 β‐D‐glucopyranosyl‐ester, ein neues. Lignanderivat aus Podophyllum peltatum L. und P. emodi W ALL . 13. Mitteilung über mitosehemmende Naturstoffe. Helvetica Chimica Acta 1963, 46 (6) , 2127-2139. https://doi.org/10.1002/hlca.19630460632
    16. N. Narasimhachari, E. von Rudloff. THE CHEMICAL COMPOSITION OF THE WOOD AND BARK EXTRACTIVES OF JUNIPERUS HORIZONTALIS MOENCH. Canadian Journal of Chemistry 1961, 39 (12) , 2572-2581. https://doi.org/10.1139/v61-339
    17. Walter Karrer. Lignane. 1958, 461-476. https://doi.org/10.1007/978-3-0348-6808-2_12
    18. J. L. Hartwell, A. W. Schrecker. The Chemistry of Podophyllum. 1958, 83-166. https://doi.org/10.1007/978-3-7091-7162-2_3
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    Journal of the American Chemical Society

    Cite this: J. Am. Chem. Soc. 1954, 76, 15, 4034–4035
    Click to copy citationCitation copied!
    https://doi.org/10.1021/ja01644a056
    Published August 1, 1954
    Request reuse permissions

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