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Reduction of Norfluorocurarine and α-Methyleneindoline Alkaloids

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Chemistry of Natural Compounds Aims and scope

Reduction of the alkaloid norfluorocurarine, which may adopt a zwitterionic form in basic medium but reverts to the initial state in acidic and neutral media according to UV and IR spectroscopy and an X-ray structure analysis, was studied. Alkaloids of the α-methyleneindoline type formed indolenine species in acidic and neutral media; indole derivatives, in basic medium.

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Authors and Affiliations

  1. S. Yu. Yunusov Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan, Tashkent, Uzbekistan

    Sh. M. Adizov, A. G. Eshimbetov, B. Tashkhodzhaev, M. M. Mirzaeva & P. Kh. Yuldashev

Authors
  1. Sh. M. Adizov
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  2. A. G. Eshimbetov
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  3. B. Tashkhodzhaev
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  4. M. M. Mirzaeva
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  5. P. Kh. Yuldashev
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Corresponding author

Correspondence to B. Tashkhodzhaev.

Additional information

Translated from Khimiya Prirodnykh Soedinenii, No. 4, July–August, 2019, pp. 601–604.

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Adizov, S.M., Eshimbetov, A.G., Tashkhodzhaev, B. et al. Reduction of Norfluorocurarine and α-Methyleneindoline Alkaloids. Chem Nat Compd 55, 705–708 (2019). https://doi.org/10.1007/s10600-019-02783-8

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  • DOI: https://doi.org/10.1007/s10600-019-02783-8

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