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Chemistry of Natural Compounds

, Volume 55, Issue 4, pp 705–708 | Cite as

Reduction of Norfluorocurarine and α-Methyleneindoline Alkaloids

  • Sh. M. Adizov
  • A. G. Eshimbetov
  • B. TashkhodzhaevEmail author
  • M. M. Mirzaeva
  • P. Kh. Yuldashev
Article
  • 5 Downloads

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.

Keywords

indole alkaloids norfluorocurarine reduction 

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  • Sh. M. Adizov
    • 1
  • A. G. Eshimbetov
    • 1
  • B. Tashkhodzhaev
    • 1
    Email author
  • M. M. Mirzaeva
    • 1
  • P. Kh. Yuldashev
    • 1
  1. 1.S. Yu. Yunusov Institute of the Chemistry of Plant SubstancesAcademy of Sciences of the Republic of UzbekistanTashkentUzbekistan

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