Reduction of Norfluorocurarine and [alpha]-Methyleneindoline Alkaloids

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 [alpha]-methyleneindoline type formed indol...

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Bibliographic Details
Published in:Chemistry of natural compounds 2019-07, Vol.55 (4), p.705
Main Authors: Adizov, Sh. M, Eshimbetov, A. G, Tashkhodzhaev, B, Mirzaeva, M. M, Yuldashev, P. Kh
Format: Article
Language:English
Subjects:
Alkaloids
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Summary: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 [alpha]-methyleneindoline type formed indolenine species in acidic and neutral media; indole derivatives, in basic medium.
ISSN:0009-3130
1573-8388
DOI:10.1007/s10600-019-02783-8