Phototransformation products of the alkaloid lappaconitine: Multinuclear NMR study Full article
Journal |
Journal of Photochemistry and Photobiology A: Chemistry
ISSN: 1010-6030 |
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Output data | Year: 2008, Volume: 197, Number: 2-3, Pages: 290-294 Pages count : DOI: 10.1016/j.jphotochem.2008.01.006 | ||||||
Tags | lappaconitine; phototransformation; N-acetylanthranilic acid; NMR | ||||||
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Abstract:
The NMR technique has been applied to characterize the phototransformation products of the natural alkaloid lappaconitine. It was demonstrated that the photolysis of lappaconitine 1 results in cleavage of the ester bond with elimination of N-acetylanthranilic acid. The final reaction product was found to be an immonium salt 4 of N-acetylanthranilic acid and enamine 3. An equilibrium between the imine cation and the enamine 3 was detected. (c) 2008 Elsevier B.V. All rights reserved.
Cite:
Polyakov N.E.
, Leshina T.V.
, Tkachev A.V.
, Nikitina I.A.
, Pankrushina N.A.
Phototransformation products of the alkaloid lappaconitine: Multinuclear NMR study
Journal of Photochemistry and Photobiology A: Chemistry. 2008. V.197. N2-3. P.290-294. DOI: 10.1016/j.jphotochem.2008.01.006 WOS Scopus РИНЦ
Phototransformation products of the alkaloid lappaconitine: Multinuclear NMR study
Journal of Photochemistry and Photobiology A: Chemistry. 2008. V.197. N2-3. P.290-294. DOI: 10.1016/j.jphotochem.2008.01.006 WOS Scopus РИНЦ
Dates:
Published print: | Jun 1, 2008 |
Identifiers:
Web of science | WOS:000256780100022 |
Scopus | 2-s2.0-43049134858 |
Elibrary | 22149105 |
OpenAlex | W1977376483 |