A REACTION OF BERBERINE WITH AMIDES IN ALKALINE MEDIA: AN EXPERIMENTAL AND QUANTUM CHEMICAL STUDY
DOI:
https://doi.org/10.1007/6681Keywords:
berberine, dihydroberberine, nucleophilic substitution, N-nucleophiles, DFT calculations.Abstract
The possibility of obtaining electroneutral 8-amido derivatives of dihydroberberines was shown experimentally and with the support of quantum chemical calculations based on the density functional theory (B3LYP/6-311+G(d,p)). In alkaline media, amides deprotonated to form amide anions, which, in turn, could add to the berberine framework at the C-8 position. Competing processes in this case were the reactions of the formation of 8-hydroxy- or 8-alkoxyberberines.
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Published
2022-07-21
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Short Communications