Modification of Azepanobetulin at the Isopropenyl Group

Modification of the isopropenyl group of biologically active azepanobetulin via oxidation with ozone and selenium dioxide, allylic bromination, azidation, amination, reduction, 1,3-dipolar cycloaddition, and Claisen–Schmidt condensation afforded a series of C 30 -derivatives with oxygen- and nitroge...

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Veröffentlicht in:Russian journal of organic chemistry 2020-09, Vol.56 (9), p.1582-1587
Hauptverfasser: Petrova, A. V., Lopatina, T. V., Mustafin, A. G., Kazakova, O. B.
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Sprache:eng
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Zusammenfassung:Modification of the isopropenyl group of biologically active azepanobetulin via oxidation with ozone and selenium dioxide, allylic bromination, azidation, amination, reduction, 1,3-dipolar cycloaddition, and Claisen–Schmidt condensation afforded a series of C 30 -derivatives with oxygen- and nitrogen-containing aliphatic and heterocyclic substituents.
ISSN:1070-4280
1608-3393
DOI:10.1134/S1070428020090134