Author:
Křen Vladimír,Němeček Jan,Přikrylová Věra
Abstract
Both possible 6-N-oxides of agroclavine (I) and elymoclavine (II) were prepared by hydrogen peroxide oxidation. Their 1H and 13C NMR spectra were assigned and the conformation of the D ring (half-chair) was determined. Absolute configuration at 6-N was established by NMR and molecular modelling.
Publisher
Institute of Organic Chemistry & Biochemistry
Cited by
5 articles.
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