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Updated: Aug 8, 2026

Syntheses, Crystallization, and Spectroscopic Characterization of 3,5-Lutidine N-Oxide Dehydrate
Published on: April 24, 2018
Epoxidation in vivo of hyoscyamine to scopolamine does not involve a dehydration step
T Hashimoto1, J Kohno, Y Yamada
1Research Center for Cell and Tissue Culture, Faculty of Agriculture, Kyoto University, Kyoto 606, Japan.
Abstract:
Hyoscyamine is epoxidized to scopolamine via 6beta-hydroxyhyoscyamine in several solanaceous plants. 6,7-Dehydrohyoscyamine has been proposed to be an intermediate in the conversion of 6beta-hydroxyhyoscyamine to scopolamine on the basis of the observation that this unsaturated alkaloid is converted to scopolamine when fed to a Datura scion. To determine whether a dehydration step is involved in scopolamine biosynthesis, [6-(18)O]6beta-hydroxyhyoscyamine was prepared from l-hyoscyamine and (18)O(2) using hyoscyamine 6beta-hydroxylase obtained from root cultures of Hyoscyamus niger L. When [6-(18)O]6beta-hydroxyhyoscyamine was fed to shoot cultures of Duboisia myoporoides R. B(R)., the labeled alkaloid was converted to scopolamine which retained (18)O in the epoxide oxygen. It is concluded that 6beta-hydroxyhyoscyamine is converted in vivo to scopolamine without a dehydration step.
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