## Abstract The phytochemical investigation of extracts from the branch wood and branch barks of __Andira surinamensis__ yielded a novel isoflavone dimer, 4′‐methoxyisoflavone‐(7‐O‐7″)‐3″′,4″′‐methylenedioxyisoflavone (surinamensin), along with the triterpene lupeol and the known isoflavones 5,7‐di
NMR spectral assignments of a new chlorotryptamine alkaloid and its analogues from Acacia confusa
✍ Scribed by Malcolm S. Buchanan; Anthony R. Carroll; David Pass; Ronald J. Quinn
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 99 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1959
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✦ Synopsis
Abstract
A new chlorotryptamine alkaloid, N‐chloromethyl‐N,N‐dimethyltryptamine, was isolated from a methanol extract of the Chinese shrub Acacia confusa Merr., together with its known hallucinogenic analogues, N‐methyltryptamine, N,N‐dimethyltryptamine and N,N‐dimethyltryptamine‐N‐oxide. The new compound was an artefact of the isolation conditions. The complete ^1^H and ^13^C NMR assignments for these compounds were carried out using ^1^H, ^13^C, DEPT, gCOSY, gHSQC and gHMBC NMR experiments. Copyright © 2007 John Wiley & Sons, Ltd.
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