Incorporation of the enantiomeric [1-2H]cadaverines into the quinolizidine alkaloid (–)-anagyrine in Anagyris foetida

Brown, A. M., Rycroft, D. S. and Robins, D. J. (1991) Incorporation of the enantiomeric [1-2H]cadaverines into the quinolizidine alkaloid (–)-anagyrine in Anagyris foetida. Journal of the Chemical Society: Perkin Transactions 1, 10, pp. 2353-2355. (doi: 10.1039/P19910002353)

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Abstract

The labelling patterns in (–)-anagyrine 13 derived biosynthetically from (R)- and (S)-[1-2H]cadaverine 5 and 6, respectively, in Anagyris foetida have been established by 2H NMR spectroscopy. Comparison of the composite labelling pattern 14 with that 11 published for (+)-sparteine has distinguished between two possible pathways for conversion of a tetracyclic intermediate into (–)-anagyrine.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Rycroft, Dr David and Robins, Prof David
Authors: Brown, A. M., Rycroft, D. S., and Robins, D. J.
Subjects:Q Science > QD Chemistry
College/School:College of Science and Engineering > School of Chemistry
Journal Name:Journal of the Chemical Society: Perkin Transactions 1
Journal Abbr.:J. Chem. Soc., Perkin Trans. 1
Publisher:Royal Society of Chemistry
ISSN:0300-922X
ISSN (Online):2050-8255

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