Incorporation of the enantiomeric [1-2H]cadaverines into the quinolizidine alkaloid (–)- anagyrine in Anagyris foetida
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1991/P1/P19910002353
Reference15 articles.
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2. Incorporation of [1,2-13C2]cadaverine and the enantiomeric [1-2H]cadaverines into the quinolizidine alkaloids in Baptisia australis
3. Deuteron NMR spectroscopy as a probe of the stereochemistry of biosynthetic reactions: the biosynthesis of lupanine and sparteine
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1. ChemInform Abstract: Incorporation of the Enantiomeric (1-2H)Cadaverines into the Quinolizidine Alkaloid (-)-Anagyrine in Anagyris foetida.;ChemInform;2010-08-22
2. Total Synthesis of (±)-α-Isosparteine, (±)-β-Isosparteine, and (±)-Sparteine from a Common Tetraoxobispidine Intermediate;The Journal of Organic Chemistry;2008-09-18
3. Biosynthesis and Metabolic Pathways: Deuterium NMR;Encyclopedia of Magnetic Resonance;2007-03-15
4. Thermopsideae (Abb. 130);Chemotaxonomie der Pflanzen;2001
5. Oxidative Deamination of Tetrahydroanabasine with o-Quinones: An Easy Entry to Lupinine, Sparteine, and Anabasine;The Journal of Organic Chemistry;1996-01-01
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