A diarylheptanoid intermediate in the biosynthesis of phenylphenalenones in Anigozanthos preissii
- 1 January 1995
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 5,p. 525-526
- https://doi.org/10.1039/c39950000525
Abstract
The incorporation of 1-phenyl-7-(3,4-dihydroxyphenyl)hepta-1,3-dien-5-one and two molecules of cinnamic acid, respectively, into anigorufone by cultured roots of Anigozanthos preissii provides the first experimental evidence for the biosynthesis of a phenylphenalenone from two C6–C3 units via an open chain type diarylheptanoid.Keywords
This publication has 17 references indexed in Scilit:
- Phenalenone-type phytoalexins from Musa acuminata synthesis of 4-phenyl-phenalenonesTetrahedron, 1994
- Two Novel Phenalenones from Dilatris viscosaJournal of Natural Products, 1993
- Irenolone and emenolone: two new types of phytoalexin from Musa paradisiacaThe Journal of Organic Chemistry, 1993
- Dimeric phenalene metabolites from Eichhornia crassipesTetrahedron, 1992
- Phenalene metabolites from eichhornia crassipesBioorganic & Medicinal Chemistry Letters, 1992
- Phylogeny and Classification of the HaemodoraceaeAnnals of the Missouri Botanical Garden, 1990
- The biosynthesis of 2,5,6-trihydroxy-9-phenylphenalenone by Lachnanthes tinctoria. Incorporation of 1-13C-phenylalanineTetrahedron Letters, 1977
- Colouring Matters of Australian Plants. XVIII. Constituents of Anigozanthos rufusAustralian Journal of Chemistry, 1975
- Biosynthesis of a 9-phenylperinaphthenone by Lachnanthes tinctoriaPhytochemistry, 1972
- The biosynthesis of the plant phenalenone haemocorinJournal of the Chemical Society D: Chemical Communications, 1971