Structures of ent-herbertane sesquiterpenoids displaying antifungal properties from the liverwort Herberta adunca
- 1 January 1986
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 4,p. 701-710
- https://doi.org/10.1039/p19860000701
Abstract
Several aromatic sesquiterpenoids displaying antifungal properties have been isolated from the liverwort Herberta adunca together with a mother hydrocarbon with a novel irregular sesquiterpene skeleton, ent-herbertane, and their structures and absolute configurations have been determined on the basis of extensive degradation reactions and spectroscopic evidence. The biological activity is also described.This publication has 6 references indexed in Scilit:
- Enantiomeric type sesquiterpenoids of the liverwort Marchantia polymorphaPhytochemistry, 1985
- Structure and absolute configuration of (+)-vitrenal, a novel carbon skeletal sesquiterpenoid having plant-growth-inhibitory activity, from the liverwort Lepidozia vitreaJournal of the Chemical Society, Perkin Transactions 1, 1984
- Structures and conformations of (–)-isobicyclogermacrenal and (–)-lepidozenal, two key sesquiterpenoids of the cis- and trans-10,3-bicyclic ring systems, from the liverwort Lepidozia vitrea : X-ray crystal structure analysis of the hydroxy derivative of (–)-isobicyclogermacrenalJournal of the Chemical Society, Perkin Transactions 1, 1984
- Structures of ent-2,3-secoalloaromadendrane sesquiterpenoids, which have plant-growth-inhibitory activity, from Plagiochila semidecurrens(liverwort)Journal of the Chemical Society, Perkin Transactions 1, 1981
- A spectrophotometric method for the detection of o-dihydroxyl groups in flavonoid compoundsArchives of Biochemistry and Biophysics, 1956
- The isoprene rule and the biogenesis of terpenic compoundsCellular and Molecular Life Sciences, 1953