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Reaction of Elemol with Acetic Acid/Perchloric Acid: Characterization of a Novel Oxide and (+)‐β‐Cyperone
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/hlca.19560390329openalex-snapshot
Zur Kenntnis der Sesquiterpene und Azulene. 116. Mitteilung. Über die absolute Konfiguration des α‐Santonins
inferredcites →https://doi.org/10.1016/0040-4020(94)00938-qopenalex-snapshot
Biotransformation of (±)-4,8-dimethylcyclodeca-3(E),7(E)- dien-1β-ol and (+)-hedycaryol by Cichorium intybus
inferredcites →https://doi.org/10.1016/0040-4020(96)00571-6openalex-snapshot
Ring-opening aminolysis of sesquiterpene lactones: An easy entry to bioactive sesquiterpene derivatives. Synthesis of (+)-β-cyperone and (−)-eudesma-3,5-diene from santonin
inferredcites →https://doi.org/10.1039/jr9360000667openalex-snapshot
152. α-Cyperone, a sesquiterpene ketone from the oil of Cyperus rotundus
inferredcites →https://doi.org/10.1039/jr9370001576openalex-snapshot
330. Synthetic cyperones and their comparison with α- and β-cyperones
inferredcites →https://doi.org/10.1039/jr9540003492openalex-snapshot
Sesquiterpenoids. Part IV. The constitution of carissone
inferredcites →https://doi.org/10.1039/jr9550002423openalex-snapshot
The structure of cyperone. Part IV. The synthesis of (natural)(+)-α-cyperone, its enantiomorph, and an epimer
inferredcites →https://doi.org/10.1039/jr9640001029openalex-snapshot
199. Studies in the synthesis of terpenes. Part VIII. The absolute configuration of elemol
inferredcites →https://doi.org/10.1080/00397917608072632openalex-snapshot
A New Synthesis and the13C-NMR OF β-Cyperone 1,3-Dibromo-2-Pentene, A New Ethyl Vinyl Ketone Equivalent
inferredcites →https://doi.org/10.1139/v80-422openalex-snapshot
The chemistry of thujone. III. Thujone as a chiral synthon for the preparation of sesquiterpenes. Synthesis of (+)-β-cyperone
What points at this work
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inferred← citeshttps://doi.org/10.2139/ssrn.4530288openalex-extracted
From Elemol to Fragranced Elemoxide: Synthesis, Bioactivity, and Molecular Docking Insights as Tyrosinase Inhibitor
inferred← citeshttps://doi.org/10.1016/j.seppur.2025.134107openalex-snapshot
Enhanced extraction of Schinus molle L. volatile compounds using sustainable solvents
inferred← citeshttps://doi.org/10.1016/j.tet.2009.04.062openalex-snapshot
(−)-trans-β-Elemene and related compounds: occurrence, synthesis, and anticancer activity
inferred← citeshttps://doi.org/10.1021/ol8029017openalex-snapshot
Synthesis of Enantiopure Bicyclic α,α-Disubstituted Spirolactams via Asymmetric Birch Reductive Alkylation
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