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Evolution and Occurrence of 1,8-Cineole (Eucalyptol) in Australian Wine
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/hc.20044openalex-snapshot
A simple, convenient and expeditious approach to cineol
inferredcites →https://doi.org/10.1002/hlca.19960790606openalex-snapshot
Determination of the Configuration of Wine Lactone
inferredcites →https://doi.org/10.1002/mnfr.200900528openalex-snapshot
Quantification of 1,8‐cineole and of its metabolites in humans using stable isotope dilution assays
inferredcites →https://doi.org/10.1016/0021-9673(92)85063-yopenalex-snapshot
Eucalyptus leaf oils: use, chemistry, distillation and marketing
inferredcites →https://doi.org/10.1016/j.aca.2004.02.002openalex-snapshot
Comparative analysis of volatile compounds of ?fino? sherry wine by rotatory and continuous liquid?liquid extraction and solid-phase microextraction in conjunction with gas chromatography-mass spectrometry
inferredcites →https://doi.org/10.1016/j.fct.2003.11.001openalex-snapshot
1,8-cineole (eucalyptol), a monoterpene oxide attenuates the colonic damage in rats on acute TNBS-colitis
inferredcites →https://doi.org/10.1016/j.jep.2003.09.007openalex-snapshot
Analgesic and anti-inflammatory effects of essential oils of Eucalyptus
inferredcites →https://doi.org/10.1021/ja00531a020openalex-snapshot
Phenylselenoetherification. A highly efficient cyclization process for the synthesis of oxygen- and sulfur-heterocycles
inferredcites →https://doi.org/10.1021/jf030087iopenalex-snapshot
Aroma Composition ofVitis viniferaCv. Tannat: the Typical Red Wine from Uruguay
inferredcites →https://doi.org/10.1021/jf040332dopenalex-snapshot
Terpene Compounds as Possible Precursors of 1,8-Cineole in Red Grapes and Wines
inferredcites →https://doi.org/10.1021/jf960039gopenalex-snapshot
Influence of Ethanol on Pesticide Extraction in Aqueous Solutions by Solid-Phase Microextraction
inferredcites →https://doi.org/10.1021/jo01021a508openalex-snapshot
Diels—Alder Reactions of Acrylic Acid Derivatives Catalyzed by Aluminum Chloride
inferredcites →https://doi.org/10.1021/jo01304a046openalex-snapshot
A new route to simple monoterpenes by remote functionalization
inferredcites →https://doi.org/10.1021/ol060569qopenalex-snapshot
[AlCl3 + 2THF]: A New and Efficient Catalytic System for Diels−Alder Cycloaddition of α,β-Unsaturated Carbonyl Compounds under Solvent-Free Conditions
inferredcites →https://doi.org/10.1039/a802950dopenalex-snapshot
Proton chemical shifts in NMR. Part 12.1 Steric, electric field and conformational effects in acyclic and cyclic ethers
inferredcites →https://doi.org/10.1071/ch01168openalex-snapshot
9,10-Dihydroxy-1,8-cineole (1,3,3-Trimethyl-2-oxabicyclo[2.2.2]octane-10,11-diol)
inferredcites →https://doi.org/10.1111/j.1755-0238.2009.00065.xopenalex-snapshot
Identification and analysis of 2-chloro-6-methylphenol, 2,6-dichlorophenol and indole: causes of taints and off-flavours in wines
inferredcites →https://doi.org/10.1111/j.1755-0238.2010.00096.xopenalex-snapshot
Comparison of major volatile compounds from Riesling and Cabernet Sauvignon grapes (Vitis vinifera L.) from fruitset to harvest
inferredcites →https://doi.org/10.2105/ajph.2005.078014openalex-snapshot
Pharmacological and Chemical Effects of Cigarette Additives
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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A Two-Run Two-Dimensional Gas Chromatography Method Using Flame Ionization and Mass Spectrometry for the Automated and Robust Determination of the Nearly Complete Wine Aroma-Volatile Profile
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inferred← citeshttps://doi.org/10.1021/acs.jafc.6b03042openalex-snapshot
1,8-Cineole in French Red Wines: Evidence for a Contribution Related to Its Various Origins
inferred← citeshttps://doi.org/10.1021/acs.jafc.9b07165openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jf204499hopenalex-snapshot
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