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Terpenoids Derived from Linalyl Oxide. Part 1. The stereochemistry of the davanones
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/hlca.19630460507openalex-snapshot
Zur Kenntnis ätherischer Öle. 2. Mitteilung. Die Struktur der sogenannten «Linalooloxide»
inferredcites →https://doi.org/10.1002/hlca.19640470227openalex-snapshot
Zur Darstellung von Tetrahydropyran‐ und Tetrahydrofuran‐derivaten aus 1,7‐ bzw. 1,6‐Allyldiolen durch Dehydratation in der Allylstellung
inferredcites →https://doi.org/10.1002/hlca.19700530422openalex-snapshot
Zur Stereochemie des (+)‐Davanons
inferredcites →https://doi.org/10.1002/recl.19680870613openalex-snapshot
The structure of davanone a new sesquiterpene from davana: (Artemisia pallens, Wall.)
inferredcites →https://doi.org/10.1016/0006-291x(73)91259-xopenalex-snapshot
Carbon-13 nuclear magnetic resonance spectral analysis of C-nucleosides. The structure of pyrazomycin B1
inferredcites →https://doi.org/10.1016/s0040-4020(01)98341-3openalex-snapshot
Solvent effects in NMR spectroscopy—III
inferredcites →https://doi.org/10.1016/s0040-4039(01)97878-5openalex-snapshot
The total synthesis of racemic davanone
inferredcites →https://doi.org/10.1021/ja00735a049openalex-snapshot
New superior paramagnetic shift reagents for nuclear magnetic resonance spectral clarification
inferredcites →https://doi.org/10.1021/ja00979a048openalex-snapshot
Torsional Effects in Polycyclic Systems. II. The Stereochemistry of Attack and Departure in Norbornane Derivatives
inferredcites →https://doi.org/10.1021/ja00991a040openalex-snapshot
Protonic acid additions to 1-methylnorbornene. Absence of orientational control attributable to participation
inferredcites →https://doi.org/10.1071/ch9701811openalex-snapshot
A non-stereospecific synthesis of (±)-davanone
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113548zenodo-depositor-declared
Arteperoxides A–C, tris-normonoterpene–sesquiterpene conjugates with peroxide-bridges from Artemisia judaica exhibiting antiosteoclastogenic activity
inferred← citeshttps://doi.org/10.1002/ardp.19793120511openalex-snapshot
Neue Substanzen aus ätherischen Ölen verschiedener Artemisia‐Species, 2. Mitt. Davanon, ein furanoides Sesquiterpenketon
inferred← citeshttps://doi.org/10.1002/ardp.19793121107openalex-snapshot
Neue Substanzen aus ätherischen Ölen verschiedener Artemisia‐Species, 4. Mitt. Hydroxy‐Davanon, ein furanoider Sesquiterpenalkohol
inferred← citeshttps://doi.org/10.1002/ardp.19933260806openalex-snapshot
Peroxide als Pflanzeninhaltsstoffe, 12. Mitt.: Peroxide vom Davanon‐Typ aus der Eberraute (Artemisia abrotanum) und ihre Darstellung
inferred← citeshttps://doi.org/10.1002/cbdv.202100531openalex-snapshot
New Insights into the Chemical Composition, Pro‐Inflammatory Cytokine Inhibition Profile of Davana (Artemisia pallens Wall. ex DC.) Essential Oil and cis‐Davanone in Primary Macrophage Cells
inferred← citeshttps://doi.org/10.1002/chin.197504064openalex-snapshot
ChemInform Abstract: TERPENOIDS DERIVED FROM LINALYL OXIDE PART 1, THE STEREOCHEMISTRY OF THE DAVANONES
inferred← citeshttps://doi.org/10.1002/hlca.19740570718openalex-snapshot
Terpenoids Derived from Linalyl Oxide. Part 3. The isolation, structure, absolute configuration and synthesis of the davanafurans, nor‐sesquiterpenes isolated from Artemisia Pallens
inferred← citeshttps://doi.org/10.1002/hlca.19740570719openalex-snapshot
Terpenoids Derived from Linalyl Oxide, Part 4. The oxidation of davanone. Isolation and synthesis of the davana ethers, sesquiterpenes of Artemisia Pallens
inferred← citeshttps://doi.org/10.1002/hlca.19740570720openalex-snapshot
Terpenoids Derived from Linalyl Oxide. Part 5. 2‐(2‐Methyl‐2‐vinyltetrahydrofur‐5‐yl)‐2,6,6‐trimethyl‐2,6‐dihydropyr‐3‐one, a new sesquiterpenoid isolated from Artemisia Pallens
inferred← citeshttps://doi.org/10.1002/hlca.19790620618openalex-snapshot
Inhaltsstoffe des Osmanthus‐Absolues 6. Mitteilung. (7S, 10S, 5E)‐ und (7R, 10S, 5E)‐2,6,10‐Trimethyl‐7,10‐epoxy‐2,5,11‐dodecatrien
inferred← citeshttps://doi.org/10.1002/hlca.19800630130openalex-snapshot
Synthesis and Configuration of the Eight Diastereoisomeric Racemates of Dactyloxene‐B. The relative configuration of dactyloxene‐B and ‐C
inferred← citeshttps://doi.org/10.1002/hlca.19920750502openalex-snapshot
75 Jahre Riechstoff‐ und Aroma‐Chemie im Spiegel der Helvetica Chimica Acta. Teil I
inferred← citeshttps://doi.org/10.1002/hlca.19920750702openalex-snapshot
75 Jahre Riechstoff‐und Aroma‐Chemie im Spiegel der Helvetica Chimica Acta.Teil II
inferred← citeshttps://doi.org/10.1002/jlac.198819880919openalex-snapshot
Terpenes and terpene derivatives, XXIV. Isolation and stereochemistry of the four artedouglasia oxides
inferred← citeshttps://doi.org/10.1002/mrc.1270170105openalex-snapshot
13C NMR spectral studies of zoapatanol and montanol, novel diterpenes from Montanoa tomentosa (zoapatle), and their chemical derivatives
inferred← citeshttps://doi.org/10.1007/978-3-7091-3265-4_1openalex-snapshot
The Use of Carbon-13 Nuclear Magnetic Resonance Spectroscopy in Natural Products Chemistry
inferred← citeshttps://doi.org/10.1007/s12272-011-0801-0openalex-snapshot
Studies on the chemical composition and possible mechanisms underlying the antispasmodic and bronchodilatory activities of the essential oil of Artemisia maritima L.
inferred← citeshttps://doi.org/10.1016/0020-1790(90)90041-ropenalex-snapshot
GC-MS and 13C-NMR studies on the biosynthesis of terpenoid defensive secretions by the larvae of papilionid butterflies (Luehdorfia and Papilio)
inferred← citeshttps://doi.org/10.1016/0031-9422(81)84018-6openalex-snapshot
Essential oils of five Tanacetum vulgare genotypes
inferred← citeshttps://doi.org/10.1016/0031-9422(90)85220-aopenalex-snapshot
Sesquiterpene ketones related to davanone from Artemisia pallens
inferred← citeshttps://doi.org/10.1016/0031-9422(91)83725-zopenalex-snapshot
Fragrant components of oil from Artemisia pallens
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00772-5openalex-snapshot
A germacranolide from Artemisia pallens
inferred← citeshttps://doi.org/10.1016/0040-4039(92)80010-hopenalex-snapshot
Directed oxidative cyclization of 5-hydroxyalkenes with rhenium oxide
inferred← citeshttps://doi.org/10.1016/0079-6565(82)80003-4openalex-snapshot
Computer assisted analysis of carbon-13 NMR spectral data
inferred← citeshttps://doi.org/10.1016/j.cclet.2009.03.041openalex-snapshot
Three new sesquiterpenes from Euonymus schensianus Maxim
inferred← citeshttps://doi.org/10.1016/j.fitote.2011.09.012openalex-snapshot
Sesquiterpenoids and norterpenoids from Vitex negundo
inferred← citeshttps://doi.org/10.1016/j.phytochem.2015.11.004openalex-snapshot
Intraspecific variation in essential oil composition of the medicinal plant Lippia integrifolia (Verbenaceae). Evidence for five chemotypes
inferred← citeshttps://doi.org/10.1016/j.tet.2005.01.131openalex-snapshot
Studies on t-BuOK-catalyzed Michael addition of 1,2-allenic ketones with 2-substituted diethyl malonates: highly selective synthesis of β,γ-unsaturated enones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.11.122openalex-snapshot
Palladium catalyzed reductive decarboxylation of allyl α-alkenyl-β-ketoesters. A new synthesis of (E)-3-alkenones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.08.109openalex-snapshot
t-BuOK promoted coupling of alkynes and aldehydes: a concise synthetic method of β,γ-unsaturated enones
inferred← citeshttps://doi.org/10.1016/s0031-9422(00)84096-0openalex-snapshot
Tetrahydrofuran-type terpenoids from Tanacetum vulgare
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)81657-3openalex-snapshot
A highly stereoselective synthesis of davanone
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)99933-7openalex-snapshot
Preparation d'oxydes de linalol par bioconversion
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)85855-xopenalex-snapshot
Mammalian pheromone studies - III. (e,e)-7,11,15-Trimethyl-3-methylenehexa- deca-1,6,10,14-tetraene, a new diterpene analogue of β-farnesene from the dorsal gland of the springbok, Antidorcas marsupialis
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)91378-4openalex-snapshot
Dihydrofurano-terpenoids of davana oil
inferred← citeshttps://doi.org/10.1016/s0305-1978(02)00082-0openalex-snapshot
Variations in the essential oil composition of Artemisia pedemontana gathered in Spain: chemotype camphor-1,8-cineole and chemotype davanone
inferred← citeshttps://doi.org/10.1021/ja1108694openalex-snapshot
A Straightforward Synthesis of Cyclobutenones via a Tandem Michael Addition/Cyclization Reaction of 2,3-Allenoates with Organozincs
inferred← citeshttps://doi.org/10.1021/jf062652yopenalex-snapshot
Isomeric Enhancement of Davanone from Natural Davana Oil Aided by Supercritical Carbon Dioxide
inferred← citeshttps://doi.org/10.1021/jo034633iopenalex-snapshot
Studies on K2CO3-Catalyzed 1,4-Addition of 1,2-Allenic Ketones with Diethyl Malonate: Controlled Selective Synthesis of β,γ-Unsaturated Enones and α-Pyrones
inferred← citeshttps://doi.org/10.1080/07391102.2020.1851301openalex-snapshot
Statistical analysis/theoretical investigations of novel vascular endothelial growth factor of Davanoide from Scolymus grandifloras Desf as potent anti-angiogenic drug properties
inferred← citeshttps://doi.org/10.1080/10412905.2011.9700449openalex-snapshot
Chemotypic Variation in IndianLantana camaraEssential Oil
inferred← citeshttps://doi.org/10.1080/10412905.2013.827478openalex-snapshot
Essential oils from Bolivia. XII. Asteraceae:Ophryosporus piquerioides(D.C.) Benth. ex Baker
inferred← citeshttps://doi.org/10.1177/1934578x1501000802openalex-snapshot
Arthropod Deterrents from Artemisia Pallens (Davana Oil) Components
inferred← citeshttps://doi.org/10.1246/cl.1987.1259openalex-snapshot
Stereoselective Syntheses of (+)-Davanone and (+)-Artemone via Anti-selective Epoxidation and Iodo-cyclization
inferred← citeshttps://doi.org/10.34172/jhp.2024.51511openalex-snapshot
Artemisia pallens Wall. ex. DC: A comprehensive review
inferred← citeshttps://doi.org/10.70675/f8fab165zef07z4589z8723z6d8e1eafdcedopenalex-snapshot
Extraction and characterization of the constituents contained in the extracts of Scolymus grandiflorus, Carduncellus pinnatus and Salvia argentea : evaluation of their biological activities
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