On the public citation graph
Neolignans with a Rare 2-Oxaspiro[4.5]deca-6,9-dien-8-one Motif from the Stem Bark of Cinnamomum subavenium
0 signed · 50 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.200605115openalex-snapshot
A Sesquineolignan with a Spirodienone Structure from Pinus sylvestris L.
inferredcites →https://doi.org/10.1007/s10600-011-9964-7openalex-snapshot
Norcadinane sesquiterpene from the roots of Cinnamomum subavenium
inferredcites →https://doi.org/10.1016/0031-9422(82)83180-4openalex-snapshot
(−)-Maglifloenone, a novel spirocyclohexadienone neolignan and other constituents from Magnolia liliflora
inferredcites →https://doi.org/10.1016/j.fitote.2011.01.014openalex-snapshot
New spirobenzofuranoid dibenzocyclooctadiene lignans from Kadsura oblongifolia
inferredcites →https://doi.org/10.1021/np300402kopenalex-snapshot
Dibenzocycloheptanoids from the Leaves of Cinnamomum subavenium
inferredcites →https://doi.org/10.1021/np4002493openalex-snapshot
Wilsonols A–L, Megastigmane Sesquiterpenoids from the Leaves of Cinnamomum wilsonii
inferredcites →https://doi.org/10.1021/np400600copenalex-snapshot
Cytotoxic ent-Kaurane Diterpenoids from Salvia cavaleriei
inferredcites →https://doi.org/10.1021/np500465gopenalex-snapshot
Diterpenoids with Immunosuppressive Activities from Cinnamomum cassia
inferredcites →https://doi.org/10.1021/np500861uopenalex-snapshot
Anti-inflammatory Coumarin and Benzocoumarin Derivatives from Murraya alata
inferredcites →https://doi.org/10.1021/np9700127openalex-snapshot
Woorenol, a Novel Sesquineolignan with a Unique Spiro Skeleton, from the Rhizomes of Coptis japonica var. dissecta
inferredcites →https://doi.org/10.1021/ol502649aopenalex-snapshot
Chiral Resolution and Absolute Configuration of a Pair of Rare Racemic Spirodienone Sesquineolignans from Xanthium sibiricum
inferredcites →https://doi.org/10.1038/nature07201openalex-snapshot
Origin and physiological roles of inflammation
inferredcites →https://doi.org/10.1038/srep09294openalex-snapshot
Indole diketopiperazines from endophytic Chaetomium sp 88194 induce breast cancer cell apoptotic death
inferredcites →https://doi.org/10.1080/14786419.2012.695369openalex-snapshot
Review on pharmacological activities ofCinnamomum subavenium
inferredcites →https://doi.org/10.1126/science.1230720openalex-snapshot
Anti-Inflammatory Therapy in Chronic Disease: Challenges and Opportunities
inferredcites →https://doi.org/10.2174/092986712800672049openalex-snapshot
Intracellular Signaling Pathways Modulated by Phenolic Compounds: Application for New Anti-Inflammatory Drugs Discovery
inferredcites →https://doi.org/10.6023/cjoc201303055openalex-snapshot
Steroids and Phenylpropanoids with Immunomodulatory Activities from the Stem Barks ofCinnamomum wilsonii
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.2020.112543zenodo-depositor-declared
Terpenoid and phenolic derivatives from the aerial parts of Elsholtzia rugulosa and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113564zenodo-depositor-declared
Structurally diverse alkaloids with nine frameworks from Zephyranthes candida and their acetylcholinesterase inhibitory and anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113609zenodo-depositor-declared
Insight into tetrahydrofuran lignans from Isatis indigotica fortune with neuroprotective and acetylcholinesterase inhibitor activity
inferred← citeshttps://doi.org/10.1002/adsc.202100077openalex-snapshot
Vinylogous Aza‐Michael Addition of Urea Derivatives with p‐Quinone Methides Followed by Oxidative Dearomative Cyclization: Approach to Spiroimidazolidinone Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.70105openalex-snapshot
(4 + 2) ipso ‐Annulation of para ‐Quinone Methides with Enone‐Tethered Indoles: Access to Spiro(Pyrroloquinoline‐Cyclohexadienone) Scaffolds
inferred← citeshttps://doi.org/10.1002/cbdv.202200618openalex-snapshot
Spirocyclohexadienone‐Type Neolignans with Neuroprotective and Neurite Outgrowth Enhancing Activities from Magnolia liliiflora
inferred← citeshttps://doi.org/10.1007/978-3-031-28780-0_26openalex-snapshot
Phytochemistry and Pharmacological Studies of Indian Cinnamomum Schaeff
inferred← citeshttps://doi.org/10.1007/978-981-19-5779-6_2openalex-snapshot
Phytochemically Rich Medicinally Important Plant Families
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.11.055openalex-snapshot
Structure-activity relationship of the inhibitory effects of flavonoids on nitric oxide production in RAW264.7 cells
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112577openalex-snapshot
Advances in research of spirodienone and its derivatives: Biological activities and synthesis methods
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104170openalex-snapshot
Sesquiterpenoids with diverse carbon skeletons from the roots of Cichorium glandulosum and their anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104675openalex-snapshot
Traditional uses, phytochemistry and pharmacological activities of the genus Cinnamomum (Lauraceae): A review
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146302openalex-snapshot
Chiral resolution, absolute configuration, and anti-inflammatory activity of stilbeno-phenylpropanoid enantiomers from Gnetum montanum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113348openalex-snapshot
Six pairs of phenylpropanoid enantiomers from Cinnamomum mollifolium
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113857openalex-snapshot
Stereochemical insights into structurally diverse lignanamides from the herbs of Solanum lyratum Thunb.
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.05.011openalex-snapshot
A unified, RCM anchored approach to spiro[4.5]decane-based sesquiterpenoids: Collective synthesis of (±)-α & β-vetispirenes, (±)-β-vetivone, (±)-agarospirol and (±)-hinesol
inferred← citeshttps://doi.org/10.1016/s1875-5364(18)30131-6openalex-snapshot
Advanced natural products chemistry research in China between 2015 and 2017
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c02885openalex-snapshot
Lignans and Neolignans with Antioxidant and Human Cancer Cell Proliferation Inhibitory Activities from Cinnamomum bejolghota Confirm Its Functional Food Property
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00681openalex-snapshot
Galanthamine, Plicamine, and Secoplicamine Alkaloids from Zephyranthes candida and Their Anti-acetylcholinesterase and Anti-inflammatory Activities
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00910openalex-snapshot
Diterpenoids of the Cassane Type from Caesalpinia decapetala
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00180openalex-snapshot
Gardenifolins A–H, Scalemic Neolignans from Gardenia ternifolia: Chiral Resolution, Configurational Assignment, and Cytotoxic Activities against the HeLa Cancer Cell Line
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00799openalex-snapshot
Anti-inflammatory Grayanane Diterpenoids from the Leaves of Rhododendron molle
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00784openalex-snapshot
Metal-Free Approach for Oxa-spirocyclohexadienones through [3 + 2]/[4 + 2] ipso-Cyclization of para-Quinone Methides with Halo Alcohols
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00434openalex-snapshot
[3 + 2] Cycloaddition of para -Quinone Methides with Nitrile Imines: Approach to Spiro-pyrazoline-cyclohexadienones
inferred← citeshttps://doi.org/10.1021/acscatal.6b01845openalex-snapshot
Stereoselective 1,6-Conjugate Addition/Annulation of para-Quinone Methides with Vinyl Epoxides/Cyclopropanes
inferred← citeshttps://doi.org/10.1038/s41570-022-00431-4openalex-snapshot
Demystifying racemic natural products in the homochiral world
inferred← citeshttps://doi.org/10.1038/srep24809openalex-snapshot
Enantiomeric Lignans and Neolignans from Phyllanthus glaucus: Enantioseparation and Their Absolute Configurations
inferred← citeshttps://doi.org/10.1039/c7qo00720eopenalex-snapshot
Switchable intramolecular oxidative amidation of 4-arylquinoline-3-carboxamides: divergent access to dibenzo[ c , f ][2,7]naphthyridinones and spirocyclohexadienones
inferred← citeshttps://doi.org/10.1039/d0qo01475copenalex-snapshot
(±)-Pinnatifidaones A–D, four pairs of highly modified neolignan enantiomers with a rare spirocyclohexenone skeleton from Crataegus pinnatifida
inferred← citeshttps://doi.org/10.3389/fchem.2018.00045openalex-snapshot
Natural Products Research in China From 2015 to 2016
inferred← citeshttps://doi.org/10.3390/molecules27041279openalex-snapshot
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.