On the public citation graph

Synthesis of the Oxepinochromone Natural Products Ptaeroxylin (Desoxykarenin), Ptaeroxylinol, and Eranthin

https://doi.org/10.1021/jo902117e
0 signed · 94 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/anie.200702363openalex-snapshot
Cascade Reactions Involving Formal [2+2] Thermal Cycloadditions: Total Synthesis of Artochamins F, H, I, and J
inferredcites →https://doi.org/10.1002/cber.19811140235openalex-snapshot
Neue Chromone aus Cneoraceen
inferredcites →https://doi.org/10.1002/ejoc.200600414openalex-snapshot
Total Synthesis of the Cytotoxic Guaipyridine Sesquiterpene Alkaloid (+)‐Cananodine
inferredcites →https://doi.org/10.1002/hlca.19910740318openalex-snapshot
4H‐Chromenone Glycosides from Eranthis hyemalis (L.) S ALISBURY
inferredcites →https://doi.org/10.1007/bf03049175openalex-snapshot
Nuclear oxidation in flavones and related compounds
inferredcites →https://doi.org/10.1016/j.tet.2009.05.027openalex-snapshot
Total synthesis of radulanin H and proposed structure of radulanin E
inferredcites →https://doi.org/10.1016/j.tetlet.2003.11.098openalex-snapshot
Synthesis of heliannuol D, an allelochemical from Helianthus annus
inferredcites →https://doi.org/10.1016/j.tetlet.2005.02.053openalex-snapshot
Total synthesis of (±)-heliannuol C and E via aromatic Claisen rearrangement
inferredcites →https://doi.org/10.1016/s0031-9422(00)82743-0openalex-snapshot
Eranthin und eranthin-β-D-glucosid: zwei neue chromone aus Eranthis hiemalis
inferredcites →https://doi.org/10.1016/s0040-4020(02)01658-7openalex-snapshot
Efficient entry to 1-benzoxepine ring skeleton via tandem SN2/Wittig reaction. Total synthesis of NADH: ubiquinone oxidoreductase (complex I) antagonist pterulinic acid
inferredcites →https://doi.org/10.1016/s0040-4020(03)00134-0openalex-snapshot
Synthesis of heliannane skeletons. Facile preparation of (±)-heliannuol D
inferredcites →https://doi.org/10.1016/s0040-4039(00)00676-6openalex-snapshot
A new preparation of 2,5-dihydro-1-benzoxepins using Mitsunobu cyclization, and the synthesis of natural radulanins
inferredcites →https://doi.org/10.1016/s0040-4039(01)01580-5openalex-snapshot
Total synthesis of NADH:ubiquinone oxidoreductase (complex I) antagonist pterulone and its analogue
inferredcites →https://doi.org/10.1016/s0040-4039(01)89821-xopenalex-snapshot
Chromones, containing an oxepin ring, from
inferredcites →https://doi.org/10.1016/s0065-2725(08)60644-3openalex-snapshot
Claisen Rearrangements in Heteroaromatic Systems
inferredcites →https://doi.org/10.1021/cr0200872openalex-snapshot
Synthesis of Oxygen- and Nitrogen-Containing Heterocycles by Ring-Closing Metathesis
inferredcites →https://doi.org/10.1021/jo050550lopenalex-snapshot
Synthesis of Two Naturally Occurring 3-Methyl-2,5-dihydro-1-benzoxepin Carboxylic Acids
inferredcites →https://doi.org/10.1021/jo980299sopenalex-snapshot
Connecting Directed Ortho Metalation and Olefin Metathesis Strategies. Benzene-Fused Multiring-Sized Oxygen Heterocycles. First Syntheses of Radulanin A and Helianane
inferredcites →https://doi.org/10.1039/b003553jopenalex-snapshot
Enantioselective total synthesis of heliannuols D and A †
inferredcites →https://doi.org/10.1039/b306356aopenalex-snapshot
Efficient syntheses of pterulone, pterulone B and related analogues
inferredcites →https://doi.org/10.1039/j39660000114openalex-snapshot
Extractives from East African timbers. Part II. Ptæroxylon obliquum
inferredcites →https://doi.org/10.1039/j39670000145openalex-snapshot
Constituents of sneezewood, Ptaeroxylon obliquum(Thunb.) Radlk. Part I. Chromones
inferredcites →https://doi.org/10.1039/p19750001776openalex-snapshot
Isolation of 5,7-dihydroxy-2-methylchromone and its 7-O-glycosides from Adina rubescens
inferredcites →https://doi.org/10.1039/p19880001417openalex-snapshot
Rhodium carbenoid mediated cyclisations. Part 2. Synthesis of cyclic ethers
inferredcites →https://doi.org/10.1039/p19890000721openalex-snapshot
Rhodium carbenoid mediated cyclisations. Part 3. Synthesis of cyclic ethers from lactones
inferredcites →https://doi.org/10.1055/s-2006-950398openalex-snapshot
Sequential Double Claisen Rearrangement and Two-Directional Ring-Closing Metathesis as a Route to Various Benzofused Bisoxepin and Bisoxocin Derivatives
inferredcites →https://doi.org/10.1080/00397919608003823openalex-snapshot
Total Synthesis of (±)-Calanolide A
inferredcites →https://doi.org/10.7164/antibiotics.50.325openalex-snapshot
Pterulinic Acid and Pterulone, Two Novel Inhibitors of NADH: Ubiquinone Oxidoreductase (Complex I) Produced by a Pterula Species. I. Production, Isolation and Biological Activities.
inferredcites →https://doi.org/10.7164/antibiotics.50.330openalex-snapshot
Pterulinic Acid and Pterulone, Two Novel Inhibitors of NADH: Ubiquinone Oxidoreductase (Complex I) Produced by a Pterla Species. II. Physico-chemical Properties and Structure Elucidationt.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4670489openalex-extracted
inferred← citeshttps://doi.org/10.1002/0471264180.or089.01openalex-snapshot
Olefin Ring‐Closing Metathesis
inferred← citeshttps://doi.org/10.1002/ange.201700890openalex-snapshot
Catalytic Enantioselective Synthesis of 2,5‐Dihydrooxepines
inferred← citeshttps://doi.org/10.1002/anie.201700890openalex-snapshot
Catalytic Enantioselective Synthesis of 2,5‐Dihydrooxepines
inferred← citeshttps://doi.org/10.1002/aoc.6555openalex-snapshot
Exciting progress in the transition metal‐catalyzed synthesis of oxepines, benzoxepines, dibenzoxepines, and other derivatives
inferred← citeshttps://doi.org/10.1002/cbdv.202200507openalex-snapshot
Natural Compounds with Oxepinochromene Scaffold. Structure, Source, Biological Activity and Synthesis
inferred← citeshttps://doi.org/10.1002/chem.201002757openalex-snapshot
Regioselectivity of the Claisen Rearrangement in meta ‐Allyloxy Aryl Ketones: An Experimental and Computational Study, and Application in the Synthesis of ( R )‐(−)‐Pestalotheol D
inferred← citeshttps://doi.org/10.1002/ejoc.201500374openalex-snapshot
Silver Triflate Catalyzed Cyclopropyl Carbinol Rearrangement for Benzo[b]oxepine and 2H‐Chromene Synthesis
inferred← citeshttps://doi.org/10.1002/ejoc.201501151openalex-snapshot
Tandem Claisen Rearrangement/6‐ endo Cyclization Approach to Allylated and Prenylated Chromones
inferred← citeshttps://doi.org/10.1002/ejoc.201900474openalex-snapshot
Iodocyclization of Propargyl Alcohols: Highly Facile Approach to Hetero/Carbocyclic Iodides
inferred← citeshttps://doi.org/10.1002/ejoc.202300968openalex-snapshot
Electrochemical Selenylation of Alkynyl Aryl Ketones: Efficient Synthesis of 3‐Selenylated Chromones under Catalyst‐ and Chemical‐Oxidant‐Free Conditions
inferred← citeshttps://doi.org/10.1002/hlca.201600028openalex-snapshot
Synthesis of Diverse Oxa‐Carbocycle‐Annulated Flavones Using the Combined Claisen Rearrangement and Ring‐Closing Metathesis
inferred← citeshttps://doi.org/10.1002/slct.201804029openalex-snapshot
Reductive Heck Reaction: An Emerging Alternative in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1007/978-3-642-41470-1_1openalex-snapshot
Synthesis of Seven-Membered Ring Ethers and Lactones
inferred← citeshttps://doi.org/10.1007/s10593-018-2322-yopenalex-snapshot
Convenient synthesis of 12-methyl[1]benzoxepino[3,4-b]quinolin-13(6H)-ones
inferred← citeshttps://doi.org/10.1016/b978-0-08-096805-6.00016-4openalex-snapshot
Seven-Membered Rings
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00530-9openalex-snapshot
5.29 Ring-Closing Metathesis
inferred← citeshttps://doi.org/10.1016/b978-0-323-89812-6.00016-xopenalex-snapshot
Seven-membered rings
inferred← citeshttps://doi.org/10.1016/j.ccr.2012.02.015openalex-snapshot
The chemistry of the carbon–transition metal double and triple bond: Annual survey covering the year 2010
inferred← citeshttps://doi.org/10.1016/j.gresc.2021.12.003openalex-snapshot
Synthesis of 3-thiocyanated chromones via TCCA/NH4SCN-mediated cyclization/thiocyanation of alkynyl aryl ketones
inferred← citeshttps://doi.org/10.1016/j.gresc.2024.01.002openalex-snapshot
Controlled generation of ortho-quinone methides and (4+3) cyclization with 2-indolylalcohols by dual photoredox/Brønsted acid relay catalysis
inferred← citeshttps://doi.org/10.1016/j.jare.2023.11.016openalex-snapshot
HIF-1α inhibition by MO-2097, a novel chiral-free benzofuran targeting hnRNPA2B1
inferred← citeshttps://doi.org/10.1016/j.jep.2021.114365openalex-snapshot
Anthelmintic, antimycobacterial, antifungal, larvicidal and cytotoxic activities of acetone leaf extracts, fractions and isolated compounds from Ptaeroxylon obliquum (Rutaceae)
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2024.115743openalex-snapshot
Chromone-based fluorescent probe for peroxynitrite imaging in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.tet.2013.06.003openalex-snapshot
The Claisen rearrangement in the syntheses of bioactive natural products
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.06.070openalex-snapshot
A reductive Mizoroki–Heck approach to dibenzo[b,e]oxepine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.07.003openalex-snapshot
Synthesis of benzoxepinopyrrolidines/spiropyrrolidines via oxa-Pictet–Spengler and [3+2] cycloaddition reactions
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00587openalex-snapshot
Synthesis and Antifungal Activity of Chromones and Benzoxepines from the Leaves of Ptaeroxylon obliquum
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00361openalex-snapshot
Propargyl Chalcones’ Radical Annulation/Sulfonation Reaction: Efficient Synthesis of Benzo[ b ]oxepin-5(2 H )-one and Chromane Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00446openalex-snapshot
Regio- and Diastereoselective Construction of Functionalized Benzo[b]oxepines and Benzo[b]azepines via Recyclable Gold(I)-Catalyzed Cyclizations
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00567openalex-snapshot
Electrocatalytic Cascade Selenylation/Cyclization/Deamination of 2-Hydroxyaryl Enaminones: Synthesis of 3-Selenylated Chromones under Mild Conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00583openalex-snapshot
One-Pot Synthesis of 5-Amino-2,5-dihydro-1-benzoxepines: Access to Pharmacologically Active Heterocyclic Scaffolds
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02413openalex-snapshot
Regiospecific Synthesis of Benzoxepines through Pd-Catalyzed Carbene Migratory Insertion and C–C Bond Cleavage
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02789openalex-snapshot
Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02880openalex-snapshot
Synthesis of CBD and Its Derivatives Bearing Various C4′-Side Chains with a Late-Stage Diversification Method
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03279openalex-snapshot
Asymmetric [4 + 3] Annulations for Constructing Divergent Oxepane Frameworks via Cooperative Tertiary Amine/Transition Metal Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00893openalex-snapshot
Phosphine-Mediated [4 + 3] Annulation of Diynoates and 2-Arylidene Indane-1,3-diones: Access of Indeno[1,2- b ]oxepin-4-ylidenes and Beyond
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00801openalex-snapshot
Direct Access to Trifluoromethylated Benzo[d]oxepines from o-Alkynylaryl Aldehydes and Trifluorodiazoethane
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03709openalex-snapshot
Lewis Base-Catalyzed [4 + 3] Annulation of ortho-Quinone Methides and MBH Carbonates: Synthesis of Functionalized Benzo[b]oxepines Bearing Oxindole Scaffolds
inferred← citeshttps://doi.org/10.1021/acscatal.2c02667openalex-snapshot
Recent Advancement in Palladium-Catalyzed C–C Bond Activation of Strained Ring Systems: Three- and Four-Membered Carbocycles as Prominent C3/C4 Building Blocks
inferred← citeshttps://doi.org/10.1021/jo401799fopenalex-snapshot
Toward a Synthesis of Hirsutellone B by the Concept of Double Cyclization
inferred← citeshttps://doi.org/10.1021/jo502571ropenalex-snapshot
TMSI-Promoted Vinylogous Michael Addition of Siloxyfuran to 2-Substituted Chromones: A General Approach for the Total Synthesis of Chromanone Lactone Natural Products
inferred← citeshttps://doi.org/10.1021/ol302252hopenalex-snapshot
Gold-Catalyzed Cyclizations of (o-Alkynyl)phenoxyacrylates with External Nucleophiles: Regio- and Stereoselective Synthesis of Functionalized Benzo[b]oxepines
inferred← citeshttps://doi.org/10.1021/ol303482kopenalex-snapshot
Total Synthesis of Chaetoquadrins A–C
inferred← citeshttps://doi.org/10.1039/c3ob41624kopenalex-snapshot
FeCl 3 -catalyzed synthesis of functionally diverse dibenzo[b,f]oxepines and benzo[b]oxepines via alkyne–aldehyde metathesis
inferred← citeshttps://doi.org/10.1039/c4ob01743aopenalex-snapshot
Lewis acid promoted construction of chromen-4-one and isoflavone scaffolds via regio- and chemoselective domino Friedel–Crafts acylation/Allan–Robinson reaction
inferred← citeshttps://doi.org/10.1039/c8sc03697gopenalex-snapshot
Dalmanol biosyntheses require coupling of two separate polyketide gene clusters
inferred← citeshttps://doi.org/10.1039/d0qo01175dopenalex-snapshot
Metal-free synthesis of 3-chalcogenyl chromones from alkynyl aryl ketones and diorganyl diselenides/disulfides mediated by PIFA
inferred← citeshttps://doi.org/10.1039/d2ob00696kopenalex-snapshot
Silver-catalysed three-component reactions of alkynyl aryl ketones, element selenium, and boronic acids leading to 3-organoselenylchromones
inferred← citeshttps://doi.org/10.1039/d3ob00077jopenalex-snapshot
Base-promoted cyclization of ortho -hydroxyacetophenones with in situ generated cyclopropenes: diastereoselective access to spirobenzo[ b ]oxepines and related precursors
inferred← citeshttps://doi.org/10.1055/a-1509-6078openalex-snapshot
Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones
inferred← citeshttps://doi.org/10.1055/s-0037-1610776openalex-snapshot
Total Synthesis of Oxepin and Dihydrooxepin Containing Natural Products
inferred← citeshttps://doi.org/10.1055/s-0042-1751361openalex-snapshot
Protecting-Group-Free Synthesis of Novel Cannabinoid-Like 2,5-Dihydrobenzoxepines
inferred← citeshttps://doi.org/10.1080/10406638.2012.663450openalex-snapshot
Synthesis of Polycyclic-fused Heterocycles Combining Both Quinoline Ring and Benzoxepine Framework in A Single Molecule
inferred← citeshttps://doi.org/10.1080/14786419.2014.998216openalex-snapshot
Triglyceride accumulation inhibitory effects of new chromone glycosides from Drynaria fortunei
inferred← citeshttps://doi.org/10.1088/1742-6596/2603/1/012058openalex-snapshot
Synthesis of 7-Membered Heterocyclic Compounds and Their Biological Activity
inferred← citeshttps://doi.org/10.21577/1984-6835.20170094openalex-snapshot
The most Used Claisen Rearrangements in Organic Synthesis: A Review
inferred← citeshttps://doi.org/10.2174/1570180814666161227125227openalex-snapshot
A Brief Overview on Chemistry and Biology of Benzoxepine
inferred← citeshttps://doi.org/10.2174/2213335607666200226101602openalex-snapshot
Microwave-mediated Synthesis of Medium Ring-sized Heterocyclic Compounds
inferred← citeshttps://doi.org/10.24820/ark.5550190.p010.547openalex-snapshot
Synthesis and anti-proliferative activity of novel oxepin-annulated coumarins
inferred← citeshttps://doi.org/10.3390/molecules17010191openalex-snapshot
Chromone and Flavonoid Alkaloids: Occurrence and Bioactivity
inferred← citeshttps://doi.org/10.3390/molecules21081032openalex-snapshot
Microwave-Assisted Syntheses of Bioactive Seven-Membered, Macro-Sized Heterocycles and Their Fused Derivatives
inferred← citeshttps://doi.org/10.3390/plants12223795openalex-snapshot
The Genus Eranthis: Prospects of Research on Its Phytochemistry, Pharmacology, and Biotechnology
inferred← citeshttps://doi.org/10.3390/plants14121746openalex-snapshot
A Review of the Ethnomedicine, Phytochemistry, Pharmacology and Toxicological Studies on Ptaeroxylon obliquum (Thunb.) Radlk. (Rutaceae)
inferred← citeshttps://doi.org/10.3987/com-12-s(n)89openalex-snapshot
DIVERSITY ORIENTED APPROACH TO 9-ARYL-SUBSTITUTED NAPHTHOXEPINE DERIVATIVES VIA CLAISEN REARRANGEMENT, RING-CLOSING METATHESIS AND SUZUKI–MIYAURA CROSS-COUPLING AS KEY STEPS
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.