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Hopeahainol A: An Acetylcholinesterase Inhibitor from Hopea hainanensis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Oral physostigmine and lecithin improve memory in Alzheimer disease
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Hopeanol: A Potent Cytotoxin with A Novel Skeleton from Hopea exalata
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New Resveratrol Oligomers from the Stem Bark of Hopea hainanensis
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Frequency dependent nonlinear optical properties of molecules: Formulation and implementation in the HONDO program
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A new and rapid colorimetric determination of acetylcholinesterase activity
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Enzyme Kinetics: Behaviour and Analysis of Rapid Equilibrium and Steady-State Enzyme Systems
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Two new oligostilbenes with dihydrobenzofuran from the stem bark of Vateria indica
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Four Novel Oligostilbenes from the Roots of Vitis amurensis
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Crystal Structures of Acetylcholinesterase in Complex with Organophosphorus Compounds Suggest that the Acyl Pocket Modulates the Aging Reaction by Precluding the Formation of the Trigonal Bipyramidal Transition State,
inferredcites →https://doi.org/10.1021/ja973690oopenalex-snapshot
Theory-Assisted Determination of Absolute Stereochemistry for Complex Natural Products via Computation of Molar Rotation Angles
inferredcites →https://doi.org/10.1021/np060242yopenalex-snapshot
Bioactive Oligostilbenoids from the Stem Bark of Hopea exalata
inferredcites →https://doi.org/10.1021/ol035560sopenalex-snapshot
Sieboldine A, a Novel Tetracyclic Alkaloid from Lycopodium sieboldii, Inhibiting Acetylcholinesterase
inferredcites →https://doi.org/10.1021/ol062307uopenalex-snapshot
Vibralactone: A Lipase Inhibitor with an Unusual Fused β-Lactone Produced by Cultures of the Basidiomycete Boreostereum vibrans
inferredcites →https://doi.org/10.1038/nsb0197-57openalex-snapshot
Structure of acetylcholinesterase complexed with the nootropic alkaloid, (–)-huperzine A
inferredcites →https://doi.org/10.1063/1.464913openalex-snapshot
Density-functional thermochemistry. III. The role of exact exchange
inferredcites →https://doi.org/10.1074/jbc.274.43.30370openalex-snapshot
Conformational Flexibility of the Acetylcholinesterase Tetramer Suggested by X-ray Crystallography
inferredcites →https://doi.org/10.1107/s0907444902011642openalex-snapshot
Structure of a complex of the potent and specific inhibitor BW284C51 withTorpedo californicaacetylcholinesterase
inferredcites →https://doi.org/10.1126/science.7058341openalex-snapshot
Alzheimer's Disease and Senile Dementia: Loss of Neurons in the Basal Forebrain
inferredcites →https://doi.org/10.1176/ajp.139.11.1421openalex-snapshot
Enhancement of memory processes in Alzheimer's disease with multiple- dose intravenous physostigmine
inferredcites →https://doi.org/10.1176/ajp.139.6.838openalex-snapshot
Apomorphine and Other Dopaminomimetics: Basic Pharmacology, Vol. I
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Stilbenes: Source plants, chemistry, biosynthesis, pharmacology, application and problems related to their clinical Application-A comprehensive review
inferred← citeshttps://doi.org/10.1002/9781118299753.ch13openalex-snapshot
Strategies for the Controlled Synthesis of Oligomeric Polyphenols
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Lignans, Lignins, and Resveratrols
inferred← citeshttps://doi.org/10.1002/9783527634606.ch19openalex-snapshot
Synthetic Approaches to the Resveratrol‐Based Family of Oligomeric Natural Products
inferred← citeshttps://doi.org/10.1002/adsc.201301038openalex-snapshot
Catalytic Asymmetric Synthesis of Chiral Benzofuranones
inferred← citeshttps://doi.org/10.1002/ange.200900438openalex-snapshot
Total Synthesis of Hopeahainol A and Hopeanol
inferred← citeshttps://doi.org/10.1002/ange.201000044openalex-snapshot
Pflanzliche Polyphenole: chemische Eigenschaften, biologische Aktivität und Synthese
inferred← citeshttps://doi.org/10.1002/ange.201100283openalex-snapshot
Enantioselective Base‐Free Electrophilic Amination of Benzofuran‐2(3H)‐ones: Catalysis by Binol‐Derived P‐Spiro Quaternary Phosphonium Salts
inferred← citeshttps://doi.org/10.1002/ange.201107730openalex-snapshot
Total Syntheses of Hopeanol and Hopeahainol A Empowered by a Chiral Brønsted Acid Induced Pinacol Rearrangement
inferred← citeshttps://doi.org/10.1002/ange.201303099openalex-snapshot
Palladium(II)‐Catalyzed Dehydrogenative Cross‐Coupling between Two CH Bonds: Unexpected CC Bond Formation
inferred← citeshttps://doi.org/10.1002/ange.201601028openalex-snapshot
Asymmetric Conjugate Addition of Benzofuran‐2‐ones to Alkyl 2‐Phthalimidoacrylates: Modeling Structure–Stereoselectivity Relationships with Steric and Electronic Parameters
inferred← citeshttps://doi.org/10.1002/anie.200900438openalex-snapshot
Total Synthesis of Hopeahainol A and Hopeanol
inferred← citeshttps://doi.org/10.1002/anie.201000044openalex-snapshot
Plant Polyphenols: Chemical Properties, Biological Activities, and Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201100283openalex-snapshot
Enantioselective Base‐Free Electrophilic Amination of Benzofuran‐2(3H)‐ones: Catalysis by Binol‐Derived P‐Spiro Quaternary Phosphonium Salts
inferred← citeshttps://doi.org/10.1002/anie.201107730openalex-snapshot
Total Syntheses of Hopeanol and Hopeahainol A Empowered by a Chiral Brønsted Acid Induced Pinacol Rearrangement
inferred← citeshttps://doi.org/10.1002/anie.201303099openalex-snapshot
Palladium(II)‐Catalyzed Dehydrogenative Cross‐Coupling between Two CH Bonds: Unexpected CC Bond Formation
inferred← citeshttps://doi.org/10.1002/anie.201601028openalex-snapshot
Asymmetric Conjugate Addition of Benzofuran‐2‐ones to Alkyl 2‐Phthalimidoacrylates: Modeling Structure–Stereoselectivity Relationships with Steric and Electronic Parameters
inferred← citeshttps://doi.org/10.1002/asia.201201244openalex-snapshot
Synthesis of Optically Enriched Spirocyclic Benzofuran‐2‐ones by Bifunctional Thiourea‐Base Catalyzed Double‐Michael Addition of Benzofuran‐2‐ones to Dienones
inferred← citeshttps://doi.org/10.1002/asia.201600873openalex-snapshot
A Convenient Palladium‐Catalyzed Carbonylative Synthesis of Benzofuran‐2(3 H)‐ones with Formic Acid as the CO Source
inferred← citeshttps://doi.org/10.1002/cbdv.201300349openalex-snapshot
Halogenated Metabolites Isolated from Penicillium citreonigrum
inferred← citeshttps://doi.org/10.1002/chem.200801000openalex-snapshot
Cephalosol: An Antimicrobial Metabolite with an Unprecedented Skeleton from Endophytic Cephalosporium acremonium IFB‐E007
inferred← citeshttps://doi.org/10.1002/chem.201000230openalex-snapshot
Immunosuppressive Resveratrol Aneuploids from Hopea chinensis
inferred← citeshttps://doi.org/10.1002/chem.201104078openalex-snapshot
Relative and Absolute Configuration of Vatiparol (1 mg): A Novel Anti‐inflammatory Polyphenol
inferred← citeshttps://doi.org/10.1002/chem.202401303openalex-snapshot
Electrochemical Oxidation Enables Radical Dearomative Spiroannulation to 2H‐Spiro[benzofuran‐3,9′‐fluoren]‐2‐one
inferred← citeshttps://doi.org/10.1002/chin.200820214openalex-snapshot
ChemInform Abstract: Hopeahainol A: An Acetylcholinesterase Inhibitor from Hopea hainanensis.
inferred← citeshttps://doi.org/10.1002/chir.22124openalex-snapshot
The Effect of Stereochemistry on the Biological Activity of Natural Phytotoxins, Fungicides, Insecticides and Herbicides
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Organocatalytic Asymmetric Branching Sequence of MBH Carbonates: Access to Chiral Benzofuran‐2(3H)‐one Derivatives with Three Stereocenters
inferred← citeshttps://doi.org/10.1002/cjoc.201400463openalex-snapshot
A Concise Synthesis of 2‐(2‐Hydroxyphenyl)acetonitriles via the o‐Quinone Methides Generated from 2‐(1‐Tosylalkyl)phenols
inferred← citeshttps://doi.org/10.1002/ejoc.200901245openalex-snapshot
Trichiliton A, a Novel Limonoid from Trichilia connaroides
inferred← citeshttps://doi.org/10.1002/ejoc.201100414openalex-snapshot
Daphmalenines A and B: Two New Alkaloids with Unusual Skeletons from Daphniphyllum himalense
inferred← citeshttps://doi.org/10.1002/ejoc.201100941openalex-snapshot
Regiolone and Isosclerone, Two Enantiomeric Phytotoxic Naphthalenone Pentaketides: Computational Assignment of Absolute Configuration and Its Relationship with Phytotoxic Activity
inferred← citeshttps://doi.org/10.1002/ejoc.201101765openalex-snapshot
Asymmetric Michael Addition Reactions between 3‐Substituted Benzofuran‐2(3H)‐ones and 1,1‐Bis(phenylsulfonyl)ethylene Catalyzed by Bifunctional Catalysts Containing Tertiary Amine and Thiourea Groups
inferred← citeshttps://doi.org/10.1002/ejoc.201301686openalex-snapshot
Catalytic Friedel–Crafts/Lactonization Domino Reaction: Facile Access to 3‐Hydroxybenzofuran‐2‐one Scaffold
inferred← citeshttps://doi.org/10.1002/ejoc.201600138openalex-snapshot
Transition‐Metal‐Catalyzed Acyloxylation: Activation of C(sp2)–H and C(sp3)–H Bonds
inferred← citeshttps://doi.org/10.1002/ejoc.201801080openalex-snapshot
Gold(I)‐Catalyzed and Nucleophile‐Guided Ligand‐Directed Divergent Synthesis
inferred← citeshttps://doi.org/10.1002/ejoc.201900439openalex-snapshot
Heterocycle Synthesis through Pd‐Catalyzed Carbonylative Coupling
inferred← citeshttps://doi.org/10.1007/s11418-020-01412-xopenalex-snapshot
Resveratrol oligomer structure in Dipterocarpaceaeous plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-824021-2.00003-0openalex-snapshot
Applications of Pictet–Spengler reaction in the total synthesis of alkaloids
inferred← citeshttps://doi.org/10.1016/b978-0-323-91097-2.00006-6openalex-snapshot
Bioactive stilbenes from plants
inferred← citeshttps://doi.org/10.1016/b978-0-444-59530-0.00008-3openalex-snapshot
Novel Plant-Derived Biomedical Agents and Their Biosynthetic Origin
inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00033-2openalex-snapshot
Terrestrial Plants as a Source of Novel Pharmaceutical Agents
inferred← citeshttps://doi.org/10.1016/j.antiviral.2012.05.001openalex-snapshot
Inhibition of herpes simplex virus infection by oligomeric stilbenoids through ROS generation
inferred← citeshttps://doi.org/10.1016/j.cbi.2016.05.032openalex-snapshot
Hopeahainol A binds reversibly at the acetylcholinesterase (AChE) peripheral site and inhibits enzyme activity with a novel higher order concentration dependence
inferred← citeshttps://doi.org/10.1016/j.cclet.2019.06.015openalex-snapshot
Highly efficient enantioselective synthesis of bispiro[benzofuran-oxindole/benzofuran-chromanone]s through organocatalytic inter-/intramolecular Michael cycloaddition
inferred← citeshttps://doi.org/10.1016/j.ejphar.2009.07.011openalex-snapshot
Construction of drug screening cell model and application to new compounds inhibiting FITC-fibrinogen binding to CHO cells expressing human αIIbβ3
inferred← citeshttps://doi.org/10.1016/j.etap.2009.01.009openalex-snapshot
Protective effect of hopeahainol A, a novel acetylcholinesterase inhibitor, on hydrogen peroxide-induced injury in PC12 cells
inferred← citeshttps://doi.org/10.1016/j.fitote.2011.11.009openalex-snapshot
Anti-acetylcholinesterase, anti-α-glucosidase, anti-leishmanial and anti-fungal activities of chemical constituents of Beilschmiedia species
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104502openalex-snapshot
Shoreanol A and B, unprecedented oligostilbenoids from the twigs of Shorea obtusa Wall
inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107476openalex-snapshot
Stilbenoids from the bark of Hopea odorata: antioxidant and antidiabetic activities
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115351openalex-snapshot
Copper-catalyzed regioselective C−H alkylation of phenol derivatives with unactivated alkyl chlorides: Manifesting a Cu(I)/Cu(III) pathway
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2013.03.007openalex-snapshot
P-Spiro phosphonium salts catalyzed asymmetric fluorination of 3-substituted benzofuran-2(3H)-ones
inferred← citeshttps://doi.org/10.1016/j.jpba.2010.01.047openalex-snapshot
Assignment of the absolute configuration at the sulfur atom of thioridazine metabolites by the analysis of their chiroptical properties: The case of thioridazine 2-sulfoxide
inferred← citeshttps://doi.org/10.1016/j.jpba.2025.116669openalex-snapshot
Cellulose filter paper immobilized acetylcholinesterase for rapid screening of enzyme inhibitors in Phyllanthus emblica L.
inferred← citeshttps://doi.org/10.1016/j.microc.2021.106438openalex-snapshot
Screening and identification of acetylcholinesterase inhibitors from Terminalia chebula fruits based on ultrafiltration and ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.phytol.2018.04.014openalex-snapshot
Bioactive aromatic metabolites from the sea urchin-derived actinomycete Streptomyces spectabilis strain HDa1
inferred← citeshttps://doi.org/10.1016/j.steroids.2014.12.002openalex-snapshot
Bioactive steroidal alkaloids from Buxus macowanii Oliv.
inferred← citeshttps://doi.org/10.1016/j.taap.2012.12.017openalex-snapshot
Vaticaffinol, a resveratrol tetramer, exerts more preferable immunosuppressive activity than its precursor in vitro and in vivo through multiple aspects against activated T lymphocytes
inferred← citeshttps://doi.org/10.1016/j.tet.2015.04.114openalex-snapshot
Asymmetric addition of 3-substituted benzofuran-2-ones to isatin N-Boc ketimines catalyzed by chiral biscinchona alkaloid catalyst
inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.10.028openalex-snapshot
The absolute configuration of simple aliphatic alcohols through a chemical/computational approach: triarylether derivatives of (+)-endo-2-norborneol as a case study
inferred← citeshttps://doi.org/10.1016/j.tetasy.2015.10.010openalex-snapshot
Ruthenium–Me-BIPAM-catalyzed addition reaction of aryl-boronic acids to benzofuran-2,3-diones for the enantioselective synthesis of 3-aryl-3-hydroxybenzofuran-2-ones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.08.023openalex-snapshot
Volvalerenone A, a new type of mononorsesquiterpenoid with an unprecedented 3,12-oxo bridge from Valeriana officinalis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.04.071openalex-snapshot
Organocatalytic asymmetric Michael addition of benzofuran-2(3H)-ones to alkylideneindolenines generated in situ from arenesulfonylalkylindoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.09.087openalex-snapshot
Asymmetric alkylation of 3-substituted benzofuran-2(3H)-ones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.04.111openalex-snapshot
Enantioselective synthesis of spirocyclic tetrahydrothiophene derivatives bearing a benzofuran-3(2H)-one scaffold. Unusual supramolecular crystal structure with high Z′
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151059openalex-snapshot
First total synthesis of rhuscholide A, glabralide B and denudalide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151396openalex-snapshot
Cobalt-catalyzed C H activation/C O formation: Synthesis of benzofuranones
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01583openalex-snapshot
TfOH-Catalyzed Cascade C–H Activation/Lactonization of Phenols with α-Aryl-α-diazoesters: Rapid Access to α-Aryl Benzofuranones
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00134openalex-snapshot
A Diastereoselective Assembly of Tetralone Derivatives via a Tandem Michael Reaction and ipso-Substitution of the Nitro Group
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01233openalex-snapshot
Direct Two Carbon Ring Expansion of 1-Indanones with Ynones: An Eco-Friendly, One-Flask Approach to Functionally Enriched 5H-Benzo[7]annulenes
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02864openalex-snapshot
Palladium(II)-Catalyzed Transformation of 3-Alkylbenzofurans to [2,3′-Bibenzofuran]-2′(3′H)-ones: Oxidative Dimerization of 3-Alkylbenzofurans
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01395openalex-snapshot
Catalytic Oxidation of 3-Arylbenzofuran-2(3H)-ones with PCC-H5IO6: Syntheses of 3-Aryl-3-hydroxy/3-amido-3-arylbenzofuran-2(3H)-ones
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01774openalex-snapshot
Organocatalytic Aza-Friedel–Crafts/Lactonization Domino Reaction of Naphthols and Phenols with 2-Acetamidoacrylate to Naphtho- and Benzofuranones Bearing a Quaternary Center at the C3 Position
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01076openalex-snapshot
Divergent Total Synthesis of Chaetoglines C to F
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03028openalex-snapshot
Phosphorous Acid-Catalyzed Alkylation of Phenols with Alkenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03059openalex-snapshot
Chiral Calcium Phosphate Catalyzed Enantioselective Amination of 3-Aryl-2-benzofuranones
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03014openalex-snapshot
Asymmetric Synthesis of Benzofuranones with a C3 Quaternary Center via an Addition/Cyclization Cascade Using Noncovalent N-Heterocyclic Carbene Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04342openalex-snapshot
Catalytic Asymmetric Desymmetrizing [4+2] Cycloaddition/Base-Mediated Oxidative Aromatization Sequence: De Novo Synthesis of Isobenzofuranone-Embedded Chiral Arenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02440openalex-snapshot
Catalytic Asymmetric Synthesis of 3-Hydroxy-3-trifluoromethyl Benzofuranones via Tandem Friedel–Crafts/Lactonization Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03865openalex-snapshot
Noncovalent N-Heterocyclic Carbene Catalysis Enables Asymmetric Conjugate Addition of 2-Benzofuranones to Terminal C-Electrophiles
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00163openalex-snapshot
Amination of 3-Substituted Benzofuran-2(3H)-ones Triggered by Single-Electron Transfer
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01482openalex-snapshot
Phosphine-Catalyzed Domino β/γ-Additions of Benzofuranones with Allenoates: A Method for Unsymmetrical 3,3-Disubstituted Benzofuranones
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02555openalex-snapshot
Asymmetric Rh(I)-Catalyzed Functionalization of the 3-C(sp3)–H Bond of Benzofuranones with α-Diazoesters
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03082openalex-snapshot
Rhodium(III)-Catalyzed Redox-Neutral Cascade [3 + 2] Annulation of N-Phenoxyacetamides with Propiolates via C–H Functionalization/Isomerization/Lactonization
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01058openalex-snapshot
Sequential Assembly of Morita–Baylis–Hillman Carbonates and Activated ortho-Vinylbenzaldehydes To Construct Chiral Methanobenzo[7]annulenone Frameworks
inferred← citeshttps://doi.org/10.1021/acscatal.8b03292openalex-snapshot
Design of Efficient Chiral Bifunctional Phase-Transfer Catalysts Possessing an Amino Functionality for Asymmetric Aminations
inferred← citeshttps://doi.org/10.1021/cr500689bopenalex-snapshot
Chemistry and Biology of Resveratrol-Derived Natural Products
inferred← citeshttps://doi.org/10.1021/cr9002402openalex-snapshot
Novel Syntheses of Bridge-Containing Organic Compounds
inferred← citeshttps://doi.org/10.1021/ja102623jopenalex-snapshot
Total Synthesis and Biological Evaluation of the Resveratrol-Derived Polyphenol Natural Products Hopeanol and Hopeahainol A
inferred← citeshttps://doi.org/10.1021/ja311259xopenalex-snapshot
Pd(II)-Catalyzed Enantioselective C–H Activation/C–O Bond Formation: Synthesis of Chiral Benzofuranones
inferred← citeshttps://doi.org/10.1021/ja312125aopenalex-snapshot
Exploiting the Modularity of Ion-Paired Chiral Ligands for Palladium-Catalyzed Enantioselective Allylation of Benzofuran-2(3H)-ones
inferred← citeshttps://doi.org/10.1021/jf900756dopenalex-snapshot
Antioxidant Oligostilbenoids from the Stem Wood of Hopea hainanensis
inferred← citeshttps://doi.org/10.1021/jo100401wopenalex-snapshot
Absolute Configuration through the DFT Simulation of the Optical Rotation. Importance of the Correct Selection of the Input Geometry: A Caveat
inferred← citeshttps://doi.org/10.1021/jo101832eopenalex-snapshot
Chiral Amine Thiourea-Promoted Enantioselective Michael Addition Reactions of 3-Substituted Benzofuran-2(3H)-ones to Maleimides
inferred← citeshttps://doi.org/10.1021/jo200557bopenalex-snapshot
Chiral Biscinchona Alkaloid Promoted Asymmetric Allylic Alkylation of 3-Substituted Benzofuran-2(3 H )-ones with Morita–Baylis–Hillman Carbonates
inferred← citeshttps://doi.org/10.1021/jo300395xopenalex-snapshot
Metal-Free Tandem Friedel–Crafts/Lactonization Reaction to Benzofuranones Bearing a Quaternary Center at C3 Position
inferred← citeshttps://doi.org/10.1021/jo402853vopenalex-snapshot
Enantioselective Desymmetrization of Diesters
inferred← citeshttps://doi.org/10.1021/np100494uopenalex-snapshot
Triterpenoidal Alkaloids fromBuxus natalensisand Their Acetylcholinesterase Inhibitory Activity
inferred← citeshttps://doi.org/10.1021/np800700eopenalex-snapshot
Bioactive Alkaloids from Endophytic Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1021/ol200878wopenalex-snapshot
Volvalerelactones A and B, Two New Sesquiterpenoid Lactones with an Unprecedented Skeleton from Valeriana officinalis var. latifolia
inferred← citeshttps://doi.org/10.1021/ol303569bopenalex-snapshot
Direct Lactonization of 2-Arylacetic Acids through Pd(II)-Catalyzed C–H Activation/C–O Formation
inferred← citeshttps://doi.org/10.1021/ol403094aopenalex-snapshot
Asymmetric Diels–Alder Reaction of 3-Olefinic Benzofuran-2-ones and Polyenals: Construction of Chiral Spirocyclic Benzofuran-2-ones
inferred← citeshttps://doi.org/10.1021/ol5031684openalex-snapshot
N-Heterocyclic Carbene Catalyzed Annulation of Enals to Aurone Analogs: Synthesis of Cyclopentene-Fused Spirobenzofuran-3-ones
inferred← citeshttps://doi.org/10.1021/ol9007958openalex-snapshot
Daphenylline, a New Alkaloid with an Unusual Skeleton, from Daphniphyllum longeracemosum
inferred← citeshttps://doi.org/10.1021/ol901631nopenalex-snapshot
Benzotrifuranone: Synthesis, Structure, and Access to Polycyclic Heteroaromatics
inferred← citeshttps://doi.org/10.1021/ol902262gopenalex-snapshot
Daphhimalenine A, a New Alkaloid with an Unprecedented Skeleton, from Daphniphyllum himalense
inferred← citeshttps://doi.org/10.1038/s41467-021-27546-4openalex-snapshot
Computation-guided asymmetric total syntheses of resveratrol dimers
inferred← citeshttps://doi.org/10.1039/c0cc01957gopenalex-snapshot
Multiple approaches to enantiopure spirocyclic benzofuranones using organocatalytic cascade reactions
inferred← citeshttps://doi.org/10.1039/c0np00027bopenalex-snapshot
Natural products as a source of Alzheimer's drug leads
inferred← citeshttps://doi.org/10.1039/c1ob06518aopenalex-snapshot
Asymmetric Michael addition reactions of 3-substituted benzofuran-2(3H)-ones to nitroolefins catalyzed by a bifunctional tertiary-amine thiourea
inferred← citeshttps://doi.org/10.1039/c1ra00007aopenalex-snapshot
Oligostilbenes from Vatica mangachapoi with xanthine oxidase and acetylcholinesterase inhibitory activities
inferred← citeshttps://doi.org/10.1039/c2cs35116aopenalex-snapshot
Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance
inferred← citeshttps://doi.org/10.1039/c2ob25694kopenalex-snapshot
Chiral phosphine-catalyzed asymmetric allylic alkylation of 3-substituted benzofuran-2(3H)-ones or oxindoles with Morita–Baylis–Hillman carbonates
inferred← citeshttps://doi.org/10.1039/c3ob27288eopenalex-snapshot
Phosphine-containing Lewis base catalyzed cyclization of benzofuranone type electron-deficient alkenes with allenoates: a facile synthesis of spirocyclic benzofuranones
inferred← citeshttps://doi.org/10.1039/c3ob41028eopenalex-snapshot
N-heterocyclic carbene catalyzed annulation of benzofuran-2,3-diones and enals: a concise synthesis of spiro-bis-lactone
inferred← citeshttps://doi.org/10.1039/c4cc01499eopenalex-snapshot
Highly diastereo- and enantioselective Michael addition of 3-substituted benzofuran-2(3H)-ones to 4-oxo-enoates catalyzed by lanthanide(iii) complexes
inferred← citeshttps://doi.org/10.1039/c5ob00258copenalex-snapshot
Facile synthesis of spirooxindole-pyrazolines and spirobenzofuranone-pyrazolines and their fungicidal activity
inferred← citeshttps://doi.org/10.1039/c5sc03135dopenalex-snapshot
Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones
inferred← citeshttps://doi.org/10.1039/c6cc07105hopenalex-snapshot
Organocatalytic asymmetric formal arylation of benzofuran-2(3H)-ones with cooperative visible light photocatalysis
inferred← citeshttps://doi.org/10.1039/c6cs00935bopenalex-snapshot
Recent applications of the 1,2-carbon atom migration strategy in complex natural product total synthesis
inferred← citeshttps://doi.org/10.1039/c6ob02782bopenalex-snapshot
Palladium-catalyzed carbonylative synthesis of benzofuran-2(3H)-ones from 2-hydroxybenzyl alcohols using formic acid as the CO source
inferred← citeshttps://doi.org/10.1039/c9gc00305copenalex-snapshot
Recyclable nickel-catalyzed C–H/O–H dual functionalization of phenols with mandelic acids for the synthesis of 3-aryl benzofuran-2(3 H )-ones under solvent-free conditions
inferred← citeshttps://doi.org/10.1039/c9ob01553aopenalex-snapshot
Rhodium( iii )-catalysed cascade [3 + 2] annulation of N -aryloxyacetamides with 3-(hetero)arylpropiolic acids: synthesis of benzofuran-2(3 H )-ones
inferred← citeshttps://doi.org/10.1039/c9qo00265kopenalex-snapshot
A bifunctional pyrazolone–chromone synthon directed organocatalytic double Michael cascade reaction: forging five stereocenters in structurally diverse hexahydroxanthones
inferred← citeshttps://doi.org/10.1039/d1np00003aopenalex-snapshot
Recent advances in total syntheses of natural products containing the benzocycloheptane motif
inferred← citeshttps://doi.org/10.1039/d3ob00126aopenalex-snapshot
Asymmetric synthesis of spirocyclic isobenzofuranones via a squaramide-catalysed sulfa-Michael desymmetrisation reaction
inferred← citeshttps://doi.org/10.1039/d4ob01560fopenalex-snapshot
H 3 PO 3 promoted reactions of thioamides with 2-substituted benzyl alcohols
inferred← citeshttps://doi.org/10.1055/a-1657-2068openalex-snapshot
Cooperative Rh(II)/Pd(0) Dual Catalysis for the Synthesis of Carbo- and Heterocyclic Compounds
inferred← citeshttps://doi.org/10.1073/pnas.1417304111openalex-snapshot
Pictet–Spengler reaction-based biosynthetic machinery in fungi
inferred← citeshttps://doi.org/10.1080/00397911.2017.1334918openalex-snapshot
Synthesis, characterization, and investigations of antimicrobial activity of 6,6-dimethyl-3-aryl-3′,4′,6,7-tetrahydro-1′H,3H-spiro[benzofuran-2,2′-naphthalene]-1′,4(5H)-dione
inferred← citeshttps://doi.org/10.1080/14786419.2010.487188openalex-snapshot
An aporphine alkaloid fromNelumbo nuciferaas an acetylcholinesterase inhibitor and the primary investigation for structure–activity correlations
inferred← citeshttps://doi.org/10.1080/14786419.2018.1443091openalex-snapshot
Biologically active oligostilbenes from the stems of Vatica mangachapoi and chemotaxonomic significance
inferred← citeshttps://doi.org/10.1096/fj.13-231613openalex-snapshot
Antitumor effects of naturally occurring oligomeric resveratrol derivatives
inferred← citeshttps://doi.org/10.1098/rsos.231510openalex-snapshot
One-pot domino syntheses of 3-alkyl-3- N -substituted aminobenzofuran-2(3 H )-ones based on alkali-promoted Michael addition and lactonization
inferred← citeshttps://doi.org/10.1111/acel.12022openalex-snapshot
Hopeahainol A attenuates memory deficits by targeting β‐amyloid in APP / PS 1 transgenic mice
inferred← citeshttps://doi.org/10.1155/jfbc/6643716openalex-snapshot
Screening and Characterization of Potential Acetylcholinesterase Inhibitors From Phyllanthus emblica L. Fruits Using Affinity Ultrafiltration Combined With Ultra‐High‐Performance Liquid Chromatography–Mass Spectrometry
inferred← citeshttps://doi.org/10.1246/bcsj.20230182openalex-snapshot
Catalyst Design with Small Organic Ion Pairs
inferred← citeshttps://doi.org/10.1515/hepo-2016-0024openalex-snapshot
Fumigant toxicities of essential oils and two monoterpenes against potato tuber moth (Phthorimaea operculellaZeller)
inferred← citeshttps://doi.org/10.2174/1570159x11311040004openalex-snapshot
Natural AChE Inhibitors from Plants and their Contribution to Alzheimer’s Disease Therapy
inferred← citeshttps://doi.org/10.2174/1570159x113116660047openalex-snapshot
Multi-Target-Directed Ligands and other Therapeutic Strategies in the Search of a Real Solution for Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3389/fpls.2022.830413openalex-snapshot
Integrated Metabolome and Transcriptome Analyses Reveal Dissimilarities in the Anthocyanin Synthesis Pathway Between Different Developmental Leaf Color Transitions in Hopea hainanensis (Dipterocarpaceae)
inferred← citeshttps://doi.org/10.3390/catal9020192openalex-snapshot
NHC-Catalyzed Organocatalytic Asymmetric Approach to 2,2-Disubstituted Benzofuran-3(2H)-ones Containing Fully Substituted Quaternary Stereogenic Center
inferred← citeshttps://doi.org/10.3390/md15080244openalex-snapshot
Strepchazolins A and B: Two New Alkaloids from a Marine Streptomyces chartreusis NA02069
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.73.140openalex-snapshot
Development of Ion-Paired Chiral Ligands for Asymmetric Transition-Metal Catalysis
inferred← citeshttps://doi.org/10.5772/27974openalex-snapshot
Construction of Drug Screening Cell Model and Application to New Compounds Interfering Production and Accumulation of Beta-Amyloid by Inhibiting Gamma-Secretase
inferred← citeshttps://doi.org/10.6023/cjoc202206008openalex-snapshot
Design, Synthesis, Fungicidal Activity and Molecular Docking Study of Novel 2-(1-Methyl-1H-pyrazol-4-yl)pyrimidine-4-carboxamides
inferred← citeshttps://doi.org/10.71267/mencom.7842openalex-snapshot
Photochemical synthesis of 3-trifluoromethyl-2,3-dihydrobenzofuran-3-ols
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