On the public citation graph

Antiviral activity of arylnaphthalene and aryldihydronaphthalene lignans

https://doi.org/10.1139/v00-059
0 signed · 77 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/ardp.19933260709openalex-snapshot
Synthesis and Biological Activity of Bromolignans and Cyclolignans
inferredcites →https://doi.org/10.1016/s0040-4020(01)93074-1openalex-snapshot
The isolation and structure of three new lignans from Justicia procumbens Linn. var. leucantha honda
inferredcites →https://doi.org/10.1016/s0040-4039(00)86892-6openalex-snapshot
A convergent mercury mediated lignan synthesis
inferredcites →https://doi.org/10.1016/s0040-4039(00)98577-0openalex-snapshot
A new route to 1-phenylnaphthalenes by cycloaddition: a simple and selective synthesis of some naphthalene lignan lactones
inferredcites →https://doi.org/10.1016/s0166-3542(98)00028-xopenalex-snapshot
The antiviral activity of the ribonucleotide reductase inhibitor BILD 1351 SE in combination with acyclovir against HSV type-1 in cell culture
inferredcites →https://doi.org/10.1017/cbo9780511983665openalex-snapshot
Lignans
inferredcites →https://doi.org/10.1021/jm9807048openalex-snapshot
1-Arylnaphthalene Lignan: A Novel Scaffold for Type 5 Phosphodiesterase Inhibitor
inferredcites →https://doi.org/10.1021/jo00119a041openalex-snapshot
Efficient Syntheses of 1-Arylnaphthalene Lignan Lactones and Related Compounds from Cyanohydrins
inferredcites →https://doi.org/10.1021/jo960295sopenalex-snapshot
Tandem Pummerer−Diels−Alder Reaction Sequence. A Novel Cascade Process for the Preparation of 1-Arylnaphthalene Lignans
inferredcites →https://doi.org/10.1021/np50062a024openalex-snapshot
Improved Methods of Synthesis of Lignan Arylnaphthalene Lactones via Arylpropargyl Arylpropiolate Esters
inferredcites →https://doi.org/10.1021/np980136zopenalex-snapshot
Antiviral Activity of Lignans
inferredcites →https://doi.org/10.1039/np9931000001openalex-snapshot
Lignans neolignans, and related compounds
inferredcites →https://doi.org/10.1039/np9951200183openalex-snapshot
Lignans, neolignans, and related compounds
inferredcites →https://doi.org/10.1039/np9971400043openalex-snapshot
Lignans, neolignans and related compounds
inferredcites →https://doi.org/10.1039/p19950000235openalex-snapshot
Facile construction of the 1-phenylnaphthyl skeleton via an ester-mediated nucleophilic aromatic substitution reaction. Applications to the synthesis of phenylnaphthalide lignans
inferredcites →https://doi.org/10.1139/v90-309openalex-snapshot
Asymmetric synthesis of podophyllotoxin analogs

What points at this work

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

inferred← citeshttps://doi.org/10.3897/pharmacia.71.e117690zenodo-depositor-declared
Arylnaphthalene lignans with a focus Linum species: a review on phytochemical, biotechnological and pharmacological potential
inferred← citeshttps://doi.org/10.1002/9781118682784.ch11openalex-snapshot
Biological Properties of Lignans
inferred← citeshttps://doi.org/10.1002/adsc.200600587openalex-snapshot
Synthesis of Biaryls via Palladium‐Catalyzed [2+2+2] Cocyclization of Arynes and Diynes: Application to the Synthesis of Arylnaphthalene Lignans
inferred← citeshttps://doi.org/10.1002/adsc.201000269openalex-snapshot
Iron and Copper Salts in the Synthesis of Benzo[ b ]furans
inferred← citeshttps://doi.org/10.1002/ange.200453809openalex-snapshot
Arylnaphthalene Lignans through Pd‐Catalyzed [2+2+2] Cocyclization of Arynes and Diynes: Total Synthesis of Taiwanins C and E
inferred← citeshttps://doi.org/10.1002/anie.200453809openalex-snapshot
Arylnaphthalene Lignans through Pd‐Catalyzed [2+2+2] Cocyclization of Arynes and Diynes: Total Synthesis of Taiwanins C and E
inferred← citeshttps://doi.org/10.1002/chem.201501978openalex-snapshot
Synthesis, Photophysics, and Self‐Assembly of Furan‐Embedded Heteroarenes
inferred← citeshttps://doi.org/10.1002/chin.200042211openalex-snapshot
ChemInform Abstract: Antiviral Activity of Arylnaphthalene and Aryldihydronaphthalene Lignans.
inferred← citeshttps://doi.org/10.1002/mrc.2065openalex-snapshot
Complete assignments of 1H and 13C NMR spectral data for arylnaphthalene lignan lactones
inferred← citeshttps://doi.org/10.1007/978-3-7091-6227-9_1openalex-snapshot
Biaryls in Nature: A Multi-Facetted Class of Stereochemically, Biosynthetically, and Pharmacologically Intriguing Secondary Metabolites
inferred← citeshttps://doi.org/10.1007/s11101-020-09735-zopenalex-snapshot
Arylnaphthalene lactones: structures and pharmacological potentials
inferred← citeshttps://doi.org/10.1016/j.bmc.2004.05.036openalex-snapshot
Preparation and anti-HIV activities of retrojusticidin B analogs and azalignans
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.07.017openalex-snapshot
Methyltrioxorhenium catalysed synthesis of highly oxidised aryltetralin lignans with anti-topoisomerase II and apoptogenic activities
inferred← citeshttps://doi.org/10.1016/j.bmc.2009.12.038openalex-snapshot
Synthesis and the biological evaluation of arylnaphthalene lignans as anti-hepatitis B virus agents
inferred← citeshttps://doi.org/10.1016/j.fitote.2014.01.025openalex-snapshot
Cytotoxic activity of lignans from Justicia procumbens
inferred← citeshttps://doi.org/10.1016/j.phymed.2023.155197openalex-snapshot
Exploring the antiviral potential of justicidin B and four glycosylated lignans from Phyllanthus brasiliensis against Zika virus: A promising pharmacological approach
inferred← citeshttps://doi.org/10.1016/j.phytochem.2009.07.029openalex-snapshot
Antihyperglycemic activity of phenylpropanoyl esters of catechol glycoside and its dimers from Dodecadenia grandiflora
inferred← citeshttps://doi.org/10.1016/j.phytochem.2012.07.004openalex-snapshot
Lignans in seeds of Linum species
inferred← citeshttps://doi.org/10.1016/j.tet.2005.10.054openalex-snapshot
Efficient synthesis of 1,4-dihydronaphthalenelignans from 5-methylene-4-substituted-2(5H)-furanones and a concise synthesis of solafuranone
inferred← citeshttps://doi.org/10.1016/j.tet.2015.03.023openalex-snapshot
Synthesis of arylnaphthalene lignan lactone using benzoin condensation, intramolecular thermal cyclization and Suzuki coupling
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132214openalex-snapshot
Triflic acid catalysed regioselective synthesis of substituted naphthalenes by benzannulation of carbonyls with alkynes
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132573openalex-snapshot
Applications of Claisen condensations in total synthesis of natural products. An old reaction, a new perspective
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.01.042openalex-snapshot
Microwave assisted synthesis and cytotoxic activity evaluations of new benzimidazole derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.156149openalex-snapshot
Indium chloride catalysed annulation of arylmethyl carbonyls & arylalkynes for the synthesis of naphthalene derivatives
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)00616-6openalex-snapshot
A new benzannulation reaction and its application in the multiple parallel synthesis of arylnaphthalene lignans
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)01436-8openalex-snapshot
Total syntheses of justicidin B and retrojusticidin B using a tandem Horner–Emmons–Claisen condensation sequence
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00180openalex-snapshot
A Removable Acyl Group Promoted the Intramolecular Dehydro-Diels–Alder Reaction of Styrene-Ynes: Highly Chemoselective Synthesis of Aryldihydronaphthalene Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.5c03010openalex-snapshot
Cu(II)-Catalyzed Benzannulation of Triynols to Synthesize β-Naphthyl Ketones Using Methanol as a Traceless Protective Agent
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01278openalex-snapshot
Bi(OTf)3-Mediated Intramolecular Olefinic Cyclization: Synthesis of Substituted Aryl-Dihydronaphthalenes and Indenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02286openalex-snapshot
Photoredox Generated Carbonyl Ylides Enable a Modular Approach to Aryltetralin, Dihydronaphthalene, and Arylnaphthalene Lignans
inferred← citeshttps://doi.org/10.1021/acssuschemeng.0c05156openalex-snapshot
Brønsted Acid Ionic Liquid-Catalyzed Ring Opening of 3,3-Disubstituted Oxetanes in Water: Efficient Access to Furans and Benzofurans
inferred← citeshttps://doi.org/10.1021/jm200737sopenalex-snapshot
Polyalkoxybenzenes from Plants. 5. Parsley Seed Extract in Synthesis of Azapodophyllotoxins Featuring Strong Tubulin Destabilizing Activity in the Sea Urchin Embryo and Cell Culture Assays
inferred← citeshttps://doi.org/10.1021/jo0161025openalex-snapshot
Acid-Catalyzed Cyclization of 2,3-Dibenzylidenesuccinates: Synthesis of Lignans (±)-Cagayanin and (±)-Galbulin
inferred← citeshttps://doi.org/10.1021/jo0497454openalex-snapshot
A Short Asymmetric Synthesis of (+)-Lyoniresinol Dimethyl Ether
inferred← citeshttps://doi.org/10.1021/jo051299copenalex-snapshot
Synthesis of 2,3-Disubstituted Benzo[b]furans by the Palladium-Catalyzed Coupling ofo-Iodoanisoles and Terminal Alkynes, Followed by Electrophilic Cyclization
inferred← citeshttps://doi.org/10.1021/jo201841yopenalex-snapshot
Regioselective Preparation of Benzo[b]furans from Phenols and α-Bromoketones
inferred← citeshttps://doi.org/10.1021/jo201918dopenalex-snapshot
Synthesis of Arylnaphthalene Lignan Scaffold by Gold-Catalyzed Intramolecular Sequential Electrophilic Addition and Benzannulation
inferred← citeshttps://doi.org/10.1021/jo801213mopenalex-snapshot
Silver-Catalyzed One-Pot Synthesis of Arylnaphthalene Lactones
inferred← citeshttps://doi.org/10.1021/jo9016309openalex-snapshot
PdCl2-Promoted Electrophilic Annulation of 2-Alkynylphenol Derivatives with Disulfides or Diselenides in the Presence of Iodine
inferred← citeshttps://doi.org/10.1021/np900667hopenalex-snapshot
Silver-Catalyzed One-Pot Synthesis of Arylnaphthalene Lactone Natural Products
inferred← citeshttps://doi.org/10.1021/ol501853yopenalex-snapshot
Intramolecular Dehydro-Diels–Alder Reaction Affords Selective Entry to Arylnaphthalene or Aryldihydronaphthalene Lignans
inferred← citeshttps://doi.org/10.1023/b:phyt.0000045497.90158.d2openalex-snapshot
Lignans and neolignans as lead compounds
inferred← citeshttps://doi.org/10.1039/b913685aopenalex-snapshot
Advances in the methodology of a multicomponent synthesis of arylnaphthalene lactones
inferred← citeshttps://doi.org/10.1039/c3sc51489gopenalex-snapshot
Benzofuran synthesis via copper-mediated oxidative annulation of phenols and unactivated internal alkynes
inferred← citeshttps://doi.org/10.1039/c7ra13754kopenalex-snapshot
Arylnaphthalene lactone analogues: synthesis and development as excellent biological candidates for future drug discovery
inferred← citeshttps://doi.org/10.1039/d0ra01907kopenalex-snapshot
Synthesis of 3-selanylbenzo[ b ]furans promoted by SelectFluor®
inferred← citeshttps://doi.org/10.1039/d4ra06517dopenalex-snapshot
Chemical synthesis and application of aryldihydronaphthalene derivatives
inferred← citeshttps://doi.org/10.1039/d5tc02120kopenalex-snapshot
Recent advances in the O-doped polycyclic aromatic hydrocarbons
inferred← citeshttps://doi.org/10.1080/00397911.2020.1794656openalex-snapshot
A non-lithiation route towards facile synthesis of bioactive 4, 9-dimethoxynaphthalide
inferred← citeshttps://doi.org/10.1139/v04-143openalex-snapshot
The complex photochemistry of 2,3-dibenzylidenesuccinates
inferred← citeshttps://doi.org/10.1186/s12870-025-07476-9openalex-snapshot
Integrative metabolomic and transcriptomic analyses reveal key mechanisms of lignan biosynthesis during sesame (Sesamum indicum L.) seed development
inferred← citeshttps://doi.org/10.1246/cl.141061openalex-snapshot
First Total Synthesis of (+)-Podophyllic Aldehydes
inferred← citeshttps://doi.org/10.1246/cl.2010.194openalex-snapshot
Lewis Acid-mediated Highly Regioselective Ring-expansion of Methyl 2-Phenyl-1-(arylhydroxymethyl)cyclopropanecarboxylates
inferred← citeshttps://doi.org/10.1248/cpb.53.930openalex-snapshot
First Total Synthesis of Justicidone, a p-Quinone-Lignan Derivative from Justicia hyssopifolia
inferred← citeshttps://doi.org/10.1590/s0102-695x2012005000110openalex-snapshot
Antiviral activity of fractions from leaves of Piper regnelli var. pallescens
inferred← citeshttps://doi.org/10.3184/174751915x14425727961796openalex-snapshot
Total Synthesis of Cannabisin B
inferred← citeshttps://doi.org/10.3389/fchem.2020.00628openalex-snapshot
Transition Metal-Mediated Annulation Approaches for Synthesis of Arylnaphthalene Lignan Lactones
inferred← citeshttps://doi.org/10.3390/cryst11080857openalex-snapshot
4-Phenylnaphtho[2,3-c]furan-1(3H)-one, 9-Phenylnaphtho[2,3-c]furan-1(3H)-one and 3a,4-Dihydro-9-phenylnaphtho[2,3-c]furan-1(3H)-one Crystal Structures
inferred← citeshttps://doi.org/10.3390/molecules200916566openalex-snapshot
Benzofuranyl Esters: Synthesis, Crystal Structure Determination, Antimicrobial and Antioxidant Activities
inferred← citeshttps://doi.org/10.3390/molecules21070820openalex-snapshot
Justicidin B: A Promising Bioactive Lignan
inferred← citeshttps://doi.org/10.3390/molecules23123385openalex-snapshot
Advances in the Synthesis of Lignan Natural Products
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.