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Dibenzofurans and derivatives from lichens and ascomycetes

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What this work says

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

inferredcites →https://doi.org/10.1001/archderm.92.2.142openalex-snapshot

Allergy to lichens. Allergic contact dermatitis from usnic acid produced by lichenized fungi

inferredcites →https://doi.org/10.1002/ajoc.201300081openalex-snapshot

Identification of Boletopsin 11 and 12, Antibiotics from the Traditionally Used Fungus Boletopsis sp.

inferredcites →https://doi.org/10.1002/cbdv.200490050openalex-snapshot

DPPH Radical Scavenging Activity of Ten Natural p‐Terphenyl Derivatives Obtained from Three Edible Mushrooms Indigenous to China

inferredcites →https://doi.org/10.1002/cbdv.201400146openalex-snapshot

Identification and Biological Evaluation of Secondary Metabolites from the Endolichenic Fungus Aspergillus versicolor

inferredcites →https://doi.org/10.1002/ejoc.200400870openalex-snapshot

Fulicineroside, an Unusual Glycosidic Dibenzofuran Metabolite from the Slime Mold Fuligo cinerea (Schwein.) Morgan

inferredcites →https://doi.org/10.1002/ejoc.201600252openalex-snapshot

Cyaneodimycin, a Bioactive Compound Isolated from the Culture of Streptomyces cyaneofuscatus Associated with Lichina confinis

inferredcites →https://doi.org/10.1002/ptr.4739openalex-snapshot

Cytotoxic Activity and Antioxidant Capacity of Purified Lichen Metabolites: An In Vitro Study

inferredcites →https://doi.org/10.1007/978-3-642-45410-3openalex-snapshot

Chemistry of Plant Natural Products

inferredcites →https://doi.org/10.1007/978-3-642-85243-5openalex-snapshot

Identification of Lichen Substances

inferredcites →https://doi.org/10.1007/s00114-002-0305-3openalex-snapshot

A review on usnic acid, an interesting natural compound

inferredcites →https://doi.org/10.1007/s00894-005-0047-1openalex-snapshot

Bioactive principles in the bark of Pilidiostigma tropicum

inferredcites →https://doi.org/10.1007/s10096-012-1706-7openalex-snapshot

Membrane-damaging potential of natural L-(−)-usnic acid in Staphylococcus aureus

inferredcites →https://doi.org/10.1007/s10482-014-0324-zopenalex-snapshot

Usnic acid, a lichen secondary metabolite inhibits Group A Streptococcus biofilms

inferredcites →https://doi.org/10.1007/s10600-012-0097-4openalex-snapshot

Porric acid D from marine-derived fungus Alternaria sp. isolated from Bohai Sea

inferredcites →https://doi.org/10.1007/s11557-006-0117-5openalex-snapshot

Chemical variation in the lichen genus Letrouitia (Ascomycota, Letrouitiaceae)

inferredcites →https://doi.org/10.1007/s11814-009-0044-7openalex-snapshot

Synthesis of nanometer sized Bi2WO6s by a hydrothermal method and their conductivities

inferredcites →https://doi.org/10.1016/0031-9422(92)83434-zopenalex-snapshot

Usnic acid amide, a phytotoxin and antifungal agent from Cercosporidium henningsii

inferredcites →https://doi.org/10.1016/0031-9422(93)80057-yopenalex-snapshot

Hypostrepsilic acid, a new dibenzofuran from the culturei lichen mycobiont of Evernia esorediosa

inferredcites →https://doi.org/10.1016/0031-9422(93)85097-bopenalex-snapshot

Toxicity and antifeedant activity of lichen compounds against the polyphagous herbivorous insect Spodoptera littoralis

inferredcites →https://doi.org/10.1016/0031-9422(94)00731-8openalex-snapshot

Phenols and a dioxotetrahydrodibenzofuran from seeds of Iris pallasii

inferredcites →https://doi.org/10.1016/0040-4039(81)80095-0openalex-snapshot

The absolute configurations of (+)-usnic and (+)-isousnic acid. X-ray analyses of the (−)-α-phenylethylamine derivative of (+)-usnic acid and of (−)-pseudoplacodiolic acid, a new dibenzofuran, from the lichen .

inferredcites →https://doi.org/10.1016/0305-1978(83)90003-0openalex-snapshot

Genetic and environmental effects of growth and production of secondary compounds in Cladonia cristatella

inferredcites →https://doi.org/10.1016/j.bcp.2003.09.032openalex-snapshot

Usnic acid-induced necrosis of cultured mouse hepatocytes: inhibition of mitochondrial function and oxidative stress

inferredcites →https://doi.org/10.1016/j.bmc.2008.05.069openalex-snapshot

Synthesis and cytotoxic activities of usnic acid derivatives

inferredcites →https://doi.org/10.1016/j.bmc.2013.05.022openalex-snapshot

Novel chlorinated dibenzofurans isolated from the cellular slime mold, Polysphondylium filamentosum, and their biological activities

inferredcites →https://doi.org/10.1016/j.bmc.2014.02.058openalex-snapshot

Structural elucidation and synthesis of vialinin C, a new inhibitor of TNF-α production

inferredcites →https://doi.org/10.1016/j.bmcl.2006.07.068openalex-snapshot

Vialinin B, a novel potent inhibitor of TNF-α production, isolated from an edible mushroom, Thelephora vialis

inferredcites →https://doi.org/10.1016/j.envexpbot.2004.10.011openalex-snapshot

Lichen chemistry and selective grazing by the coleopteran Lasioderma serricorne

inferredcites →https://doi.org/10.1016/j.fitote.2004.04.002openalex-snapshot

Intermediate reactive oxygen and nitrogen from macrophages induced by Brazilian lichens

inferredcites →https://doi.org/10.1016/j.fitote.2014.01.003openalex-snapshot

Antiplasmodial and Cytotoxic Dibenzofurans from Preussia sp. harboured in Enantia chlorantha Oliv

inferredcites →https://doi.org/10.1016/j.funbio.2015.10.009openalex-snapshot

Putative identification of the usnic acid biosynthetic gene cluster by de novo whole-genome sequencing of a lichen-forming fungus

inferredcites →https://doi.org/10.1016/j.jep.2005.06.043openalex-snapshot

Gastroprotective and antioxidant effects of usnic acid on indomethacin-induced gastric ulcer in rats

inferredcites →https://doi.org/10.1016/j.jhep.2004.06.028openalex-snapshot

Severe hepatotoxicity associated with the use of weight loss diet supplements containing ma huang or usnic acid

inferredcites →https://doi.org/10.1016/j.jhep.2004.07.006openalex-snapshot

Acute hepatitis of cholestatic type possibly associated with the use of glucomannan (amorphophalus konjac)

inferredcites →https://doi.org/10.1016/j.micres.2005.08.006openalex-snapshot

Experimental studies on the growth and usnic acid production in “lichen” Usnea ghattensis in vitro

inferredcites →https://doi.org/10.1016/j.phymed.2012.11.003openalex-snapshot

Achyrofuran is an antibacterial agent capable of killing methicillin-resistant vancomycin-intermediate Staphylococcus aureus in the nanomolar range

inferredcites →https://doi.org/10.1016/j.phytochem.2004.12.031openalex-snapshot

Monomeric and dimeric dibenzofurans from cultured mycobionts of Lecanora iseana

inferredcites →https://doi.org/10.1016/j.phytochem.2007.10.031openalex-snapshot

Purification, identification and activity of phomodione, a furandione from an endophytic Phoma species

inferredcites →https://doi.org/10.1016/j.phytochem.2008.12.016openalex-snapshot

Dibenzofuran and pyranone metabolites from Hypericum revolutum ssp. revolutum and Hypericum choisianum

inferredcites →https://doi.org/10.1016/j.phytol.2012.10.009openalex-snapshot

Usnic acid derivatives from Leprocaulon microscopicum

inferredcites →https://doi.org/10.1016/j.tet.2010.04.111openalex-snapshot

Three new sorbicillin trimers, trisorbicillinones B, C, and D, from a deep ocean sediment derived fungus, Phialocephala sp. FL30r

inferredcites →https://doi.org/10.1016/j.tetlet.2006.01.012openalex-snapshot

Kehokorins A–C, novel cytotoxic dibenzofurans isolated from the myxomycete Trichia favoginea var. persimilis

inferredcites →https://doi.org/10.1016/s0031-9422(00)80419-7openalex-snapshot

Crystal structure of (−)-placodiolic acid, a dibenzofuran derivative from the lichen Rhizoplaca chrysoleuca

inferredcites →https://doi.org/10.1016/s0031-9422(01)00394-6openalex-snapshot

Dibenzofurans from the cultured lichen mycobionts of Lecanora cinereocarnea

inferredcites →https://doi.org/10.1016/s0031-9422(02)00383-7openalex-snapshot

Usnic acid

inferredcites →https://doi.org/10.1016/s0031-9422(97)00501-3openalex-snapshot

Hypostrepsilalic acid from a cultured lichen mycobiont of Stereocaulon Japonicum

inferredcites →https://doi.org/10.1016/s0040-4020(01)93847-5openalex-snapshot

Flechteninhaltsstoffe—XCIII

inferredcites →https://doi.org/10.1016/s0040-4039(00)01879-7openalex-snapshot

Novel aromatic substances, dictyomedin A and B, from Dictyostelium cellular slime molds and their inhibitory effects on Dictyostelium development

inferredcites →https://doi.org/10.1021/cc050122topenalex-snapshot

Solid-Phase Synthesis of Polyfunctionalized Natural Products: Application to Usnic Acid, a Bioactive Lichen Compound

inferredcites →https://doi.org/10.1021/jf1049613openalex-snapshot

Isolation, Characterization and Antifungal Activity of Major Constituents of the Himalayan Lichen Parmelia reticulata Tayl.†

inferredcites →https://doi.org/10.1021/jm00197a019openalex-snapshot

Usnic acid derivatives as potential antineoplastic agents

inferredcites →https://doi.org/10.1021/jo00003a002openalex-snapshot

The structure and biological activity of cercosporamide from Cercosporidium henningsii

inferredcites →https://doi.org/10.1021/np049843kopenalex-snapshot

Karnatakafurans A and B: Two Dibenzofurans Isolated from the Fungus Aspergillus k arnatakaensis

inferredcites →https://doi.org/10.1021/np070464bopenalex-snapshot

Usimines A−C, Bioactive Usnic Acid Derivatives from the Antarctic Lichen Stereocaulon alpinum

inferredcites →https://doi.org/10.1021/np100113eopenalex-snapshot

KDR Kinase Inhibitor Isolated from the Mushroom Boletopsis leucomelas

inferredcites →https://doi.org/10.1021/np300433ropenalex-snapshot

Biologically Active Dibenzofurans from Pilidiostigma glabrum, an Endemic Australian Myrtaceae

inferredcites →https://doi.org/10.1021/np300566yopenalex-snapshot

Nerve Growth Factor-Potentiating Benzofuran Derivatives from the Medicinal Fungus Phellinus ribis

inferredcites →https://doi.org/10.1021/np50109a009openalex-snapshot

Alectosarmentin, a New Antimicrobial Dibenzofuranoid Lactol from the Lichen, Alectoria sarmentosa

inferredcites →https://doi.org/10.1055/s-0029-1185329openalex-snapshot

Antiproliferative Effects on Tumour Cells and Promotion of Keratinocyte Wound Healing by Different Lichen Compounds

inferredcites →https://doi.org/10.1055/s-0034-1382827openalex-snapshot

Uncommon Chlorinated Xanthone and Other Antibacterial Compounds from the Lichen Cladonia incrassata

inferredcites →https://doi.org/10.1055/s-2004-827240openalex-snapshot

Cytotoxic Activity of Compounds from the Lichen:Cladonia convoluta

inferredcites →https://doi.org/10.1055/s-2006-958027openalex-snapshot

Usnic Acid and Diffractaic Acid as Analgesic and Antipyretic Components ofUsnea diffracta

inferredcites →https://doi.org/10.1071/ch9811501openalex-snapshot

Condidymic acid, a new dibenzofuran from the lichen Cladonia squamosula

inferredcites →https://doi.org/10.1071/ch9861759openalex-snapshot

Isodidymic Acid, a New Dibenzofuran From the Lichen .Cladonia didyma

inferredcites →https://doi.org/10.1071/ch9920785openalex-snapshot

A Synthesis of the Lichen Dibenzofuran Pannaric Acid 2-Methyl Ester and Its Isomer 3-O-Methylpannaric Acid

inferredcites →https://doi.org/10.1071/ch9930407openalex-snapshot

3-O-Demethylschizopeltic Acid, a New Dibenzofuran From the Lichen Roccella hypomecha

inferredcites →https://doi.org/10.1071/ch9940703openalex-snapshot

The Structure and Synthesis of 4-Oxypannaric Acid 2-Methyl Ester, a Dibenzofuran From the Lichen Leproloma diffusum

inferredcites →https://doi.org/10.1071/ch9941335openalex-snapshot

New Dibenzofurans and Depsides From the Lichen Bunodophoron patagonicum

inferredcites →https://doi.org/10.1080/00275514.1980.12021158openalex-snapshot

Artificial Reestablishment of Lichens. II. Secondary Products of Resynthesized Cladonia Cristatella and Lecanora Chrysoleuca

inferredcites →https://doi.org/10.1080/10286020.2011.622720openalex-snapshot

A new depsidone and antibacterial activities of compounds fromUsnea undulataStirton

inferredcites →https://doi.org/10.1111/1574-6968.12409openalex-snapshot

Antibacterial activity of lichen secondary metabolite usnic acid is primarily caused by inhibition of RNA and DNA synthesis

inferredcites →https://doi.org/10.1111/j.0105-1873.2005.00495.xopenalex-snapshot

Occupational allergic contact dermatitis from lichens in present‐day Finland

inferredcites →https://doi.org/10.1127/herzogia/13/1998/145openalex-snapshot

The structure of isoplacodiolic acid and isopseudoplacodiolic acid, two new dibenzofuran derivatives from the lichen genus Haematomma

inferredcites →https://doi.org/10.1128/aac.48.11.4360-4365.2004openalex-snapshot

Usnic Acid, a Natural Antimicrobial Agent Able To Inhibit Bacterial Biofilm Formation on Polymer Surfaces

inferredcites →https://doi.org/10.1139/b86-212openalex-snapshot

Allelopathic effects of Cladonia cristatella on ectomycorrhizal fungi common to bituminous strip-mine spoils

inferredcites →https://doi.org/10.1248/cpb.40.3194openalex-snapshot

5-Lipoxygenase Inhibitors Isolated from the Mushroom Boletopsis leucomelas (Pers.) Fayod.

inferredcites →https://doi.org/10.1248/cpb.44.441openalex-snapshot

A Novel Dibenzofuran and Two New Xanthones from Calophyllum panciflorum.

inferredcites →https://doi.org/10.1248/cpb.56.439openalex-snapshot

Fortuneanosides G-L, Dibenzofuran Glycosides from the Fruit of Pyracantha fortuneana

inferredcites →https://doi.org/10.1248/cpb.56.89openalex-snapshot

Novel Abietane Diterpenoids and Aromatic Compounds from Cladonia rangiferina and Their Antimicrobial Activity against Antibiotics Resistant Bacteria

inferredcites →https://doi.org/10.1248/cpb1953.5.539openalex-snapshot

Antibacterial Effect of Lichen Substances and Related Compounds. V. Dibenzofuran Derivatives. (3).

inferredcites →https://doi.org/10.1515/bot.2010.064openalex-snapshot

Dibenzofurans from the marine sponge-derived ascomycete Super1F1-09

inferredcites →https://doi.org/10.1515/znb-1991-0716openalex-snapshot

Notizen: 3-O-Methylpannaric Acid from the Lichen Roccella capensis

inferredcites →https://doi.org/10.1515/znb-1994-0922openalex-snapshot

Haemophaein, ein Dibenzofuran aus der Flechte Phyllopsora haemophaea / Haemophaein, a Dibenzofuran from the Lichen Phyllopsora haemophaea

inferredcites →https://doi.org/10.1515/znc-1981-9-1034openalex-snapshot

Pannarsäure und Porphyrilsäuremethylester — Sekundärstoffe der Flechtengattung Psoroma / Pannaric Acid and Prophyrilic Acid Methyl Ester Lichen Substances in the Genus Psorma

inferredcites →https://doi.org/10.1515/znc-1986-11-1227openalex-snapshot

Vorarbeiten zu einer Monographie der Flechtenfamilie Roccellaceae Chev. VII. Inhaltsstoffe und Verwandtschaftsbeziehungen der Gattungen Combea de Not. und Schizopelte T. M. Fries / Preliminary Studies towards a Monograph of the Lichen Family Roccellaceae Chev. VII. Secondary Products and…

inferredcites →https://doi.org/10.1515/znc-1992-7-802openalex-snapshot

Chemical Constituents of the Lichen Stereocaulon azoreum

inferredcites →https://doi.org/10.1515/znc-2004-5-612openalex-snapshot

Antioxidant Properties of Natural p-Terphenyl Derivatives from the Mushroom Thelephora ganbajun

inferredcites →https://doi.org/10.1515/znc-2010-1-206openalex-snapshot

Antibacterial Activities of Ramalin, Usnic Acid and its Three Derivatives Isolated from the Antarctic Lichen Ramalina terebrata

inferredcites →https://doi.org/10.2307/3241602openalex-snapshot

Chemical and Botanical Guide to Lichen Products

inferredcites →https://doi.org/10.2307/3759422openalex-snapshot

Artificial Reestablishment of Lichens. II. Secondary Products of Resynthesized Cladonia cristatella and Lecanora chrysoleuca

inferredcites →https://doi.org/10.3109/13880209.2011.633089openalex-snapshot

Biopharmaceutical potential of lichens

inferredcites →https://doi.org/10.3109/13880209.2012.654396openalex-snapshot

Antioxidative and cardiovascular-protective activities of metabolite usnic acid and psoromic acid produced by lichen species Usnea complanata under submerged fermentation

inferredcites →https://doi.org/10.3390/molecules190914496openalex-snapshot

Antioxidant Activity and Mechanisms of Action of Natural Compounds Isolated from Lichens: A Systematic Review

inferredcites →https://doi.org/10.3762/bjoc.8.68openalex-snapshot

Phytoalexins of the Pyrinae: Biphenyls and dibenzofurans

inferredcites →https://doi.org/10.3891/acta.chem.scand.13-1855openalex-snapshot

Studies on the Chemistry of Lichens. XIII. The Structure of Pannaric Acid.

inferredcites →https://doi.org/10.3906/kim-1008-847openalex-snapshot

Antioxidant phenolics from Lobaria pulmonaria (L.) Hoffm. and Usnea longissima Ach. lichen species

inferredcites →https://doi.org/10.4314/star.v2i4.14openalex-snapshot

Anticaries Activity of Usnea pictoides G. Awasthi -A macrolichen from Western Ghats of Karnataka, India

inferredcites →https://doi.org/10.5012/bkcs.2009.30.1.261openalex-snapshot

Identification of New Dibenzofurans from Distylium racemosum

inferredcites →https://doi.org/10.5897/ajb11.3551openalex-snapshot

Antimycobacterial activity of Usnea steineri and its major constituent (+)-usnic acid

inferredcites →https://doi.org/10.5897/jmpr10.873openalex-snapshot

Anti-inflammatory effects and mechanisms of usnic acid, a compound firstly isolated from lichen Parmelia saxatilis

inferredcites →https://doi.org/10.70675/a962d0f8z0f7bz4b19z872dz3e2989660037openalex-snapshot

Etude de quatre lichens marins, maritime ou terrestre et des bactéries associées : Evaluation de la diversité bactérienne et recherche de métabolites d’intérêt

inferredcites →https://doi.org/10.7164/antibiotics.53.959openalex-snapshot

Structure Determination and Total Synthesis of a Novel Antibacterial Substance, AB0022A, Produced by a Cellular Slime Mold.

inferredcites →https://doi.org/10.7164/antibiotics.57.465openalex-snapshot

A New Antimicrobial Dibenzofuran Sch 725421 from an Unidentified Fungus

inferredcites →https://doi.org/10.7883/yoken1948.2.22openalex-snapshot

ANTIBACTERIAL EFFECTS OF LICHEN SUBSTANCES II. STUDIES ON DIDYMIC ACID AND RELATED COMPOUNDS

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.2020.112535zenodo-depositor-declared

Lichen-associated bacteria transform antibacterial usnic acid to products of lower antibiotic activity

inferred← citeshttps://doi.org/10.1002/adsc.202300879openalex-snapshot

One‐Pot Synthesis of Bis‐sulfonyl Dibenzofurans via K2CO3‐Mediated Benzannulation of α‐Sulfonyl o‐Hydroxyacetophenones with 1,4‐Dichloro‐2‐butyne

inferred← citeshttps://doi.org/10.1002/ange.202103415openalex-snapshot

Enantioselective Synthesis of Axially Chiral Benzothiophene/Benzofuran‐Fused Biaryls by N‐Heterocyclic Carbene Catalyzed Arene Formation

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Enantioselective Synthesis of Axially Chiral Benzothiophene/Benzofuran‐Fused Biaryls by N‐Heterocyclic Carbene Catalyzed Arene Formation

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An acetatopalladium(II) complex with 1‐benzyl‐N‐(3,5‐di‐tert‐butylsalicylidene)piperidin‐4‐amine: Synthesis, structure and catalytic applications in Suzuki–Miyaura coupling of arylboronic acids with hydroxyaryl halides

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Molecular Engineering of Tetracyclic 2,3‐Dihydro‐1H‐benzo[2,3]‐benzofuro[4,5‐e][1,3]oxazine Derivatives: Evaluation for Potential Anticancer Agents

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UHPLC‐HRMS/MS Based Profiling of Algerian Lichens and Their Antimicrobial Activities

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Small Molecular Dibenzochalcogenophenes as Potent Organic Emitters

inferred← citeshttps://doi.org/10.1002/ejoc.201600252openalex-snapshot

Cyaneodimycin, a Bioactive Compound Isolated from the Culture of Streptomyces cyaneofuscatus Associated with Lichina confinis

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Naturally Occurring Organohalogen Compounds—A Comprehensive Review

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Metabolomic Analysis of the Lichen Everniopsis trulla Using Ultra High Performance Liquid Chromatography-Quadrupole-Orbitrap Mass Spectrometry (UHPLC-Q-OT-MS)

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Photochemical synthesis of novel naphtho[1,2-b]benzofuran derivatives from 2,3-disubstituted benzofurans

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Dibenzofuran Based Donor-Pi-Acceptor Molecules: Effect of Azo and Aminomethylene Linkages on Photophysical and NLO Properties

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Have lichenized fungi delivered promising anticancer small molecules?

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The application of carbon isotope compositions of fluorene and its methylated homologues in the sources and depositional environments of sedimentary organic matter

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Aromatic Compounds from Malus rockii and Their Lipid-Lowering Activities

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Five-Membered Ring Systems

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The Literature of Heterocyclic Chemistry, Part XVI, 2016

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Dibenzofurans from nature: Biosynthesis, structural diversity, sources, and bioactivities

inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.109971openalex-snapshot

Antifungal effects of dibenzofuran derivatives against multi-azole resistant Candida albicans

inferred← citeshttps://doi.org/10.1016/j.biotechadv.2022.108072openalex-snapshot

Recent advances in research for potential utilization of unexplored lichen metabolites

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Chemistry and pharmacological aspects of furanoid cannabinoids and related compounds: Is furanoid cannabinoids open a new dimension towards the non-psychoactive cannabinoids?

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A new acetophenone glycoside from the flower buds of Syzygium aromaticum (cloves)

inferred← citeshttps://doi.org/10.1016/j.fitote.2017.07.011openalex-snapshot

Antibacterial activities of natural lichen compounds against Streptococcus gordonii and Porphyromonas gingivalis

inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107333openalex-snapshot

New dibenzofurans from Phellinus ribis and their anti-inflammatory activity

inferred← citeshttps://doi.org/10.1016/j.ijantimicag.2023.106876openalex-snapshot

The usnic acid derivative peziculone targets cell walls of Gram-positive bacteria revealed by high-throughput CRISPRi-seq analysis

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Palladium-catalyzed diastereoselective synthesis of 2,2,3-trisubstituted dihydrobenzofurans via intramolecular trapping of O-ylides with activated alkenes

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Maslinic acid ameliorates NMDA receptor blockade-induced schizophrenia-like behaviors in mice

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Distribution, occurrence and identification of dibenzofuran, benzo[b]naphthofurans and their alkyl derivatives in Gippsland Basin source rocks

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Geochemical implications of the carbon isotope compositions of individual polycyclic aromatic compounds in coals from the Junggar and Ordos basins, NW China

inferred← citeshttps://doi.org/10.1016/s2707-3688(23)00049-3openalex-snapshot

Macrocyclic polyketides from microorganisms: structural diversities and bioactivities

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00831openalex-snapshot

Dibenzofurans and Pseudodepsidones from the Lichen Stereocaulon paschale Collected in Northern Quebec

inferred← citeshttps://doi.org/10.1021/acs.joc.0c00924openalex-snapshot

Switching the Mallory Reaction to Synthesis of Naphthalenes, Benzannulated Heterocycles, and Their Derivatives

inferred← citeshttps://doi.org/10.1021/acs.joc.8b00792openalex-snapshot

Total Synthesis of Boletopsin 11 Enabled by Directed ortho-C(sp2)–H Arylation

inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03472openalex-snapshot

Synthesis of Annulated Benzofuran Derivatives from α-(Iodophenyl)-β-oxoesters

inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02234openalex-snapshot

Divergent Three-Component Assembly of Densely Functionalized Dibenzofurans via ZnCl 2 -Mediated Cascade Annulation

inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02841openalex-snapshot

Lanthanum-Catalyzed Regioselective Synthesis of 1- or 4-Functionalized Dibenzofurans via Aryne Intermediates

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00840openalex-snapshot

Accessing Polyoxygenated Dibenzofurans via the Union of Phenols and o-Benzoquinones: Rapid Syntheses of Metabolites Isolated from Ribes takare

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00454openalex-snapshot

Trematosphones A and B, Two Unique Dimeric Structures from the Desert Plant Endophytic Fungus Trematosphaeria terricola

inferred← citeshttps://doi.org/10.1038/s42004-021-00478-2openalex-snapshot

A cascade double 1,4-addition/intramolecular annulation strategy for expeditious assembly of unsymmetrical dibenzofurans

inferred← citeshttps://doi.org/10.1039/c6ra17900bopenalex-snapshot

Isolation of lingzhifuran A and lingzhilactones D–F from Ganoderma lucidum as specific Smad3 phosphorylation inhibitors and total synthesis of lingzhifuran A

inferred← citeshttps://doi.org/10.1039/c7cs00431aopenalex-snapshot

Secondary metabolism in the lichen symbiosis

inferred← citeshttps://doi.org/10.1039/c7nj03799fopenalex-snapshot

Divergent synthesis of 3,4-dihydrodibenzo[ b , d ]furan-1(2 H )-ones and isocoumarins via additive-controlled chemoselective C–C or C–N bond cleavage

inferred← citeshttps://doi.org/10.1039/c8cc10306bopenalex-snapshot

Cascade Rh( ii ) and Yb( iii ) catalyzed synthesis of substituted naphthofurans via transannulation of N -sulfonyl-1,2,3-triazoles with β-naphthols

inferred← citeshttps://doi.org/10.1039/c9ob00690gopenalex-snapshot

Photorearrangement of dihetarylethenes as a tool for the benzannulation of heterocycles

inferred← citeshttps://doi.org/10.1039/d0qo00137fopenalex-snapshot

Efficient access to fluorescent benzofuro[3,2- b ]carbazoles via TFA-promoted cascade annulations of sulfur ylides, 2-hydroxy-β-nitrostyrenes and indoles

inferred← citeshttps://doi.org/10.1039/d0ra01369bopenalex-snapshot

Alumina-promoted oxodefluorination

inferred← citeshttps://doi.org/10.1039/d3cc02054aopenalex-snapshot

Asymmetric total synthesis of (+)-propolisbenzofuran B

inferred← citeshttps://doi.org/10.1039/d4np00011kopenalex-snapshot

Structural diversity and chemical logic underlying the assembly of monoterpene indole alkaloids oligomers

inferred← citeshttps://doi.org/10.1039/d5ob01723hopenalex-snapshot

Arylsulfone-driven divergence in base-mediated [3 + 3] benzannulation reactions of aurones: facile synthesis of substituted dibenzofurans

inferred← citeshttps://doi.org/10.1039/d6qo01110aopenalex-snapshot

Acid- and visible-light-induced skeletal transformation of oxapropellanes into π-extended dibenzofurans

inferred← citeshttps://doi.org/10.1080/00397911.2016.1235201openalex-snapshot

Simple and efficient synthesis of various dibenzofuran carbaldehydes

inferred← citeshttps://doi.org/10.1080/14786419.2022.2036146openalex-snapshot

Dibenzofurans from Crataegus oresbia and their lipid-lowering activity

inferred← citeshttps://doi.org/10.1088/1755-1315/1445/1/012024openalex-snapshot

Antimicrobial and antioxidant properties of the lichens Coccocarpia palmicola, Parmotrema clavuliferum and Parmotrema tinctorum

inferred← citeshttps://doi.org/10.1101/2025.01.07.631633openalex-snapshot

Molecular docking, validation, dynamic simulation and pharmacokinetic prediction of natural compounds against Mycobacterium tuberculosis Beta-lactamase BlaC

inferred← citeshttps://doi.org/10.1111/jam.14239openalex-snapshot

A metabolite of endophytic fungus Cadophora orchidicola from Kalimeris indica serves as a potential fungicide and TLR 4 agonist

inferred← citeshttps://doi.org/10.1177/14690667241229910openalex-snapshot

Structure analysis of depsides, dibenzofuran and sugar derivatives from Cladia aggregata (SW) Nyl using ultra-performance liquid chromatography–tandem mass spectrometry

inferred← citeshttps://doi.org/10.13057/biodiv/d250431openalex-snapshot

Lichen diversity and taxonomy in Bukit Barisan Grand Forest Park, North Sumatra, Indonesia

inferred← citeshttps://doi.org/10.1639/0007-2745-120.1.097openalex-snapshot

Recent literature on lichens—244

inferred← citeshttps://doi.org/10.2139/ssrn.6210928openalex-snapshot

New dibenzofurans and sesquiterpenoid from Phellinus ribis and their anti-inflammatory activity

inferred← citeshttps://doi.org/10.2174/1570180817999201110114107openalex-snapshot

Novel N-(2-Methoxydibenzofuran-3-yl)-2-aryloxyacetamide Derivatives: Synthesis and Biological Investigation

inferred← citeshttps://doi.org/10.30616/ajb.371020openalex-snapshot

Use of lichens as natural insecticide

inferred← citeshttps://doi.org/10.3389/ffunb.2023.1088966openalex-snapshot

Tridepsides as potential bioactives: a review on their chemistry and the global distribution of their lichenic and non-lichenic natural sources

inferred← citeshttps://doi.org/10.3389/fmicb.2017.01251openalex-snapshot

A Novel Derivative of (-)mycousnine Produced by the Endophytic Fungus Mycosphaerella nawae, Exhibits High and Selective Immunosuppressive Activity on T Cells

inferred← citeshttps://doi.org/10.3389/fphar.2018.00265openalex-snapshot

Identification of Novel Melanin Synthesis Inhibitors From Crataegus pycnoloba Using an in Vivo Zebrafish Phenotypic Assay

inferred← citeshttps://doi.org/10.3389/fpls.2026.1792494openalex-snapshot

Poikilohydria, polyols, and homeoviscosity: lichen metabolomic remodeling across environmental gradients

inferred← citeshttps://doi.org/10.3390/f16091364openalex-snapshot

Little Giants: Lichens in Tropical Dry Forests

inferred← citeshttps://doi.org/10.3390/ijms27198621openalex-snapshot

The Reindeer’s Secret: Salazinic Acid from Lichens as a Candidate Modulator of Autophagy

inferred← citeshttps://doi.org/10.3390/jof11050369openalex-snapshot

A Comprehensive Review on Chemical Structures and Bioactivities of Ostropomycetidae Lichens

inferred← citeshttps://doi.org/10.3390/jof12070526openalex-snapshot

Chemo-Diversity and Secondary Metabolite Content in Corticolous Crustose Lichens (Fam. Arthoniaceae, Graphidaceae, Pyrenulaceae) from Remnants of Colombian Tropical Dry Forests

inferred← citeshttps://doi.org/10.3390/md17070422openalex-snapshot

Mycousfurans A and B, Antibacterial Usnic Acid Congeners from the Fungus Mycosphaerella sp., Isolated from a Marine Sediment

inferred← citeshttps://doi.org/10.3390/md19090492openalex-snapshot

Secondary Metabolites with α-Glucosidase Inhibitory Activity from Mangrove Endophytic Fungus Talaromyces sp. CY-3

inferred← citeshttps://doi.org/10.3390/molecules26216572openalex-snapshot

Dibenzofuran Derivatives Inspired from Cercosporamide as Dual Inhibitors of Pim and CLK1 Kinases

inferred← citeshttps://doi.org/10.3390/molecules28104145openalex-snapshot

Unravelling Novel Phytochemicals and Anticholinesterase Activity in Irish Cladonia portentosa

inferred← citeshttps://doi.org/10.36547/nbc.1075openalex-snapshot

Biologically active orcinol-based secondary metabolites originated from lichens

inferred← citeshttps://doi.org/10.51753/flsrt.1572004openalex-snapshot

Exploring the antioxidant and protective effects of usnic acid: Opportunities and challenges

inferred← citeshttps://doi.org/10.59761/rcr5163openalex-snapshot

Benzoannulation of aromatic heterocycles: advances in the 21st century

inferred← citeshttps://doi.org/10.70675/166c106fzf0d3z4b56za4e4z9a9ed49abbddopenalex-snapshot

Antibiofilm activity of lichen secondary metabolites

inferred← citeshttps://doi.org/10.70675/69c906a4z8a84z4595zbe8bz1f87507c0b52openalex-snapshot

Études phytochimiques du lichen Nephroma laevigatum et de ses champignons endolichéniques. Évaluation des activités antiprolifératives et anti-biofilms.

inferred← citeshttps://doi.org/10.70675/bbf65733z42e5z4a36zb197za2838995449aopenalex-snapshot

Études des relations entre leshmanioses et cancers : Leishmania infantum : recherche de sanctuaires de persistance et criblage in vitro de nouvelles molécules actives

inferred← citeshttps://doi.org/10.7150/jca.77588openalex-snapshot

Porric acid E, a natural compound from Rhytidhysteron sp. BZM-9, suppresses colorectal cancer growth via an autophagy-dependent pathway

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