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Protoilludane, Illudane, Illudalane, and Norilludane Sesquiterpenoids from Granulobasidium vellereum

https://doi.org/10.1021/acs.jnatprod.6b00325
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What this work says

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

inferredcites →https://doi.org/10.1002/(sici)1521-3773(19990517)38:10<1328::aid-anie1328>3.0.co;2-1openalex-snapshot
Strobilurins: Evolution of a New Class of Active Substances
inferredcites →https://doi.org/10.1007/978-1-4899-4513-6openalex-snapshot
Dictionary of Terpenoids
inferredcites →https://doi.org/10.1007/s10886-011-9918-3openalex-snapshot
Leaf Chemistry and Foliage Avoidance by the Thrips Frankliniella occidentalis and Heliothrips haemorrhoidalis in Glasshouse Collections
inferredcites →https://doi.org/10.1016/j.jmr.2003.08.009openalex-snapshot
Compensation of refocusing inefficiency with synchronized inversion sweep (CRISIS) in multiplicity-edited HSQC
inferredcites →https://doi.org/10.1016/j.phytochem.2005.06.018openalex-snapshot
Illudalane sesquiterpenoids, echinolactones A and B, from a mycelial culture of Echinodontium japonicum
inferredcites →https://doi.org/10.1016/j.phytochem.2010.11.005openalex-snapshot
Erinea formation on Quercus ilex leaves: Anatomical, physiological and chemical responses of leaf trichomes against mite attack
inferredcites →https://doi.org/10.1016/j.phytochem.2013.02.015openalex-snapshot
Protoilludane sesquiterpenes from the wood decomposing fungus Granulobasidium vellereum (Ellis & Cragin) Jülich
inferredcites →https://doi.org/10.1016/j.phytochem.2014.03.012openalex-snapshot
Sesquiterpenes from the saprotrophic fungus Granulobasidium vellereum (Ellis & Cragin) Jülich
inferredcites →https://doi.org/10.1016/j.tet.2011.12.006openalex-snapshot
Three new diterpenes from Jatropha curcas
inferredcites →https://doi.org/10.1016/j.tet.2012.02.021openalex-snapshot
Two new sesquiterpenes and six norsesquiterpenes from the solid culture of the edible mushroom Flammulina velutipes
inferredcites →https://doi.org/10.1016/s0040-4020(03)00738-5openalex-snapshot
Isolation and structure elucidation of new sesquiterpenes of protoilludane origin from the fungus Clavicorona divaricata
inferredcites →https://doi.org/10.1016/s0040-4020(98)00613-9openalex-snapshot
Isolation and structure elucidation of tsugicolines F-H, novel furosesquiterpenes, and tsugicoline I from the fungus Laurilia tsugicola
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00500openalex-snapshot
Cytotoxic Illudane Sesquiterpenes from the Fungus Granulobasidium vellereum (Ellis and Cragin) Jülich
inferredcites →https://doi.org/10.1021/jo991740xopenalex-snapshot
Illudalane Sesquiterpenoids from the Soft Coral Alcyonium paessleri: The First Natural Nitrate Esters
inferredcites →https://doi.org/10.1021/np070305sopenalex-snapshot
Benzaldehyde Derivatives from Sarcodontia crocea
inferredcites →https://doi.org/10.1021/np300799nopenalex-snapshot
Jatropholane-Type Diterpenes from Euphorbia sikkimensis
inferredcites →https://doi.org/10.1021/np800292nopenalex-snapshot
Detection of VM55599 and Preparaherquamide from Aspergillus japonicus and Penicillium fellutanum: Biosynthetic Implications
inferredcites →https://doi.org/10.1021/ol034565mopenalex-snapshot
Modular, Parallel Synthesis of an Illudinoid Combinatorial Library
inferredcites →https://doi.org/10.1021/ol302468aopenalex-snapshot
Conosilane A, an Unprecedented Sesquiterpene from the Cultures of Basidiomycete Conocybe siliginea
inferredcites →https://doi.org/10.1038/ja.2007.36openalex-snapshot
Serialynic Acid, a New Phenol with an Isopentenyne Side Chain from Antrodia serialis
inferredcites →https://doi.org/10.1111/j.1744-7348.1995.tb07615.xopenalex-snapshot
A method to test compounds for feeding deterrence towards redlegged earth mite (Acarina: Penthaleidae)
inferredcites →https://doi.org/10.1139/v89-065openalex-snapshot
Coprinolone and Δ6-coprinolone: new sesquiterpenes from Coprinus psychromorbidus
inferredcites →https://doi.org/10.1248/cpb.57.311openalex-snapshot
Russujaponols G-L, Illudoid Sesquiterpenes, and Their Neurite Outgrowth Promoting Activity from the Fruit Body of Russula japonica
inferredcites →https://doi.org/10.1515/znb-2006-1017openalex-snapshot
Echinolactones C and D: Two Illudalane Sesquiterpenoids Isolated from the Cultured Mycelia of the Fungus Echinodontium japonicum
inferredcites →https://doi.org/10.1515/znc-1998-11-1201openalex-snapshot
Five New Bioactive Sesquiterpenes from the Fungus Radulomyces confluens (Fr.) Christ
inferredcites →https://doi.org/10.1515/znc-2006-9-1009openalex-snapshot
New Bioactive Sesquiterpenes from Ripartites metrodii and R. tricholoma
inferredcites →https://doi.org/10.3390/molecules190914195openalex-snapshot
Cytotoxic Illudalane Sesquiterpenes from the Wood-Decay Fungus Granulobasidium vellereum (Ellis & Cragin) Jülich
inferredcites →https://doi.org/10.5012/bkcs.2012.33.4.1360openalex-snapshot
Tricuspone, a Rearranged Diterpenoid from Salvia tricuspis

What points at this work

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

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Branch blight and dieback of walnut (Juglans regia L.) caused by Rhytidhysteron juglandis sp. nov. and its endophytic biocontrol agent Granulobasidium vellereum
inferred← citeshttps://doi.org/10.1007/978-3-319-59542-9_1openalex-snapshot
Secondary Metabolites from Higher Fungi
inferred← citeshttps://doi.org/10.1007/978-3-319-71740-1_8openalex-snapshot
Secondary Metabolites of Basidiomycetes
inferred← citeshttps://doi.org/10.1007/978-981-13-5862-3_1openalex-snapshot
Bioactive Secondary Metabolites of Basidiomycetes and Its Potential for Agricultural Plant Growth Promotion
inferred← citeshttps://doi.org/10.1016/j.actatropica.2025.107860openalex-snapshot
Association of the components of soil microorganisms and the density of Schistosome-transmitting Oncomelania hupensis
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2017.10.012openalex-snapshot
Granulobasidium vellereum (Ellis &Cragin) Jülich, a promising biological control agent
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2019.01.011openalex-snapshot
Biological and chemical diversity go hand in hand: Basidiomycota as source of new pharmaceuticals and agrochemicals
inferred← citeshttps://doi.org/10.1016/j.bse.2020.104176openalex-snapshot
Sesquiterpene-α-amino acid quaternary ammonium hybrids from Stereum complicatum (Steraceae)
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114592openalex-snapshot
Norsesquiterpenoids from terrestrial and marine organisms: Chemistry, activity and possible biosynthetic pathways (1963–2024)
inferred← citeshttps://doi.org/10.1016/j.phytol.2017.05.017openalex-snapshot
Antimicrobial activity of illudalane and alliacane sesquiterpenes from the mushroom Gloeostereum incarnatum BCC41461
inferred← citeshttps://doi.org/10.1016/j.tet.2019.05.031openalex-snapshot
Total synthesis of (±)-4,8,14-trihydroxyilludala-2,6,8-triene
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132282openalex-snapshot
Total synthesis of the proposed structure of Anti-TMV active tabasesquiterpene A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.11.069openalex-snapshot
Total synthesis of granulodione
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154363openalex-snapshot
Total synthesis of (±)-pterosin M and (±)-onitisin
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155078openalex-snapshot
Synthesis of a common advanced indane intermediate for the formal total synthesis of (±)-puraquinonic acid, (±)-deliquinone, and (±)-russujaponol
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c01229openalex-snapshot
Chamilactones A and B, Sesquiterpenes from the Endophytic Fungus Chaetomium nigricolor F5
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01301openalex-snapshot
Synthesis of Illudinine from Dimedone and Identification of Activity as a Monoamine Oxidase Inhibitor
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00679openalex-snapshot
Unified Divergent Total Syntheses of Illudalane Sesquiterpenes from Granulolactone via a One-Pot Diels–Alder/Oxidative Aromatization
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02626openalex-snapshot
Total Synthesis of (+)-Viridianol, a Marine-Derived Sesquiterpene Embodying the Decahydrocyclobuta[d]indene Framework
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01669openalex-snapshot
Total Synthesis of (Nor)illudalane Sesquiterpenes Based on a C(sp3)–H Activation Strategy
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03356openalex-snapshot
Synthesis of 4,4-Dimethyl-1,6-heptadiyne and Alcyopterosin O
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02511openalex-snapshot
Synthesis of Four Illudalane Sesquiterpenes Utilizing a One-Pot Diels–Alder/Oxidative Aromatization Sequence
inferred← citeshttps://doi.org/10.1021/acsami.4c18094openalex-snapshot
Formulation of Ethyl Cellulose Nanoparticles Encapsulated with Osthole Provides Long-Lasting Plant Protection against a Major Pest Mite
inferred← citeshttps://doi.org/10.1021/jacs.2c03304openalex-snapshot
Collective Synthesis of Illudalane Sesquiterpenes via Cascade Inverse Electron Demand (4 + 2) Cycloadditions of Thiophene S,S-Dioxides
inferred← citeshttps://doi.org/10.1038/s41429-019-0263-zopenalex-snapshot
Rhizophins A and B, new sesquiterpenes from the culture broth of Coprinus rhizophorus
inferred← citeshttps://doi.org/10.1039/c9cc00933gopenalex-snapshot
Divergent total syntheses of five illudalane sesquiterpenes and assignment of the absolute configuration
inferred← citeshttps://doi.org/10.1039/c9qo01087dopenalex-snapshot
Polyoxygenated meroterpenoids and a bioactive illudalane derivative from a co-culture of Armillaria sp. and Epicoccum sp.
inferred← citeshttps://doi.org/10.1515/ncrs-2020-0598openalex-snapshot
Crystal structure of 5,7,7-trimethyl-4,6,7,8-tetrahydrocyclopenta[ g ]isochromen-1(3 H )-one, C 15 H 18 O 2
inferred← citeshttps://doi.org/10.2174/0113852728394187250807061220openalex-snapshot
Ulmus Species: Their Extraction, Structural Diversity, and Pharmacological Properties
inferred← citeshttps://doi.org/10.3390/jof7121026openalex-snapshot
Sesquiterpenoids Specially Produced by Fungi: Structures, Biological Activities, Chemical and Biosynthesis (2015–2020)
inferred← citeshttps://doi.org/10.3390/md19060333openalex-snapshot
Antiproliferative Illudalane Sesquiterpenes from the Marine Sediment Ascomycete Aspergillus oryzae
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