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Diplopimarane, a 20-nor-ent-Pimarane Produced by the Oak Pathogen Diplodia quercivora
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-3765(20001103)6:21<3991::aid-chem3991>3.0.co;2-vopenalex-snapshot
The First Synthesis of (−)-Asperpentyn and Efficient Syntheses of (+)-Harveynone, (+)-Epiepoformin and (−)-Theobroxide
inferredcites →https://doi.org/10.1002/cbdv.201200358openalex-snapshot
Cyclopaldic Acid, Seiridin, and Sphaeropsidin A as Fungal Phytotoxins, and Larvicidal and Biting Deterrents against Aedes aegypti (Diptera: Culicidae): StructureActivity Relationships
inferredcites →https://doi.org/10.1007/s13225-014-0282-9openalex-snapshot
The complex of Diplodia species associated with Fraxinus and some other woody hosts in Italy and Portugal
inferredcites →https://doi.org/10.1016/0031-9422(96)00206-3openalex-snapshot
A phytotoxic pimarane diterpene of Sphaeropsis sapinea f. sp. Cupressi, the pathogen of a canker disease of cypress
inferredcites →https://doi.org/10.1016/j.fct.2006.06.024openalex-snapshot
Toxicity assessment of metabolites of fungal biocontrol agents using two different (Artemia salina and Daphnia magna) invertebrate bioassays
inferredcites →https://doi.org/10.1016/j.mycres.2007.08.018openalex-snapshot
The use of secondary metabolite profiling in chemotaxonomy of filamentous fungi
inferredcites →https://doi.org/10.1016/j.phytochem.2003.11.006openalex-snapshot
Studies on structure–activity relationship of sphaeropsidins A–F, phytotoxins produced by Sphaeropsis sapinea f. sp. cupressi
inferredcites →https://doi.org/10.1016/j.phytochem.2006.12.017openalex-snapshot
Anti-Candida metabolites from endophytic fungi
inferredcites →https://doi.org/10.1016/j.phytochem.2012.01.011openalex-snapshot
Afritoxinones A and B, dihydrofuropyran-2-ones produced by Diplodia africana the causal agent of branch dieback on Juniperus phoenicea
inferredcites →https://doi.org/10.1016/j.phytol.2012.08.011openalex-snapshot
Evaluation of in vitro anticancer activity of sphaeropsidins A–C, fungal rearranged pimarane diterpenes, and semisynthetic derivatives
inferredcites →https://doi.org/10.1016/j.phytol.2014.07.005openalex-snapshot
Bioactivity studies of oxysporone and several derivatives
inferredcites →https://doi.org/10.1016/j.tet.2003.10.065openalex-snapshot
Total synthesis of (+)-epiepoformin and (−)-phyllostine
inferredcites →https://doi.org/10.1016/s0031-9422(02)00015-8openalex-snapshot
Sphaeropsidins D and E, two other pimarane diterpenes, produced in vitro by the plant pathogenic fungus Sphaeropsis sapinea f. sp. cupressi
inferredcites →https://doi.org/10.1016/s0031-9422(97)00006-xopenalex-snapshot
Sphaeropsidins B and C, phytotoxic pimarane diterpenes from Sphaeropsis sapinea f. sp. Cupressi and Diplodia mutila
inferredcites →https://doi.org/10.1016/s0031-9422(97)00897-2openalex-snapshot
Sphaeropsidone and episphaeropsidone, phytotoxic dimedone methylethers produced by Sphaeropsis sapinea f. sp. Cupressi grown in liquid culture
inferredcites →https://doi.org/10.1016/s0040-4020(03)00119-4openalex-snapshot
Total synthesis of (+)-epiepoformin, (+)-epiepoxydon and (+)-bromoxone employing a useful chiral building block, ethyl (1R,2S)-5,5-ethylenedioxy-2-hydroxycyclohexanecarboxylate
inferredcites →https://doi.org/10.1016/s0040-4039(00)99187-1openalex-snapshot
Absolute configurations of marine diterpenes possessing a xenicane skeleton. An application of an advanced mosher's method
inferredcites →https://doi.org/10.1021/ja00772a054openalex-snapshot
Structures of fungal diterpene antibiotics LL-S491.beta. and -.gamma.
inferredcites →https://doi.org/10.1021/jo070806iopenalex-snapshot
Absolute Configuration of Natural Cyclohexene Oxides by Time Dependent Density Functional Theory Calculation of the Optical Rotation: The Absolute Configuration of (−)-Sphaeropsidone and (−)-Episphaeropsidone Revised
inferredcites →https://doi.org/10.1021/np020367copenalex-snapshot
Diplopyrone, a New Phytotoxic Tetrahydropyranpyran-2-one Produced by Diplodia mutila, a Fungus Pathogen of Cork Oak
inferredcites →https://doi.org/10.1021/np050393lopenalex-snapshot
Diplobifuranylones A and B, 5‘-Monosubstituted Tetrahydro-2H-bifuranyl-5-ones Produced by Diplodia corticola, a Fungus Pathogen of Cork Oak
inferredcites →https://doi.org/10.1021/np100873topenalex-snapshot
Ring B Aromatic Norpimarane Glucoside from a Xylaria sp.
inferredcites →https://doi.org/10.1021/np2000864openalex-snapshot
Smardaesidins A–G, Isopimarane and 20-nor-Isopimarane Diterpenoids from Smardaea sp., a Fungal Endophyte of the Moss Ceratodon purpureus
inferredcites →https://doi.org/10.1021/np200625mopenalex-snapshot
In Vitro Antibacterial Activity of Sphaeropsidins and Chemical Derivatives toward Xanthomonas oryzae pv. oryzae, the Causal Agent of Rice Bacterial Blight
inferredcites →https://doi.org/10.1021/ol050287aopenalex-snapshot
Enantioselective Synthesis of (+)- and (−)-Dihydroepiepoformin and (+)-Epiepoformin
inferredcites →https://doi.org/10.1071/ch03037openalex-snapshot
Sphaeropsidin F, a New Pimarane Diterpene Produced in Vitro by the Cypress Pathogen Sphaeropsis sapinea f. sp. Cupressi
inferredcites →https://doi.org/10.1094/pdis-02-11-0123openalex-snapshot
First Report of Diplodia corticola Causing Branch Cankers on Live Oak (Quercus virginiana) in Florida
inferredcites →https://doi.org/10.1094/pdis-07-13-0736-pdnopenalex-snapshot
First Report of Diplodia quercivora Causing Shoot Dieback and Branch Cankers on Live Oak (Quercus virginiana) in the United States
inferredcites →https://doi.org/10.1094/pdis-10-12-0955-pdnopenalex-snapshot
First Report of Neofusicoccum australe and N. luteum Associated with Canker and Dieback of Quercus robur in Portugal
inferredcites →https://doi.org/10.1094/pdis-91-3-0324aopenalex-snapshot
First Report of Canker Disease Caused by Botryosphaeria parva on Cork Oak Trees in Italy
inferredcites →https://doi.org/10.1107/s0021889898007717openalex-snapshot
SIR 97: a new tool for crystal structure determination and refinement
inferredcites →https://doi.org/10.1111/efp.12081openalex-snapshot
Diplodia corticola and Phytophthora cinnamomi: the main pathogens involved in holm oak decline on C aprera I sland ( I taly)
inferredcites →https://doi.org/10.1111/j.1365-3059.2009.02244.xopenalex-snapshot
First report of Diplodia corticola in Greece on kermes oak ( Quercus coccifera )
inferredcites →https://doi.org/10.1111/j.1439-0329.1989.tb00764.xopenalex-snapshot
Dieback of cork oak (Quercus suber) in Catalonia (NE Spain) caused by Botryosphaeria stevensii
inferredcites →https://doi.org/10.1111/j.1439-0329.2007.00526.xopenalex-snapshot
Evaluation of fungicides for the control of Botryosphaeria corticola on cork oak in Catalonia (NE Spain)
inferredcites →https://doi.org/10.1111/j.1439-0329.2008.00579.xopenalex-snapshot
Physiological responses of cork oak and holm oak to infection by fungal pathogens involved in oak decline
inferredcites →https://doi.org/10.1524/zpch.1997.198.part_1_2.281openalex-snapshot
100 and More Basic NMR Experiments, A Practical Course
inferredcites →https://doi.org/10.3852/12-047openalex-snapshot
Identification and pathogenicity of Botryosphaeriaceae species associated with coast live oak ( Quercus agrifolia ) decline in southern California
inferredcites →https://doi.org/10.3852/12-370openalex-snapshot
Diplodia quercivora sp. nov.: a new species of Diplodia found on declining Quercus canariensis trees in Tunisia
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.2022.113302zenodo-depositor-declared
Diplofuranoxin, a disubstituted dihydrofuranone, was produced together with sphaeropsidin A and epi-sphaeropsidone by Diplodia subglobosa, an emerging ash (Fraxinus excelsior L.) pathogen in Europe
inferred← citeshttps://doi.org/10.1002/cbdv.201900398openalex-snapshot
Phytotoxic Diterpenoids from Plants and Microorganisms
inferred← citeshttps://doi.org/10.1002/cbic.202100283openalex-snapshot
Sphaeropsidin A: A Pimarane Diterpene with Interesting Biological Activities and Promising Practical Applications
inferred← citeshttps://doi.org/10.1002/chir.23009openalex-snapshot
Pimarane diterpenes: Natural source, stereochemical configuration, and biological activity
inferred← citeshttps://doi.org/10.1002/ps.4438openalex-snapshot
Inhibition of early development stages of rust fungi by the two fungal metabolites cyclopaldic acid and epi‐epoformin
inferred← citeshttps://doi.org/10.1002/ps.5351openalex-snapshot
Impact of fungal and plant metabolites application on early development stages of pea powdery mildew
inferred← citeshttps://doi.org/10.1002/ps.6989openalex-snapshot
Anthraquinones and their analogues as potential biocontrol agents of rust and powdery mildew diseases of field crops
inferred← citeshttps://doi.org/10.1007/978-981-16-5617-0_10openalex-snapshot
Antagonists and Antibiosis: Game Changer of Agriculture and Health Sector
inferred← citeshttps://doi.org/10.1007/978-981-95-6529-0_10openalex-snapshot
Recent Advances in Entomopathogenic Fungi as Biocontrol Agents in the Management of Insect Pests in Agriculture
inferred← citeshttps://doi.org/10.1007/s00018-015-1902-6openalex-snapshot
Sphaeropsidin A shows promising activity against drug-resistant cancer cells by targeting regulatory volume increase
inferred← citeshttps://doi.org/10.1007/s00044-015-1439-0openalex-snapshot
Papyracillic acid and its derivatives as biting deterrents against Aedes aegypti (Diptera: Culicidae): structure–activity relationships
inferred← citeshttps://doi.org/10.1007/s11101-024-09979-zopenalex-snapshot
The current status on secondary metabolites produced by fungi of the genus Diplodia associated with plants
inferred← citeshttps://doi.org/10.1007/s41348-024-01056-zopenalex-snapshot
Priming of ash saplings with a low virulent Hymenoscyphus fraxineus strain as a possible disease control approach for reducing symptoms of ash dieback
inferred← citeshttps://doi.org/10.1016/b978-0-12-821008-6.00016-5openalex-snapshot
Bioprospecting for secondary metabolites of family Botryosphaeriaceae from a biotechnological perspective
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.11.001openalex-snapshot
Aspergillus candidus is a newly recognized source of sphaeropsidin A: Isolation, semi-synthetic derivatization and anticancer evaluation
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.02.035openalex-snapshot
New sterically-hindered 6th-substituted 3,5-di-tert-butylcatechols/o-quinones with additional functional groups and their triphenylantimony(V) catecholates
inferred← citeshttps://doi.org/10.1016/j.jpba.2017.02.037openalex-snapshot
Application of Mosher’s method for absolute configuration assignment to bioactive plants and fungi metabolites
inferred← citeshttps://doi.org/10.1016/j.phytochem.2016.10.008openalex-snapshot
Bioactive constituents from transformed root cultures of Nepeta teydea
inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.112056openalex-snapshot
Highly oxygenated isoprenylated cyclohexanoids from the fungus Parastagonospora nodorum SN15
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101497openalex-snapshot
The fungal phytotoxin Sphaeropsidin A from Diplodia cupressi induces oxidative stress and autophagy in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.tet.2016.09.008openalex-snapshot
Further secondary metabolites produced by Diplodia corticola, a fungal pathogen involved in cork oak decline
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.08.098openalex-snapshot
Crystal structure and absolute configuration of sphaeropsidin A and its 6-O-p-bromobenzoate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155082openalex-snapshot
A divergent approach to synthesize C7 epoxyquinones from (–)-shikimic acid
inferred← citeshttps://doi.org/10.1021/acs.jafc.5b05170openalex-snapshot
Bioactive Secondary Metabolites Produced by the Oak PathogenDiplodia corticola
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c15866openalex-snapshot
Advances in Biopesticides and Their Role in the Protection of Agrarian Production ‡
inferred← citeshttps://doi.org/10.1021/acs.jafc.8b00256openalex-snapshot
Phytotoxic Metabolites Produced by Diaporthella cryptica , the Causal Agent of Hazelnut Branch Canker
inferred← citeshttps://doi.org/10.1021/acs.jafc.9b06055openalex-snapshot
Hyfraxinic Acid, a Phytotoxic Tetrasubstituted Octanoic Acid, Produced by the Ash (Fraxinus excelsior L.) Pathogen Hymenoscyphus fraxineus Together with Viridiol and Some of Its Analogues
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00365openalex-snapshot
Pinofuranoxins A and B, Bioactive Trisubstituted Furanones Produced by the Invasive Pathogen Diplodia sapinea
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00486openalex-snapshot
Taichunins E–T, Isopimarane Diterpenes and a 20-nor-Isopimarane, from Aspergillus taichungensis (IBT 19404): Structures and Inhibitory Effects on RANKL-Induced Formation of Multinuclear Osteoclasts
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00018openalex-snapshot
Bioactive Diterpenoids from the Leaves of Callicarpa macrophylla
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b01153openalex-snapshot
Aspewentins D–H, 20-Nor-isopimarane Derivatives from the Deep Sea Sediment-Derived Fungus Aspergillus wentii SD-310
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00696openalex-snapshot
Cochliotoxin, a Dihydropyranopyran-4,5-dione, and Its Analogues Produced by Cochliobolus australiensis Display Phytotoxic Activity against Buffelgrass (Cenchrus ciliaris)
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00556openalex-snapshot
Lentiquinones A, B, and C, Phytotoxic Anthraquinone Derivatives Isolated from Ascochyta lentis, a Pathogen of Lentil
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01532openalex-snapshot
Efficient Synthesis of Octahydrophenanthrene Derivatives with Mild Cascade Reactions of Isochromenylium Tetrafluoroborates and Bifunctional Styrenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03611openalex-snapshot
DeepSAT-Driven Discovery of Pimarane Diterpenoids from Arthrinium arundinis with Ulcerative Colitis Inhibitory Activity via NF-κB/MAPK Pathways
inferred← citeshttps://doi.org/10.1021/jf504609wopenalex-snapshot
Effect of Fungal and Plant Metabolites on Broomrapes ( Orobanche and Phelipanche spp.) Seed Germination and Radicle Growth
inferred← citeshttps://doi.org/10.1039/c5np00081eopenalex-snapshot
Fungal phytotoxins with potential herbicidal activity: chemical and biological characterization
inferred← citeshttps://doi.org/10.1039/c5np00087dopenalex-snapshot
Diterpenoids of terrestrial origin
inferred← citeshttps://doi.org/10.1039/c6np00059bopenalex-snapshot
Diterpenoids of terrestrial origin
inferred← citeshttps://doi.org/10.1039/c6ra17638kopenalex-snapshot
20-Nor-isopimarane cycloethers from the deep-sea sediment-derived fungus Aspergillus wentii SD-310
inferred← citeshttps://doi.org/10.1039/d0ob01586eopenalex-snapshot
Deciphering the chemical instability of sphaeropsidin A under physiological conditions – degradation studies and structural elucidation of the major metabolite
inferred← citeshttps://doi.org/10.1039/d0ra02485fopenalex-snapshot
Sarcosenones A–C, highly oxygenated pimarane diterpenoids from an endolichenic fungus Sarcosomataceae sp.
inferred← citeshttps://doi.org/10.1039/d3np00035dopenalex-snapshot
The incredible story of ophiobolin A and sphaeropsidin A: two fungal terpenes from wilt-inducing phytotoxins to promising anticancer compounds
inferred← citeshttps://doi.org/10.1039/d3ob00005bopenalex-snapshot
20- nor -Isopimarane and isopimarane diterpenoids produced by Aspergillus sp. WT03
inferred← citeshttps://doi.org/10.1080/14786419.2017.1385018openalex-snapshot
Antimould microbial and plant metabolites with potential use in intelligent food packaging
inferred← citeshttps://doi.org/10.1080/14786419.2018.1477154openalex-snapshot
Secondary metabolites produced by Sardiniella urbana, a new emerging pathogen on European hackberry
inferred← citeshttps://doi.org/10.1080/14786419.2024.2426071openalex-snapshot
Pimarane diterpenoids: sources, structures and biological activities
inferred← citeshttps://doi.org/10.1128/aem.00665-24openalex-snapshot
Strong antagonism of an endophyte of Fraxinus excelsior towards the ash dieback pathogen, Hymenoscyphus fraxineus , is mediated by the antifungal secondary metabolite PF1140
inferred← citeshttps://doi.org/10.1177/1934578x1601100940openalex-snapshot
Inhibition of Spore Germination and Appressorium Formation of Rust Species by Plant and Fungal Metabolites
inferred← citeshttps://doi.org/10.1515/chem-2017-0019openalex-snapshot
A survey of bacterial, fungal and plant metabolites against Aedes aegypti (Diptera: Culicidae), the vector of yellow and dengue fevers and Zika virus
inferred← citeshttps://doi.org/10.3389/fmicb.2018.00612openalex-snapshot
Fungal Diversity and Community Composition of Culturable Fungi in Stanhopea trigrina Cast Gibberellin Producers
inferred← citeshttps://doi.org/10.3389/fpls.2022.1098673openalex-snapshot
Combatting insects mediated biotic stress through plant associated endophytic entomopathogenic fungi in horticultural crops
inferred← citeshttps://doi.org/10.3390/biom13111632openalex-snapshot
Bioactive Compounds from an Endophytic Pezicula sp. Showing Antagonistic Effects against the Ash Dieback Pathogen
inferred← citeshttps://doi.org/10.3390/iocag2022-12216openalex-snapshot
Defensive Mutualism of Endophytic Fungi: Effects of Sphaeropsidin A against a Model Lepidopteran Pest
inferred← citeshttps://doi.org/10.3390/molecules23040834openalex-snapshot
Fungal Metabolites Antagonists towards Plant Pests and Human Pathogens: Structure-Activity Relationship Studies
inferred← citeshttps://doi.org/10.3390/molecules23071529openalex-snapshot
(+)-epi-Epoformin, a Phytotoxic Fungal Cyclohexenepoxide: Structure Activity Relationships
inferred← citeshttps://doi.org/10.3390/molecules27072327openalex-snapshot
Secondary Metabolites, including a New 5,6-Dihydropyran-2-One, Produced by the Fungus Diplodia corticola. Aphicidal Activity of the Main Metabolite, Sphaeropsidin A
inferred← citeshttps://doi.org/10.3390/plants10030543openalex-snapshot
Allelopathic Effect of Quercetin, a Flavonoid from Fagopyrum esculentum Roots in the Radicle Growth of Phelipanche ramosa: Quercetin Natural and Semisynthetic Analogues Were Used for a Structure-Activity Relationship Investigation
inferred← citeshttps://doi.org/10.3390/toxins12070444openalex-snapshot
Anti-Biofilm Activity of the Fungal Phytotoxin Sphaeropsidin A against Clinical Isolates of Antibiotic-Resistant Bacteria
inferred← citeshttps://doi.org/10.3390/toxins13040285openalex-snapshot
Activity of Some Plant and Fungal Metabolites towards Aedes albopictus (Diptera, Culicidae)
inferred← citeshttps://doi.org/10.3390/toxins14060407openalex-snapshot
An Ecotoxicological Evaluation of Four Fungal Metabolites with Potential Application as Biocides for the Conservation of Cultural Heritage
inferred← citeshttps://doi.org/10.36253/phyto-14711openalex-snapshot
Current status of Botryosphaeriaceae species in Italy: Impacts on agricultural crops and forest ecosystems
inferred← citeshttps://doi.org/10.64898/2025.12.19.695327openalex-snapshot
Modulation of translational elongation by montanine alkaloids preferentially inhibits RNA viruses
inferred← citeshttps://doi.org/10.70675/037937cez3f01z4fb9z88f6z8d0c4a621b61openalex-snapshot
Optimisation de la production d’effecteurs de Botryosphaeriacées pour maîtriser leur phytopathogénicité et exploiter leurs enzymes pour le bioraffinage du végétal.
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