On the public citation graph
Pestaloquinols A and B, Isoprenylated Epoxyquinols from Pestalotiopsis sp.
0 signed · 70 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-3773(20020902)41:17<3192::aid-anie3192>3.0.co;2-eopenalex-snapshot
Total Synthesis of (+)-Epoxyquinols A and B
inferredcites →https://doi.org/10.1016/j.bmc.2008.11.066openalex-snapshot
Pestalofones A–E, bioactive cyclohexanone derivatives from the plant endophytic fungus Pestalotiopsis fici
inferredcites →https://doi.org/10.1016/j.tet.2008.03.016openalex-snapshot
Cytosporin-related compounds from the marine-derived fungus Eutypella scoparia
inferredcites →https://doi.org/10.1016/s0031-9422(00)00408-8openalex-snapshot
Ambuic acid, a highly functionalized cyclohexenone with antifungal activity from Pestalotiopsis spp. and Monochaetia sp.
inferredcites →https://doi.org/10.1016/s0040-4039(03)01781-7openalex-snapshot
Reaction modes of oxidative dimerization of epoxycyclohexenols
inferredcites →https://doi.org/10.1021/cr980013jopenalex-snapshot
Naturally Occurring Cyclohexane Epoxides: Sources, Biological Activities, and Synthesis
inferredcites →https://doi.org/10.1021/ja00011a006openalex-snapshot
High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
inferredcites →https://doi.org/10.1021/ja005552wopenalex-snapshot
Total Synthesis of (±)-Torreyanic Acid
inferredcites →https://doi.org/10.1021/ja0127279openalex-snapshot
Epoxyquinol A, a Highly Functionalized Pentaketide Dimer with Antiangiogenic Activity Isolated from Fungal Metabolites
inferredcites →https://doi.org/10.1021/jo0355303openalex-snapshot
Different Reaction Modes for the Oxidative Dimerization of Epoxyquinols and Epoxyquinones. Importance of Intermolecular Hydrogen-Bonding
inferredcites →https://doi.org/10.1021/jo048425hopenalex-snapshot
Total Synthesis of Epoxyquinols A, B, and C and Epoxytwinol A and the Reactivity of a 2H-Pyran Derivative as the Diene Component in the Diels−Alder Reaction
inferredcites →https://doi.org/10.1021/jo050897oopenalex-snapshot
Synthesis of Epoxyquinol A and Related Molecules: Probing Chemical Reactivity of Epoxyquinol Dimers and 2H-Pyran Precursors
inferredcites →https://doi.org/10.1021/jo951736vopenalex-snapshot
Pestalotiopsins A and B: New Caryophyllenes from an Endophytic Fungus of Taxus brevifolia
inferredcites →https://doi.org/10.1021/jo960471xopenalex-snapshot
Torreyanic Acid: A Selectively Cytotoxic Quinone Dimer from the Endophytic Fungus Pestalotiopsis microspora
inferredcites →https://doi.org/10.1021/np020098qopenalex-snapshot
Panepophenanthrin, from a Mushroom Strain, a Novel Inhibitor of the Ubiquitin-Activating Enzyme
inferredcites →https://doi.org/10.1021/np050460bopenalex-snapshot
Caryophyllene Sesquiterpenoids from a Fungicolous Isolate of Pestalotiopsis disseminata
inferredcites →https://doi.org/10.1021/np070590fopenalex-snapshot
Antifungal Metabolites from the Plant Endophytic Fungus Pestalotiopsis foedan
inferredcites →https://doi.org/10.1021/np100071zopenalex-snapshot
Oxepinochromenones, Furochromenone, and their Putative Precursors from the Endolichenic Fungus Coniochaeta sp.
inferredcites →https://doi.org/10.1021/np800733yopenalex-snapshot
Ambuic Acid and Torreyanic Acid Derivatives from the Endolichenic Fungus Pestalotiopsis sp.
inferredcites →https://doi.org/10.1021/np900084dopenalex-snapshot
Photinides A−F, Cytotoxic Benzofuranone-Derived γ-Lactones from the Plant Endophytic Fungus Pestalotiopsis photiniae
inferredcites →https://doi.org/10.1021/np9600053openalex-snapshot
A New Isodrimeninol from Pestalotiopsis sp.
inferredcites →https://doi.org/10.1021/ol026513nopenalex-snapshot
Angiogenesis Inhibitor Epoxyquinol A: Total Synthesis and Inhibition of Transcription Factor NF-κB
inferredcites →https://doi.org/10.1021/ol800136topenalex-snapshot
Chloropupukeananin, the First Chlorinated Pupukeanane Derivative, and Its Precursors from Pestalotiopsis fici
inferredcites →https://doi.org/10.1039/b918330bopenalex-snapshot
Unique metabolites of Pestalotiopsis fici suggest a biosynthetic hypothesis involving a Diels–Alder reaction and then mechanistic diversification
inferredcites →https://doi.org/10.1271/bbb.62.1624openalex-snapshot
Pesthetoxin, a New Phytotoxin Produced by the Gray Blight Fungus,Pestalotiopsis theae
inferredcites →https://doi.org/10.7164/antibiotics.55.829openalex-snapshot
Epoxyquinol B, a Fungal Metabolite with a Potent Antiangiogenic Activity.
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.2022.113124zenodo-depositor-declared
Prenylated cyclohexene-type meroterpenoids and sulfur-containing xanthones produced by Pseudopestalotiopsis theae
inferred← citeshttps://doi.org/10.1002/ejoc.201200007openalex-snapshot
α‐Pyrones and Pyranes from the Plant Pathogenic Fungus Pestalotiopsis scirpina
inferred← citeshttps://doi.org/10.1002/ejoc.201200053openalex-snapshot
Trichoderones A and B: Two Pentacyclic Cytochalasans from the Plant Endophytic Fungus Trichoderma gamsii
inferred← citeshttps://doi.org/10.1002/med.21348openalex-snapshot
Toward a Cancer Drug of Fungal Origin
inferred← citeshttps://doi.org/10.1007/978-81-322-1801-2_5openalex-snapshot
Fungal Endophytes: An Amazing and Hidden Source of Cytotoxic Compounds
inferred← citeshttps://doi.org/10.1007/s11101-017-9495-3openalex-snapshot
Recent advances in the discovery of bioactive metabolites from Pestalotiopsis
inferred← citeshttps://doi.org/10.1007/s12272-023-01453-2openalex-snapshot
Recent advances on Pestalotiopsis genus: chemistry, biological activities, structure–activity relationship, and biosynthesis
inferred← citeshttps://doi.org/10.1007/s13225-014-0288-3openalex-snapshot
Chemistry and biology of Pestalotiopsis-derived natural products
inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.21118-7openalex-snapshot
Antitumor and Immunomodulatory Compounds from Fungi
inferred← citeshttps://doi.org/10.1016/b978-0-12-821006-2.00007-8openalex-snapshot
Fungal secondary metabolites: A potential source of anticancer compounds
inferred← citeshttps://doi.org/10.1016/b978-0-12-824523-1.00015-8openalex-snapshot
Endophytic fungi as a potential source of cytotoxic drugs: a fungal solution to cancer
inferred← citeshttps://doi.org/10.1016/b978-0-444-53836-9.00025-6openalex-snapshot
Diversity and Ecological Significance of Fungal Endophyte Natural Products
inferred← citeshttps://doi.org/10.1016/j.fitote.2011.12.021openalex-snapshot
Trichalasins C and D from the plant endophytic fungus Trichoderma gamsii
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.03.020openalex-snapshot
Two spiroketal derivatives with an unprecedented amino group and their cytotoxicity evaluation from the endophytic fungus Pestalotiopsis flavidula
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.06.009openalex-snapshot
Polyketide derivatives from a marine-sponge-associated fungus Pestalotiopsis heterocornis
inferred← citeshttps://doi.org/10.1016/j.tet.2013.05.075openalex-snapshot
A total synthesis of the epoxyquinone natural product cytosporin D
inferred← citeshttps://doi.org/10.1016/j.tet.2014.12.009openalex-snapshot
Meroterpenoid, isocoumarin, and phenol derivatives from the seagrass-derived fungus Pestalotiopsis sp. PSU-ES194
inferred← citeshttps://doi.org/10.1016/j.tet.2017.09.030openalex-snapshot
Progress in the total synthesis of epoxyquinone natural products: An update
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.05.115openalex-snapshot
Enantioselective syntheses of bioactive epoxyquinone natural products (+)-harveynone and (−)-asperpentyn
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.10.005openalex-snapshot
Cytosporins F–K, new epoxyquinols from the endophytic fungus Pestalotiopsis theae
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153314openalex-snapshot
Antibacterial secondary metabolites from the endophytic fungus Eutypella scoparia SCBG-8
inferred← citeshttps://doi.org/10.1016/s1875-5364(13)60036-9openalex-snapshot
Natural products chemistry research: progress in China in 2011
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01403openalex-snapshot
Organophotocatalytic Radical Chloro-fluorosulfonylation of Alkynyl Cyclohexadienones
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00962openalex-snapshot
Cuautepestalorin, a 7,8-Dihydrochromene–Oxoisochromane Adduct Bearing a Hexacyclic Scaffold from Pestalotiopsis sp. IQ-011
inferred← citeshttps://doi.org/10.1021/np4007487openalex-snapshot
Trichodermone, a Spiro-cytochalasan with a Tetracyclic Nucleus (7/5/6/5) Skeleton from the Plant Endophytic Fungus Trichoderma gamsii
inferred← citeshttps://doi.org/10.1021/np5004615openalex-snapshot
Biosynthetic Origins of the Epoxyquinone Skeleton in Epoxyquinols A and B
inferred← citeshttps://doi.org/10.1038/ja.2011.124openalex-snapshot
Cytochalasans with different amino-acid origin from the plant endophytic fungus Trichoderma gamsii
inferred← citeshttps://doi.org/10.1038/ja.2012.14openalex-snapshot
Photipyrones A and B, new pyrone derivatives from the plant endophytic fungus Pestalotiopsis photiniae
inferred← citeshttps://doi.org/10.1038/ja.2013.70openalex-snapshot
Stereochemical determination of a new and cytotoxic euphane triterpenoid from the plant endophytic fungus Phomopsis chimonanthi
inferred← citeshttps://doi.org/10.1039/c2np00073copenalex-snapshot
The taxonomy, biology and chemistry of the fungal Pestalotiopsis genus
inferred← citeshttps://doi.org/10.1039/c2ob25469gopenalex-snapshot
Isolation, antimicrobial activity, and absolute configuration of the furylidene tetronic acid core of pestalotic acids A–G
inferred← citeshttps://doi.org/10.1039/d2ra03717copenalex-snapshot
Iron salt-promoted oxidation of steroidal phenols by m -chloroperbenzoic acid: a route to possible antitumor agents
inferred← citeshttps://doi.org/10.1039/d5ob00115copenalex-snapshot
DMSO enhances the biosynthesis of epoxyquinols in Pestalotiopsis sp. (strain IQ-011) and yields new [4 + 2] cycloaddition dimers
inferred← citeshttps://doi.org/10.1080/10286020.2011.621422openalex-snapshot
Two new compounds from an endophytic fungusPestalotiopsis heterocornis
inferred← citeshttps://doi.org/10.1080/10286020.2022.2132480openalex-snapshot
Two ambuic acid dimers derived from homo-endo Diels-Alder reaction from Pestalotiopsis versicolor
inferred← citeshttps://doi.org/10.1080/21501203.2011.562248openalex-snapshot
Bioactive metabolites from the plant endophytePestalotiopsis fici
inferred← citeshttps://doi.org/10.1155/2017/6961928openalex-snapshot
Polyketide-Terpene Hybrid Metabolites from an Endolichenic Fungus Pestalotiopsis sp.
inferred← citeshttps://doi.org/10.3390/md18020129openalex-snapshot
Polyketide Derivatives from Mangrove Derived Endophytic Fungus Pseudopestalotiopsis theae
inferred← citeshttps://doi.org/10.3390/molecules17078554openalex-snapshot
Two New Oxysporone Derivatives from the Fermentation Broth of the Endophytic Plant Fungus Pestalotiopsis karstenii Isolated from Stems of Camellia sasanqua
inferred← citeshttps://doi.org/10.3390/molecules18022236openalex-snapshot
New Spiral γ-Lactone Enantiomers from the Plant Endophytic Fungus Pestalotiopsis foedan
inferred← citeshttps://doi.org/10.3390/molecules180910944openalex-snapshot
Chaetochromones A and B, Two New Polyketides from the Fungus Chaetomium indicum (CBS.860.68)
inferred← citeshttps://doi.org/10.3390/molecules26237229openalex-snapshot
Five New Terpenes with Cytotoxic Activity from Pestalotiopsis sp.
inferred← citeshttps://doi.org/10.3390/molecules27228088openalex-snapshot
Pestalotiopsis Diversity: Species, Dispositions, Secondary Metabolites, and Bioactivities
inferred← citeshttps://doi.org/10.4028/www.scientific.net/amm.303-306.2598openalex-snapshot
Research on the Inhibitory Activity of Endophytic Fungi in Huperzia serrata against AchE
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.