On the public citation graph

Harzianone Biosynthesis by the Biocontrol Fungus Trichoderma

0 signed · 68 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/ange.201209173openalex-snapshot
Eine Nahaufnahme der 2‐Methylisoborneol‐Biosynthese
inferredcites →https://doi.org/10.1002/ange.201501765openalex-snapshot
Strukturrevision und Aufklärung der Biosynthese von Hypodoratoxid durch ein 13C,13C‐COSY‐NMR‐Experiment
inferredcites →https://doi.org/10.1002/ange.201603782openalex-snapshot
Mechanistische Charakterisierung von zwei Sesquiterpen‐Cyclasen aus dem phytopathogenen Pilz Fusarium fujikuroi
inferredcites →https://doi.org/10.1002/ange.201605425openalex-snapshot
Pristinol, ein Sesquiterpen‐Alkohol mit ungewöhnlichem Gerüst aus Streptomyces pristinaespiralis
inferredcites →https://doi.org/10.1002/anie.201209173openalex-snapshot
A Detailed View of 2‐Methylisoborneol Biosynthesis
inferredcites →https://doi.org/10.1002/anie.201501765openalex-snapshot
Structural Revision and Elucidation of the Biosynthesis of Hypodoratoxide by 13C,13C COSY NMR Spectroscopy
inferredcites →https://doi.org/10.1002/anie.201603782openalex-snapshot
Mechanistic Characterisation of Two Sesquiterpene Cyclases from the Plant Pathogenic Fungus Fusarium fujikuroi
inferredcites →https://doi.org/10.1002/anie.201605425openalex-snapshot
Pristinol, a Sesquiterpene Alcohol with an Unusual Skeleton from Streptomyces pristinaespiralis
inferredcites →https://doi.org/10.1002/anie.201608971openalex-snapshot
Terpene Cyclases from Social Amoebae
inferredcites →https://doi.org/10.1002/anie.201612439openalex-snapshot
Mechanistic Investigations of Two Bacterial Diterpene Cyclases: Spiroviolene Synthase and Tsukubadiene Synthase
inferredcites →https://doi.org/10.1002/cbic.200300813openalex-snapshot
Biosynthesis of Volatiles by the Myxobacterium Myxococcus xanthus
inferredcites →https://doi.org/10.1002/cbic.201300254openalex-snapshot
PR Toxin Biosynthesis in Penicillium roqueforti
inferredcites →https://doi.org/10.1002/cbic.201402298openalex-snapshot
Pogostol Biosynthesis by the Endophytic Fungus Geniculosporium
inferredcites →https://doi.org/10.1002/chem.201702704openalex-snapshot
Mechanisms of the Diterpene Cyclases β‐Pinacene Synthase from Dictyostelium discoideum and Hydropyrene Synthase from Streptomyces clavuligerus
inferredcites →https://doi.org/10.1002/ejoc.201100188openalex-snapshot
Synthesis of Deuterated Mevalonolactone Isotopomers
inferredcites →https://doi.org/10.1002/ejoc.201100688openalex-snapshot
Enantioselective Synthesis of the Unnatural Enantiomers of the Fungal Sesquiterpenoids Acorenone and Trichoacorenol
inferredcites →https://doi.org/10.1002/ejoc.201300049openalex-snapshot
2H‐Pyran‐2‐ones from Trichoderma viride and Trichoderma asperellum
inferredcites →https://doi.org/10.1002/jlcr.2580251104openalex-snapshot
New stereospecific labeling of mevalonolactone at position C‐5 with deuterium and tritium
inferredcites →https://doi.org/10.1007/s11101-006-9032-2openalex-snapshot
Secondary metabolites from species of the biocontrol agent Trichoderma
inferredcites →https://doi.org/10.1016/0021-9673(76)80005-2openalex-snapshot
Stripping of trace organic substances from water
inferredcites →https://doi.org/10.1016/0031-9422(75)85255-1openalex-snapshot
The characterization of 6-(pent-1-enyl)-α-pyrone from Trichoderma viride
inferredcites →https://doi.org/10.1016/b978-0-444-59576-8.00010-2openalex-snapshot
Secondary Metabolism and Antimicrobial Metabolites of Trichoderma
inferredcites →https://doi.org/10.1016/j.phytochem.2013.10.016openalex-snapshot
Bicyclic and tetracyclic diterpenes from a Trichoderma symbiont of Taxus baccata
inferredcites →https://doi.org/10.1016/j.soilbio.2007.07.002openalex-snapshot
Trichoderma–plant–pathogen interactions
inferredcites →https://doi.org/10.1016/s0007-1536(87)80034-7openalex-snapshot
Antifungal alkyl pyrones of Trichoderma harzianum
inferredcites →https://doi.org/10.1016/s0040-4020(97)00024-0openalex-snapshot
A new fungal growth inhibitor from Trichoderma viride
inferredcites →https://doi.org/10.1021/ja00397a045openalex-snapshot
Stereochemical studies of isoprenoid biosynthesis. Biosynthesis of pentalenolactone from [U-13C6]glucose and [6-2H2]glucose
inferredcites →https://doi.org/10.1021/ja2055929openalex-snapshot
The Taxadiene-Forming Carbocation Cascade
inferredcites →https://doi.org/10.1021/ja9021649openalex-snapshot
Biosynthesis of the Sesquiterpene Botrydial in Botrytis cinerea. Mechanism and Stereochemistry of the Enzymatic Formation of Presilphiperfolan-8β-ol
inferredcites →https://doi.org/10.1021/jf034708jopenalex-snapshot
Viridepyronone, a New Antifungal 6-Substituted 2H-Pyran-2-one Produced by Trichoderma viride
inferredcites →https://doi.org/10.1021/jf60180a010openalex-snapshot
Characterization of the major aroma constituent of the fungus Trichoderma viride
inferredcites →https://doi.org/10.1021/jo0502091openalex-snapshot
Stereochemistry of the Macrocyclization and Elimination Steps in Taxadiene Biosynthesis through Deuterium Labeling
inferredcites →https://doi.org/10.1021/np50089a023openalex-snapshot
Harziandione, a New Class of Diterpene from Trichoderma harzianum
inferredcites →https://doi.org/10.1021/ol3014717openalex-snapshot
Absolute Configurations of Unique Harziane Diterpenes from Trichoderma Species
inferredcites →https://doi.org/10.1038/154667b0openalex-snapshot
Production of Gliotoxin by Trichoderma viride
inferredcites →https://doi.org/10.1038/nature09628openalex-snapshot
Taxadiene synthase structure and evolution of modular architecture in terpene biosynthesis
inferredcites →https://doi.org/10.1038/nrmicro797openalex-snapshot
Trichoderma species — opportunistic, avirulent plant symbionts
inferredcites →https://doi.org/10.1039/c1ra00212kopenalex-snapshot
Biosynthesis of acorane sesquiterpenes by Trichoderma
inferredcites →https://doi.org/10.1039/c3cc45982aopenalex-snapshot
Labelling studies on the biosynthesis of terpenes in Fusarium fujikuroi
inferredcites →https://doi.org/10.1039/c3ob41755gopenalex-snapshot
The stereochemical course of tricho-acorenol biosynthesis
inferredcites →https://doi.org/10.1039/c4cc00177jopenalex-snapshot
Identification of isoafricanol and its terpene cyclase in Streptomyces violaceusniger using CLSA-NMR
inferredcites →https://doi.org/10.1039/c7np00003kopenalex-snapshot
Fungal volatiles – a survey from edible mushrooms to moulds
inferredcites →https://doi.org/10.1094/phyto-96-0190openalex-snapshot
Overview of Mechanisms and Uses of Trichoderma spp.
inferredcites →https://doi.org/10.1107/s1600536814004632openalex-snapshot
Trichodermaerin: a diterpene lactone fromTrichoderma asperellum
inferredcites →https://doi.org/10.1111/1462-2920.13080openalex-snapshot
Gliotoxin – bane or boon?
inferredcites →https://doi.org/10.1248/cpb.43.1035openalex-snapshot
Studies on Metabolites of Mycoparasitic Fungi. III. New Sesquiterpene Alcohol from Trichoderma koningii.
inferredcites →https://doi.org/10.4265/bio.10.31openalex-snapshot
In Vitro Antifungal and Antiviral Activities of .GAMMA.- and .DELTA.-Lactone Analogs Utilized as Food Flavoring

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.2022.113087zenodo-depositor-declared
(+)- and (−)-trichodermatrione A: a pair of enantiomers with a cyclobutane-containing skeleton from the endophytic fungus Trichoderma sp. EFT2
inferred← citeshttps://doi.org/10.1002/ange.201912982openalex-snapshot
Total Synthesis and Structural Revision of a Harziane Diterpenoid
inferred← citeshttps://doi.org/10.1002/anie.201912982openalex-snapshot
Total Synthesis and Structural Revision of a Harziane Diterpenoid
inferred← citeshttps://doi.org/10.1002/ps.70836openalex-snapshot
Antifungal activity and mechanism of 4‐ethyl‐2‐methoxyphenol from Ceriporia lacerata HG2011 against Colletotrichum camelliae
inferred← citeshttps://doi.org/10.1007/s13659-024-00433-3openalex-snapshot
Chemistry and biology of marine-derived Trichoderma metabolites
inferred← citeshttps://doi.org/10.1016/j.engmic.2022.100058openalex-snapshot
Sustainable biosynthesis of valuable diterpenes in microbes
inferred← citeshttps://doi.org/10.1016/j.phytol.2019.05.001openalex-snapshot
Harziane and cadinane terpenoids from the alga-endophytic fungus Trichoderma asperellum A-YMD-9-2
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00188openalex-snapshot
Proharziane and Harziane Derivatives from the Marine Algicolous Fungus Trichoderma asperelloides RR-dl-6-11
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00714openalex-snapshot
Diterpenes and Sesquiterpenes from the Marine Algicolous Fungus Trichoderma harzianum X-5
inferred← citeshttps://doi.org/10.1021/acs.joc.4c03114openalex-snapshot
Pyrrolidine Alkaloids and Polyketide Derivatives from the Marine-Derived Fungus Trichoderma harzianum ZN-4
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00769openalex-snapshot
Synthetic Strategy for Construction of Highly Congested Tetracyclic Core (6–5–7–4) of Harziane Diterpenoids
inferred← citeshttps://doi.org/10.1021/acscatal.4c05811openalex-snapshot
An Isopentenol Utilization Pathway-Based “Deuterium-Scanning” Method for Mechanistic Investigations of Terpene Cyclases
inferred← citeshttps://doi.org/10.1021/jacs.5c14490openalex-snapshot
Divergent Total Synthesis of the Harziane Diterpenoids
inferred← citeshttps://doi.org/10.1038/s41467-025-63055-4openalex-snapshot
Noncanonical terpene cyclases for the biosynthesis of diterpenoids regulating chlamydospore formation in plant-associated Trichoderma
inferred← citeshttps://doi.org/10.1038/s41598-019-49778-7openalex-snapshot
Potent Phytotoxic Harziane Diterpenes from a Soft Coral-Derived Strain of the Fungus Trichoderma harzianum XS-20090075
inferred← citeshttps://doi.org/10.1039/c7np90051aopenalex-snapshot
Hot off the press
inferred← citeshttps://doi.org/10.1039/c8np00079dopenalex-snapshot
Diterpenoids of terrestrial origin
inferred← citeshttps://doi.org/10.1039/d0ra09627jopenalex-snapshot
Molecular methods unravel the biosynthetic potential of Trichoderma species
inferred← citeshttps://doi.org/10.1039/d5ob01393copenalex-snapshot
Overview of harziane diterpenoids: discovery, bioactivity, total synthesis and biosynthesis
inferred← citeshttps://doi.org/10.3390/jof8030244openalex-snapshot
Diterpenes Specially Produced by Fungi: Structures, Biological Activities, and Biosynthesis (2010–2020)
inferred← citeshttps://doi.org/10.3390/md20110701openalex-snapshot
Structures and Biological Activities of Secondary Metabolites from Trichoderma harzianum
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.