On the public citation graph
https://doi.org/10.1021/jo00377a007
0 signed · 33 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known work and none has been retracted — and get a dated CiteStamped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 points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4693901openalex-extracted
Four Undescribed Coumarins from Notopterygium Incisum
inferred← citeshttps://doi.org/10.1002/cbdv.202300424openalex-snapshot
Cyclohexenone Derivative and Drimane Sesquiterpenes from the Seagrass‐Derived Fungus Aspergillus insuetus
inferred← citeshttps://doi.org/10.1002/chin.198728222openalex-snapshot
ChemInform Abstract: Isolation of Macrocyclic Trichothecenes from a Large‐Scale Extract of Baccharis megapotamica.
inferred← citeshttps://doi.org/10.1002/pca.2800030602openalex-snapshot
Macrocyclic trichothecenes from brazilian Baccharis species: From microanalysis to large‐scale isolation
inferred← citeshttps://doi.org/10.1007/978-3-030-83511-8_14openalex-snapshot
Macrocyclic Trichothecenes of Baccharis
inferred← citeshttps://doi.org/10.1007/978-3-211-49389-2_2openalex-snapshot
The Trichothecenes and Their Biosynthesis
inferred← citeshttps://doi.org/10.1007/bf00194364openalex-snapshot
Growth hormone-like activities of macrocyclic trichothecenes in in vitro callus induction and growth of four Baccharis species
inferred← citeshttps://doi.org/10.1007/bf01062363openalex-snapshot
Effects of macrocyclic trichothecene mycotoxins on the murine immune system
inferred← citeshttps://doi.org/10.1016/0031-9422(91)85253-vopenalex-snapshot
Trichothecene mycotoxins from Brazilian Baccharis species
inferred← citeshttps://doi.org/10.1016/0041-0101(92)90444-aopenalex-snapshot
The toxicity of macrocyclic trichothecenes administered directly into the rat brain
inferred← citeshttps://doi.org/10.1016/0378-4274(89)90185-9openalex-snapshot
Comparison of the toxicity of two trichothecenes applied topically to brain and liver of rats
inferred← citeshttps://doi.org/10.1016/0378-4274(90)90252-hopenalex-snapshot
Effects of macrocyclic trichothecene congeners on the viability and mitogenesis of murine splenic lymphocytes
inferred← citeshttps://doi.org/10.1016/b978-0-08-036139-0.50007-5openalex-snapshot
MYCOTOXINS - AN OVERVIEW
inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.112238openalex-snapshot
New tricks for old dogs: Two new macrocyclic trichothecene epimers and absolute configuration of 16-hydroxyverrucarin B
inferred← citeshttps://doi.org/10.1016/s0021-9673(01)89632-1openalex-snapshot
Chromatographic methods as tools in the field of mycotoxins
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)83437-2openalex-snapshot
The NMR spectra of trichothecenes and related fungal metabolites
inferred← citeshttps://doi.org/10.1016/s0301-4770(08)60567-9openalex-snapshot
Chapter 7 Thin-Layer Chromatography of Mycotoxins
inferred← citeshttps://doi.org/10.1016/s0301-4770(08)60568-0openalex-snapshot
Chapter 8 Liquid Column Chromatography of Mycotoxins
inferred← citeshttps://doi.org/10.1021/acsomega.0c02489openalex-snapshot
Secondary Metabolites and Bioactivities of Aspergillus ochraceopetaliformis Isolated from Anthurium brownii
inferred← citeshttps://doi.org/10.1039/d4sc00262hopenalex-snapshot
Palladium/XuPhos-catalyzed enantioselective cascade Heck/intermolecular C(sp 2 )–H alkylation reaction
inferred← citeshttps://doi.org/10.1039/d5ob01081kopenalex-snapshot
Rapid construction of furan-linked bisheterocycles via a palladium-catalyzed domino Heck/cross-coupling reaction
inferred← citeshttps://doi.org/10.1070/rc1996v065n05abeh000219openalex-snapshot
Natural aliphatic oxygenated unsaturated acids. Synthesis and biological activity.
inferred← citeshttps://doi.org/10.1107/s2053229624006144openalex-snapshot
Crystal structure of the cytotoxic macrocyclic trichothecene Isororidin A
inferred← citeshttps://doi.org/10.1111/j.1439-0442.1989.tb00715.xopenalex-snapshot
Toxicology of Novel Macrocyclic Trichothecenes, Baccharinoid B4, Myrotoxin B, and Roritoxin B
inferred← citeshttps://doi.org/10.3109/15569549309084187openalex-snapshot
Toxicological Studies with Trichothecenes, Applied to the Rat BrainIn VivoandIn Vitro
inferred← citeshttps://doi.org/10.3389/fmicb.2022.800626openalex-snapshot
Structurally Various Sorbicillinoids From an Endophytic Fungus Acremonium citrinum SS-g13
inferred← citeshttps://doi.org/10.3390/catal10091084openalex-snapshot
Syntheses of 3,3-Disubstituted Dihydrobenzofurans, Indolines, Indolinones and Isochromanes by Palladium-Catalyzed Tandem Reaction Using Pd(PPh3)2Cl2/(±)-BINAP as a Catalytic System
inferred← citeshttps://doi.org/10.3390/md12063116openalex-snapshot
Nine New and Five Known Polyketides Derived from a Deep Sea-Sourced Aspergillus sp. 16-02-1
inferred← citeshttps://doi.org/10.3390/md22010015openalex-snapshot
Pestalotiopols E–J, Six New Polyketide Derivatives from a Marine Derived Fungus Pestalotiopsis sp. SWMU-WZ04-1
inferred← citeshttps://doi.org/10.3390/toxins3121518openalex-snapshot
Current and Future Experimental Strategies for Structural Analysis of Trichothecene Mycotoxins—A Prospectus
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.