On the public citation graph
Novel Trinor‐eremophilanes (Dendryphiellin B, C, and D), Eremophilanes (Dendryphiellin E, F, and G), and Branched C9‐Carboxylic Acids (Dendryphiellic Acid A and B) from the Marine Deuteromycete Dendryphiella salina (S UTHERLAND ) P UGH et N ICOT
0 signed · 56 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known work and none has been retracted — and get a dated CiteStamped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/cber.19711040614openalex-snapshot
Stereochemie aliphatischer Carbonium‐Ionen, 4. Wasserstoff‐Verschiebung im 2.6‐Dimethyl‐octyl‐System
inferredcites →https://doi.org/10.1002/hlca.19880710107openalex-snapshot
Dendryphiellin A, the First Fungal Trinor‐eremophilane. Isolation from the marine deuteromycete Dendryphiella salina (S UTHERLAND ) P UGH et N ICOT
inferredcites →https://doi.org/10.1016/0022-2364(81)90022-6openalex-snapshot
Correlation of proton chemical shifts by two-dimensional Fourier transform NMR
inferredcites →https://doi.org/10.1016/0022-2364(81)90287-0openalex-snapshot
Investigation of complex networks of spin-spin coupling by two-dimensional NMR
inferredcites →https://doi.org/10.1016/0022-2364(82)90286-4openalex-snapshot
Distortionless enhancement of NMR signals by polarization transfer
inferredcites →https://doi.org/10.1016/0022-2364(83)90225-1openalex-snapshot
Broadband homonuclear decoupling in heteronuclear shift correlation NMR spectroscopy
inferredcites →https://doi.org/10.1016/0022-2364(87)90224-1openalex-snapshot
The nuclear overhauser effect in strongly coupled spin systems
inferredcites →https://doi.org/10.1016/s0040-4039(00)89494-0openalex-snapshot
Dipyridine-chromium(VI) oxide oxidation of alcohols in dichloromethane
inferredcites →https://doi.org/10.1039/c2970000213bopenalex-snapshot
Selective reduction of 2-ene-1,4-diones and 2-en-1-ones with di-i-butylaluminium hydride
inferredcites →https://doi.org/10.1063/1.1139043openalex-snapshot
Low-cost, high-performance quadrupole mass spectrometer based on a low-performance rf generator
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.2020.112642zenodo-depositor-declared
Trinor- and tetranor-eremophilane sesquiterpenoids with anti-neuroinflammatory activity from cultures of the fungus Septoria rudbeckiae
inferred← citeshttps://doi.org/10.1002/9781118120392.ch4openalex-snapshot
Electronic CD Exciton Chirality Method: Principles and Applications
inferred← citeshttps://doi.org/10.1002/chin.198930288openalex-snapshot
ChemInform Abstract: Novel Trinor‐Eremophilanes (Dendryphiellin B, C, and D), Eremophilanes (Dendryphiellin E, F, and G), and Branched C9‐Carboxylic Acids (Dendryphiellic Acid A and B) from the Marine Deuteromycete Dendryphiella salina (Sutherland) Pugh et Nicot
inferred← citeshttps://doi.org/10.1002/ejoc.200700782openalex-snapshot
A Temporary Stereocentre Approach for the Stereodivergent Synthesis of Either Enantiomer of α‐Methyloctanal
inferred← citeshttps://doi.org/10.1002/hlca.19900730804openalex-snapshot
A novel glyceryl ester (glyceryl dendryphiellate A), a trinor‐eremophilane (dendryphiellin A1), and eremophilanes (dendryphiellin E1 and E2) from the marine deuteromycete Dendryphiella salina (S UTHERLAND ) P UGH et N ICOT
inferred← citeshttps://doi.org/10.1002/hlca.200890189openalex-snapshot
Triterpenoid Ester Saponins from Dipteronia dyeriana
inferred← citeshttps://doi.org/10.1002/prac.19983400702openalex-snapshot
Advances in chemical studies on low-molecular weight metabolites of marine fungi
inferred← citeshttps://doi.org/10.1007/978-1-4899-2391-2_12openalex-snapshot
Marine Microorganisms: A New Biomedical Resource
inferred← citeshttps://doi.org/10.1007/978-981-10-4768-8_5openalex-snapshot
Marine Filamentous Fungi: Diversity, Distribution and Bioprospecting
inferred← citeshttps://doi.org/10.1007/s11557-006-0504-yopenalex-snapshot
Physiological responses of marine Dendryphiella species from different geographical locations
inferred← citeshttps://doi.org/10.1007/s13225-011-0119-8openalex-snapshot
Fifty years of marine mycology
inferred← citeshttps://doi.org/10.1007/s13225-016-0358-9openalex-snapshot
Mycochemistry of marine algicolous fungi
inferred← citeshttps://doi.org/10.1016/0031-9422(91)84187-wopenalex-snapshot
A phytotoxic eremophilane ether from Hypomyces odoratus
inferred← citeshttps://doi.org/10.1016/b978-0-444-63931-8.00007-2openalex-snapshot
Nonhalogenated Heterotricyclic Sesquiterpenes From Marine Origin I
inferred← citeshttps://doi.org/10.1016/b978-0-444-89558-5.50031-6openalex-snapshot
Extended Conjugate Addition Reactions: The Synthesis and Nucleophilic Addition Chemistry of Polyunsaturated Carbonyl Compounds
inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00188-xopenalex-snapshot
Characterization by Circular Dichroism Spectroscopy
inferred← citeshttps://doi.org/10.1016/j.fitote.2013.08.023openalex-snapshot
Norbisabolane and eremophilane sesquiterpenoids from cultures of the Basidiomycete Polyporus ellisii
inferred← citeshttps://doi.org/10.1016/j.phytochem.2016.03.005openalex-snapshot
Eremophilane sesquiterpenes from Hawaiian endophytic fungus Chaetoconis sp. FT087
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133297openalex-snapshot
Eremophilane sesquiterpenoids from the endophytic fungus Curvularia lunata BCC76963
inferred← citeshttps://doi.org/10.1016/s0040-4020(99)00407-xopenalex-snapshot
Synthesis of dendryphiellin C, a trinor-sesquiterpene from a marine source
inferred← citeshttps://doi.org/10.1016/s0065-2164(08)70223-5openalex-snapshot
Marine Microorganisms as a Source of New Natural Products
inferred← citeshttps://doi.org/10.1016/s1572-5995(00)80059-9openalex-snapshot
Marine Fungal Substances
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00528openalex-snapshot
Nematicidal Stemona Alkaloids from Stemona parviflora
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00015openalex-snapshot
Cytotoxic and Antibacterial Eremophilane Sesquiterpenes from the Marine-Derived Fungus Cochliobolus lunatus SCSIO41401
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01765openalex-snapshot
Synthetic Preparation of the Macrocyclolipopeptide Dysoxylactam A for Potent P-glycoprotein Inhibition
inferred← citeshttps://doi.org/10.1021/ja981540nopenalex-snapshot
Ruthenium-Catalyzed Alder Ene Type Reactions. A Formal Synthesis of Alternaric Acid
inferred← citeshttps://doi.org/10.1021/np1000889openalex-snapshot
Cryptosphaerolide, a Cytotoxic Mcl-1 Inhibitor from a Marine-Derived Ascomycete Related to the Genus Cryptosphaeria
inferred← citeshttps://doi.org/10.1039/b301926hopenalex-snapshot
Marine-derived fungi: a chemically and biologically diverse group of microorganisms
inferred← citeshttps://doi.org/10.1039/c9ra08119dopenalex-snapshot
Marine unsaturated fatty acids: structures, bioactivities, biosynthesis and benefits
inferred← citeshttps://doi.org/10.1080/10575639908045430openalex-snapshot
An Eremophylane-Type Sesquiterpene and Diterpenes from Roots ofSalvia Mellifera
inferred← citeshttps://doi.org/10.1080/14786419.2017.1309535openalex-snapshot
Two new phenolic constituents from the root bark of Morus alba L. and their cardioprotective activity
inferred← citeshttps://doi.org/10.1080/21501203.2014.931308openalex-snapshot
An assessment of natural product discovery from marine ( sensu strictu ) and marine-derived fungi
inferred← citeshttps://doi.org/10.1177/1934578x221109527openalex-snapshot
Cumulative Data of 1 H and 13 C NMR Signals and Specific Rotations of Eremophilane Sesquiterpenoids. 1. Bicyclic Eremophilanes (1)
inferred← citeshttps://doi.org/10.1177/1934578x221141172openalex-snapshot
Cumulative Data of 1 H and 13 C NMR Signals and Specific Rotations of Eremophilane Sesquiterpenoids. 2. Bicyclic Eremophilanes (2)
inferred← citeshttps://doi.org/10.1201/b19081-16openalex-snapshot
Bioprospecting Fungi and the Labyrinthulomycetes at the Ocean–Land Interface
inferred← citeshttps://doi.org/10.1515/bot-2015-0013openalex-snapshot
Secondary metabolites of the marine fungus Paradendryphiella arenariae BCC 17999
inferred← citeshttps://doi.org/10.1515/bot-2023-0015openalex-snapshot
Recent progress in marine mycological research in different countries, and prospects for future developments worldwide
inferred← citeshttps://doi.org/10.1515/bot-2023-0017openalex-snapshot
History of marine mycology – a personal perspective
inferred← citeshttps://doi.org/10.1515/bot.2008.028openalex-snapshot
Marine endophyte sources of new chemical natural products: a review
inferred← citeshttps://doi.org/10.1515/bot.2008.029openalex-snapshot
Screening strategies for obtaining novel, biologically active, fungal secondary metabolites from marine habitats
inferred← citeshttps://doi.org/10.1515/bot.2008.030openalex-snapshot
Review of bioactive compounds from fungi in the South China Sea
inferred← citeshttps://doi.org/10.3390/md18040191openalex-snapshot
Secondary Metabolites from the Culture of the Marine-derived Fungus Paradendryphiella salina PC 362H and Evaluation of the Anticancer Activity of Its Metabolite Hyalodendrin
inferred← citeshttps://doi.org/10.3390/plants11060769openalex-snapshot
Structures, Occurrences and Biosynthesis of 11,12,13-Tri-nor-Sesquiterpenes, an Intriguing Class of Bioactive Metabolites
inferred← citeshttps://doi.org/10.70675/370bd4faz60f7z4872z8de8z81868f186216openalex-snapshot
Caractérisation de molécules issues de microorganismes associés aux organismes marins, capables d'agir sur les cellules métastatiques du cancer du sein
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.