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Three New Furan Derivatives and a New Fatty Acid from a Taiwanese Marine Sponge Plakortis simplex
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf01193220openalex-snapshot
Furan fatty acids in butter and butter oil
inferredcites →https://doi.org/10.1007/bf01922995openalex-snapshot
A new furanoid fatty acid from the soft coralsSarcophyton glaucum andgemmatum
inferredcites →https://doi.org/10.1007/bf02535166openalex-snapshot
The common occurrence of furan fatty acids in plants
inferredcites →https://doi.org/10.1007/bf02535671openalex-snapshot
The composition of furan fatty acids in the crayfish
inferredcites →https://doi.org/10.1016/0040-4020(58)88007-2openalex-snapshot
Volatile constituents of black-rotted sweet potato and related substances
inferredcites →https://doi.org/10.1021/ja00830a030openalex-snapshot
Sulfur dioxide trapping of photochemically generated 1,4-biradicals
inferredcites →https://doi.org/10.1021/jo00372a030openalex-snapshot
Structure determination of oligomycins A and C
inferredcites →https://doi.org/10.1021/np50070a021openalex-snapshot
Peroxy Aliphatic Esters from the Sponge Plakortis lita
inferredcites →https://doi.org/10.1021/np50113a014openalex-snapshot
Isolation of the Furan Fatty Acid, (8Z,11Z,14Z,17Z)-3,6-Epoxyeicos-3,5,8,11,14,17-hexenoic Acid from the New Zealand Sponge Hymeniacidon hauraki
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a122356openalex-snapshot
Studies on Furan Fatty Acids of Salmon Roe Phospholipids
inferredcites →https://doi.org/10.1248/cpb.32.3281openalex-snapshot
Studies on lipids of crayfish, Procambarus clarkii. I. Furanoid fatty acids.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4466.1.4zenodo-depositor-declared
New sciaphilic plakinids (Porifera, Homoscleromorpha) from the Central-Western Pacific
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod019openalex-snapshot
Porifera (Sponges)–1
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod195openalex-snapshot
Porifera (Sponges)–5
inferred← citeshttps://doi.org/10.1002/ange.202015232openalex-snapshot
Unified Approach to Furan Natural Products via Phosphine‐Palladium Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202015232openalex-snapshot
Unified Approach to Furan Natural Products via Phosphine‐Palladium Catalysis
inferred← citeshttps://doi.org/10.1002/chem.200902023openalex-snapshot
Efficient Homogeneous Radical‐Anion Chain Reactions Initiated by Dissociative Electron Transfer to 3,3,6,6‐Tetraaryl‐1,2‐dioxanes
inferred← citeshttps://doi.org/10.1002/jccs.200600116openalex-snapshot
A Convenient Access to Functionalized Pyrazole, Pyrazolyl‐Azole, and Pyrazolo[3,4‐d]Pyridazine Derivatives
inferred← citeshttps://doi.org/10.1007/s10593-023-03224-9openalex-snapshot
Synthesis of 2-hexyl-5-ethylfuran-3-sulfonic acid (HEFS) – natural antithrombosis agent from Eisenia earthworms
inferred← citeshttps://doi.org/10.1007/s11745-003-1192-8openalex-snapshot
Synthesis of novel tri‐ and tetrasubstituted C18 furan fatty esters
inferred← citeshttps://doi.org/10.1007/s11745-012-3653-6openalex-snapshot
Absorption and Metabolism of cis‐9,trans‐11‐CLA and of Its Oxidation Product 9,11‐Furan Fatty Acid by Caco‐2 Cells
inferred← citeshttps://doi.org/10.1016/j.bse.2004.12.007openalex-snapshot
A survey for biochemical synapomorphies to reveal phylogenetic relationships of halichondrid demosponges (Metazoa: Porifera)
inferred← citeshttps://doi.org/10.1016/j.ejca.2004.09.005openalex-snapshot
Marine pharmacology in 2001–2: antitumour and cytotoxic compounds
inferred← citeshttps://doi.org/10.1016/j.ejmech.2007.04.019openalex-snapshot
Bioactive peroxides as potential therapeutic agents
inferred← citeshttps://doi.org/10.1016/j.phytochem.2008.10.007openalex-snapshot
Metabolites from the endophytic mitosporic Dothideomycete sp. LRUB20
inferred← citeshttps://doi.org/10.1016/j.plipres.2017.10.002openalex-snapshot
Furan fatty acids – Beneficial or harmful to health?
inferred← citeshttps://doi.org/10.1016/j.tet.2006.08.075openalex-snapshot
Chemical predisposition in synthesis: application to the preparation of the pyrrolidine natural products, plakoridines A and B
inferred← citeshttps://doi.org/10.1016/j.tet.2007.08.046openalex-snapshot
Recent advances in the chemistry of 2-(2-oxoalkylidene)tetrahydrofurans
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130751openalex-snapshot
Visible-light photoredox catalyzed synthesis of polysubstituted furfuryl trifluoroacetamide derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.02.124openalex-snapshot
A synthetic approach to the plakoridines modeled on a biogenetic theory
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.11.120openalex-snapshot
A general route to 5-substituted-2-furylacetic acids: a brief synthesis of plakorsin B
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.03.033openalex-snapshot
Thermally-induced ring contraction as a novel and straightforward route for the synthesis of 2-furyl acetonitrile derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.04.070openalex-snapshot
CuBr-catalyzed cascade reaction of 2-substituted-3-(1-alkynyl)chromones to synthesize functionalized 3-acylfurans
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)01984-0openalex-snapshot
New acetylenic furan derivatives: synthesis and anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)02879-4openalex-snapshot
Palladium(II) chloride catalyzes the cross-coupling reaction of 2,5-bis-(butyltelluro)-furan and 1-alkynes
inferred← citeshttps://doi.org/10.1016/s0959-6380(02)80009-5openalex-snapshot
Chapter 5.3 Five-membered ring systems: Furans and benzofurans
inferred← citeshttps://doi.org/10.1021/np070605+openalex-snapshot
Furan Metabolites from the Sponge-Derived Yeast Pichia membranifaciens
inferred← citeshttps://doi.org/10.1021/np300771popenalex-snapshot
Cytotoxic Polyketide Derivatives from the South China Sea Sponge Plakortis simplex
inferred← citeshttps://doi.org/10.1021/np900310jopenalex-snapshot
Aromatic Cyclic Peroxides and Related Keto-Compounds from the Plakortis sp. Component of a Sponge Consortium
inferred← citeshttps://doi.org/10.1039/b110829hopenalex-snapshot
Exploitation of chemical predisposition in synthesis: an approach to the manzamenones
inferred← citeshttps://doi.org/10.1039/b301909hopenalex-snapshot
Radical anion chain process initiated by a dissociative electron transfer to a monocyclic endoperoxide.
inferred← citeshttps://doi.org/10.1039/c0ob00695eopenalex-snapshot
Site-selective Suzuki–Miyaura cross-coupling reactions of 2,3,4,5-tetrabromofuran
inferred← citeshttps://doi.org/10.1039/c5np00142kopenalex-snapshot
Structural diversity and chemical synthesis of peroxide and peroxide-derived polyketide metabolites from marine sponges
inferred← citeshttps://doi.org/10.3184/0308234043431357openalex-snapshot
Synthesis of some new pyridazine, 1,2,4-triazine and 1,3,4-thiadiazole derivatives
inferred← citeshttps://doi.org/10.3390/ijms24043997openalex-snapshot
Bio-Derived Furanic Compounds with Natural Metabolism: New Sustainable Possibilities for Selective Organic Synthesis
inferred← citeshttps://doi.org/10.3390/md11114407openalex-snapshot
New Constituents from the Korean Sponge Plakortis simplex
inferred← citeshttps://doi.org/10.3390/md13095579openalex-snapshot
New Furan and Cyclopentenone Derivatives from the Sponge-Associated Fungus Hypocrea Koningii PF04
inferred← citeshttps://doi.org/10.3923/jpt.2013.1.18openalex-snapshot
Probing the Mechanism of Cytotoxic Furan 2-YL Acetate Using in vitro and in silico Analysis-pharmacological Study
inferred← citeshttps://doi.org/10.3987/rev-04-sr(p)1openalex-snapshot
Metabolites from Marine Sponges of the Genus Plakortis
inferred← citeshttps://doi.org/10.4172/2329-6836.1000336openalex-snapshot
(2S*,5S*,6Z)-2,5-Epoxydocosan-6-en-21-ynoic Acid, New Fatty Acid from the Marine Sponge Haliclona fascigera
inferred← citeshttps://doi.org/10.6023/a26050154openalex-snapshot
Advances in the Application of Mizoroki-Heck Reaction in Natural Product Synthesis ★
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