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Three New Cyclic Peroxides from the Marine Sponge Plakortis aff 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/10.1002/hlca.19860690325openalex-snapshot
Cacospongione A, cacospongienone A, and cacospongienone B, new C21 difuran terpenoids from the marine sponge Cacospongiascalaris S CHMIDT of the Côte d' Azur
inferredcites →https://doi.org/10.1007/bf01407314openalex-snapshot
A simple screening procedure for the quantitative measurement of cytotoxicity to resting primary lymphocyte cultures
inferredcites →https://doi.org/10.1021/jo00023a048openalex-snapshot
Cytotoxic five-membered cyclic peroxides from a Plakortis sponge
inferredcites →https://doi.org/10.1021/np50112a006openalex-snapshot
New Cytotoxic Peroxylactones from the Marine Sponge, Plakinastrella onkodes
inferredcites →https://doi.org/10.1021/np970407qopenalex-snapshot
Two New C22 1,2-Dioxane Polyketides from the Marine Sponge Acarnus cf. bergquistae
inferredcites →https://doi.org/10.1093/jnci/82.13.1107openalex-snapshot
New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening
inferredcites →https://doi.org/10.1093/jnci/83.11.757openalex-snapshot
Feasibility of a High-Flux Anticancer Drug Screen Using a Diverse Panel of Cultured Human Tumor Cell Lines
inferredcites →https://doi.org/10.1093/jnci/83.11.766openalex-snapshot
Effects of a Low-Fat Diet on Levels of Oxidative Damage to DNA in Human Peripheral Nucleated Blood Cells
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.4178.2.3zenodo-depositor-declared
Sponge epizoism in the Caribbean and the discovery of new Plakortis and Haliclona species, and polymorphism of Xestospongia deweerdtae (Porifera)
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/ejoc.202000980openalex-snapshot
Synthesis of 3,5‐Disubstituted 1,2‐Dioxolanes
inferred← citeshttps://doi.org/10.1007/978-81-322-2794-6_10openalex-snapshot
Bioactive Potential of Sponge Secondary Metabolites
inferred← citeshttps://doi.org/10.1007/978-81-322-2794-6_11openalex-snapshot
Typification of Chemical Compounds of Marine Sponge Metabolites
inferred← citeshttps://doi.org/10.1016/bs.aihch.2021.03.001openalex-snapshot
Advances in the synthesis of 1,2-dioxolanes and 1,2-dioxanes
inferred← citeshttps://doi.org/10.1016/j.ejca.2006.05.019openalex-snapshot
Marine pharmacology in 2003–2004: Anti-tumour 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.tet.2006.01.110openalex-snapshot
The power of singlet oxygen chemistry in biomimetic syntheses
inferred← citeshttps://doi.org/10.1016/j.tet.2009.11.068openalex-snapshot
Cyclisation of 1,2-dioxines containing tethered hydroxyl and carboxylic acid functionality: synthesis of tetrahydrofurans and dihydrofuran-2(3H)-ones
inferred← citeshttps://doi.org/10.1016/j.tet.2012.03.024openalex-snapshot
Exploratory studies toward the synthesis of the peroxylactone unit of plakortolides
inferred← citeshttps://doi.org/10.1016/j.tet.2012.04.025openalex-snapshot
Simplexolides A–E and plakorfuran A, six butyrate derived polyketides from the marine sponge Plakortis simplex
inferred← citeshttps://doi.org/10.1016/j.tet.2012.10.022openalex-snapshot
Asymmetric synthesis of andavadoic acid via base-catalyzed 5-exo-tet cyclization of a β-hydroperoxy epoxide
inferred← citeshttps://doi.org/10.1017/s0025315413000295openalex-snapshot
Five new species of Homoscleromorpha (Porifera) from the Caribbean Sea and re-description of Plakina jamaicensis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00951openalex-snapshot
Peroxide Natural Products from Plakortis zyggompha and the Sponge Association Plakortis halichondrioides–Xestospongia deweerdtae: Antifungal Activity against Cryptococcus gattii
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00056openalex-snapshot
Sc(OTf)3-Catalyzed C–C Bond-Forming Reaction of Cyclic Peroxy Ketals for the Synthesis of Highly Functionalized 1,2-Dioxene Endoperoxides
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01457openalex-snapshot
Synthesis of Plakortolides E and I Enabled by Base Metal Catalysis
inferred← citeshttps://doi.org/10.1021/jo8020659openalex-snapshot
A Short Access to 3-Hydroxy-4-hydroxymethyltetrahydrofurans: Application to the Total Synthesis of Amphiasterin B4
inferred← citeshttps://doi.org/10.1021/np100233dopenalex-snapshot
Chemical Constituents of the Deep Reef Caribbean Sponges Plakortis angulospiculatus and Plakortis halichondrioides and Their Anti-inflammatory Activities
inferred← citeshttps://doi.org/10.1021/np100461topenalex-snapshot
Bioactive Cycloperoxides Isolated from the Puerto Rican Sponge Plakortis halichondrioides
inferred← citeshttps://doi.org/10.1021/np100620xopenalex-snapshot
Configurational Assignment of Cyclic Peroxy Metabolites Provides an Insight into Their Biosynthesis: Isolation of Plakortolides, seco-Plakortolides, and Plakortones from the Australian Marine Sponge Plakinastrella clathrata
inferred← citeshttps://doi.org/10.1021/np3005634openalex-snapshot
Plakortolide Stereochemistry Revisited: The Checkered History of Plakortolides E and I
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/10.1021/ol203185fopenalex-snapshot
Total Synthesis of seco-Plakortolide E and (−)-ent-Plakortolide I: Absolute Configurational Revision of Natural Plakortolide I
inferred← citeshttps://doi.org/10.1038/s41598-019-38696-3openalex-snapshot
Aplysinopsin-type and Bromotyrosine-derived Alkaloids from the South China Sea Sponge Fascaplysinopsis reticulata
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/10.1039/c8np00011eopenalex-snapshot
Recent trends in the structural revision of natural products
inferred← citeshttps://doi.org/10.1039/d6ra00479bopenalex-snapshot
Cobalt catalysis in organic synthesis: a powerful tool in the synthesis of natural products and pharmaceutically active compounds
inferred← citeshttps://doi.org/10.1055/sos-sd-138-00094openalex-snapshot
38.8.3.2 Stable and Unstable 1,2-Dioxolanes: Origin, Synthesis, and Biological Activities
inferred← citeshttps://doi.org/10.1063/1.5127863openalex-snapshot
Interaction of oxygen with polystyrene and polyethylene polymer films: A mechanistic study
inferred← citeshttps://doi.org/10.3390/md11114407openalex-snapshot
New Constituents from the Korean Sponge Plakortis simplex
inferred← citeshttps://doi.org/10.3762/bjoc.10.6openalex-snapshot
Synthesis of five- and six-membered cyclic organic peroxides: Key transformations into peroxide ring-retaining products
inferred← citeshttps://doi.org/10.3987/com-11-12241openalex-snapshot
Synthesis of Peroxylactones Using Mn(III)-Catalyzed Aerobic Oxidation
inferred← citeshttps://doi.org/10.3987/rev-04-sr(p)1openalex-snapshot
Metabolites from Marine Sponges of the Genus Plakortis
inferred← citeshttps://doi.org/10.70675/6797e502z87aaz4438z85eez039ab1ede89bopenalex-snapshot
Metabolisme secondaire des éponges Homoscleromorpha : diversité et fluctuation de son expression en fonction des facteurs biotiques et abiotiques
inferred← citeshttps://doi.org/10.70675/892a61b4zb599z48c5z8ae8z29de20318e9fopenalex-snapshot
Synthetic studies toward plakortolides : asymmetric synthesis of ent-plakortolide I and seco-plakortolide E
inferred← citeshttps://doi.org/10.70675/af0e34c6z0519z498dz949ez405b22d4cc6eopenalex-snapshot
Synthèse et fonctionnalisation de 1,2-endoperoxydes 3,5-disubstitués, vers la synthèse totale de la mycangimycine.
inferred← citeshttps://doi.org/10.70675/e1f90413z5e0dz40c6zbd12zfb9360e627bbopenalex-snapshot
Recherche de molecules naturelles bioactives issues de la biodiversite marine de la zone sud-ouest de l'ocean Indien
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