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Novel Polyketide Metabolites from a Species of Marine Fungi
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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.19760590306openalex-snapshot
Synthese des (R)‐trans‐11‐Hydroxy‐8‐dodecensäure‐lactons (Recieifeiolid)
inferredcites →https://doi.org/10.1002/hlca.19760590307openalex-snapshot
One‐Step Purification of Bovine Adrenal Glucose‐6‐phosphate Dehydrogenase by Affinity Chromatography
inferredcites →https://doi.org/10.1016/0031-9422(95)00414-3openalex-snapshot
Twelve-membered lactones produced by cladosporium tenuissimum and the plant growth retardant activity of cladospolide B
inferredcites →https://doi.org/10.1039/np9971400453openalex-snapshot
Secondary metabolites from marine microorganisms: bacteria, protozoa, algae and fungi. Achievements and prospects
inferredcites →https://doi.org/10.1139/v71-330openalex-snapshot
11-Hydroxy-trans-8-dodecenoic Acid Lactone, a 12-Membered-Ring Compound from a Fungus
inferredcites →https://doi.org/10.1246/bcsj.58.2147openalex-snapshot
Absolute Stereostructure Determination of Cladospolide A Using MTPA Ester Method
inferredcites →https://doi.org/10.7164/antibiotics.39.629openalex-snapshot
New macrolides from Penicillium urticae mutant S11R59.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Thiocladospolides F-J, antibacterial sulfur containing 12-membered macrolides from the mangrove endophytic fungus Cladosporium oxysporum HDN13-314
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Porifera (Sponges)–3
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Porifera (Sponges)–5
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A Unified Synthetic Strategy for Dendrodolides E, F, G, I, J, and L
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The Direct Asymmetric Vinylogous Aldol Reaction of Furanones with α‐Ketoesters: Access to Chiral γ‐Butenolides and Glycerol Derivatives
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The Direct Asymmetric Vinylogous Aldol Reaction of Furanones with α‐Ketoesters: Access to Chiral γ‐Butenolides and Glycerol Derivatives
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Two New Butenolides Produced by an Actinomycete Streptomyces sp.
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Chemical Constituents of the Deep‐Sea‐Derived Fungus Cladosporium oxysporum 170103 and Their Antibacterial Effects
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Asymmetric Total Synthesis of (−)‐Cladospolide B
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Alkyne‐Mediated Approach for Total Syntheses of Cladospolides A, B, C and iso‐Cladospolide B
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First Total Synthesis of the Proposed Structure of Pandangolide 1
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Three New Polyketide Metabolites from the Endophytic Fungal Strain Cladosporium tenuissimum LR463 of Maytenus hookeri
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Surprising Formation of Chlorinated Butenolides from Dialkyl Acetylenedicarboxylates and Hexachloroacetone in the Presence of Triphenyl Phosphite
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Stereoselective Total Synthesis of Iso‐Cladospolide B and the 12 Membered‐Macrolactone (6S,12R)‐6‐Hydroxy‐12‐methyloxacyclododecane‐2,5‐dione
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Harnessing Molecular and Bioactivity Network Analysis to Prioritize Antibacterial Compound Isolation From Ant‐Associated Fungi
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Bioactivity‐Guided Isolation, Antimicrobial and Cytotoxic Evaluation of Secondary Metabolites from Cladosporium tenuissimum Associated with Pinus wallichiana
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Secondary Metabolites from Higher Fungi: Discovery, Bioactivity, and Bioproduction
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Chemical Evolution of Indonesian Marine Natural Products
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Marine Natural Products from Marine Sponge Microorganisms
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Silica sulfuric acid as a reusable heterogeneous catalyst for the diastereoselective Mukaiyama aldol reaction of 2-(trimethylsilyloxy)furan: facile synthesis of γ-butenolides
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Chemical constituents of the roots of Pottsia laxiflora
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Bioactive products from Okinawan marine micro- and macroorganisms
inferred← citeshttps://doi.org/10.1007/s11274-008-9904-2openalex-snapshot
Antifouling and antibacterial compounds from a marine fungus Cladosporium sp. F14
inferred← citeshttps://doi.org/10.1007/s11274-023-03830-xopenalex-snapshot
Endophytic fungi of Lycium barbarum: isolation, determination, bioactivity and separation of compounds
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Fungal symbionts of marine sponges from Rameswaram, southern India: species composition and bioactive metabolites
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The intriguing chemistry and biology of sulfur-containing natural products from marine microorganisms (1987–2020)
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The Chemistry and Bioactivity of Macrolides from Marine Microorganisms
inferred← citeshttps://doi.org/10.1016/j.bmc.2020.115883openalex-snapshot
Polyketides from the marine-derived fungus Aspergillus falconensis: In silico and in vitro cytotoxicity studies
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.06.072openalex-snapshot
Lipid-lowering polyketides from a soft coral-derived fungus Cladosporium sp. TZP29
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Efficient synthesis of functionalized butenolides mediated by vinyltriphenylphosphonium salts in aqueous media
inferred← citeshttps://doi.org/10.1016/j.cdc.2023.101000openalex-snapshot
Total synthesis of the proposed structure of Pandangolide 1
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Thiocladospolide E and cladospamide A, novel 12-membered macrolide and macrolide lactam from mangrove endophytic fungus Cladosporium sp. SCNU-F0001
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A novel property of propolis (bee glue): Anti-pathogenic activity by inhibition of N-acyl-homoserine lactone mediated signaling in bacteria
inferred← citeshttps://doi.org/10.1016/j.phytochem.2007.01.020openalex-snapshot
Secondary metabolite chemistry of the marine-derived fungus Massarina sp., strain CNT-016
inferred← citeshttps://doi.org/10.1016/j.tet.2006.12.015openalex-snapshot
Application of hydrolytic kinetic resolution (HKR) in the synthesis of bioactive compounds
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Synthesis and stereochemical assignment of (+)-Cladospolide D
inferred← citeshttps://doi.org/10.1016/j.tet.2014.06.025openalex-snapshot
Protecting group-free syntheses of natural products and biologically active compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2016.06.042openalex-snapshot
Total synthesis, biological evaluation of dendrodolides A–D and their analogues
inferred← citeshttps://doi.org/10.1016/j.tet.2019.04.001openalex-snapshot
Formal synthesis of Cladospolide C & epi-Cladospolide C using R-(+)-γ-valerolactone as a chiral synthon
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.01.011openalex-snapshot
Facile enantiospecific synthesis of (+)-iso-cladospolide B
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.02.018openalex-snapshot
Enantioselective total synthesis of iso-cladospolide B, cladospolide C and cladospolide B from tartaric acid
inferred← citeshttps://doi.org/10.1016/j.tetasy.2016.01.013openalex-snapshot
Total synthesis of (+)-cladospolide D
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.07.153openalex-snapshot
Efficient total synthesis of iso-cladospolide B and cladospolide B
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.07.043openalex-snapshot
Attempts directed towards the synthesis and determination of the absolute stereochemistry of iso-cladospolide-B and cladospolides-B and C
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.07.044openalex-snapshot
First synthesis and determination of the absolute stereochemistry of iso-cladospolide-B and cladospolides-B and C
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.09.143openalex-snapshot
The first organocatalytic addition of 2-trimethylsilyloxyfuran to carbonyl compounds: hydrogen-bond catalysis in γ-butenolides synthesis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.09.145openalex-snapshot
The first total synthesis of sporiolide B
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.08.123openalex-snapshot
Synthesis of butenolides recently isolated from marine microorganisms
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An efficient total synthesis of (+)-Cladospolide C
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.04.124openalex-snapshot
Synthesis of (4S, 5S, 11R) and (4S, 5S, 11S)-iso-cladospolide B
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.11.044openalex-snapshot
The first stereoselective synthesis of dendrodolide A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.04.097openalex-snapshot
A short and concise route to total synthesis of Dendrodolide L
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)00323-9openalex-snapshot
Synthesis and structure determination of iso -cladospolide B
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)02602-3openalex-snapshot
A novel and simple method to prepare γ-hydroxy-α,β-(E)-alkenoic esters from γ-keto-alkynoic esters
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Synthesis of furanone-Based natural product analogues with quorum sensing antagonist activity
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Isolation and molecular characterization of bioactive secondary metabolites from Callyspongia spp. associated fungi
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00791openalex-snapshot
Berkeleylactones and a Citreohybriddione Analogue from Penicillium turbatum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00295openalex-snapshot
Condensation of Macrocyclic Polyketides Produced byPenicilliumsp. DRF2 with Mercaptopyruvate Represents a New Fungal Detoxification Pathway
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The Berkeleylactones, Antibiotic Macrolides from Fungal Coculture
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Thiocladospolides A–D, 12-Membered Macrolides from the Mangrove-Derived Endophytic Fungus Cladosporium cladosporioides MA-299 and Structure Revision of Pandangolide 3
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Catalyst-Controlled Regioselective Nitrosocarbonyl Aldol Reaction of Deconjugated Butenolides
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Chiral Spirophosphoric-Acid-Catalyzed Divergent Vinylogous Mannich and aza-Friedel–Crafts Reactions of 2-Methoxyfuran
inferred← citeshttps://doi.org/10.1021/ja0578348openalex-snapshot
Palladium-Catalyzed Asymmetric Allylic Alkylation of meso- and dl-1,2-Divinylethylene Carbonate
inferred← citeshttps://doi.org/10.1021/jm030090topenalex-snapshot
Structures and Cytotoxic Properties of Trichoverroids and Their Macrolide Analogues Produced by Saltwater Culture of Myrothecium verrucaria
inferred← citeshttps://doi.org/10.1021/jo0615504openalex-snapshot
The First Total Synthesis of Sporiolide A
inferred← citeshttps://doi.org/10.1021/jo400861jopenalex-snapshot
Structure, Absolute Configuration, and Conformational Study of 12-Membered Macrolides from the Fungus Dendrodochium sp. Associated with the Sea Cucumber Holothuria nobilis Selenka
inferred← citeshttps://doi.org/10.1021/np0001676openalex-snapshot
New Butenolides from Two Marine Streptomycetes
inferred← citeshttps://doi.org/10.1021/np000401sopenalex-snapshot
New Macrolides and Furan Carboxylic Acid Derivative from the Sponge-Derived Fungus Cladosporium herbarum
inferred← citeshttps://doi.org/10.1021/np020196bopenalex-snapshot
Novel Chromone Derivatives from the Fungus Aspergillus versicolor Isolated from the Marine Sponge Xestospongia exigua
inferred← citeshttps://doi.org/10.1021/np030388mopenalex-snapshot
Expanding the Strategies in Natural Product Studies of Marine-Derived Fungi: A Chemical Investigation of Penicillium Obtained from Deep Water Sediment
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Dictyosphaeric Acids A and B: New Decalactones from an Undescribed Penicillium sp. Obtained from the Alga Dictyosphaeria versluyii
inferred← citeshttps://doi.org/10.1021/np0501583openalex-snapshot
Pandangolide 1a, a Metabolite of the Sponge-Associated Fungus Cladosporium sp., and the Absolute Stereochemistry of Pandangolide 1 and iso-Cladospolide B
inferred← citeshttps://doi.org/10.1021/np070610dopenalex-snapshot
Botryolides A−E, Decarestrictine Analogues from a Fungicolous Botryotrichum sp. (NRRL 38180)
inferred← citeshttps://doi.org/10.1021/ol0495366openalex-snapshot
Trans-Selective Conversions of γ-Hydroxy-α,β-Alkynoic Esters to γ-Hydroxy-α,β-Alkenoic Esters
inferred← citeshttps://doi.org/10.1021/ol102599eopenalex-snapshot
Stereoselective Synthesis and Structural Correction of the Naturally Occurring Lactone Stagonolide G
inferred← citeshttps://doi.org/10.1021/ol703065xopenalex-snapshot
C1-Symmetric Oxazolinyl Sulfoximines as Ligands in Copper-Catalyzed Asymmetric Mukaiyama Aldol Reactions
inferred← citeshttps://doi.org/10.1021/ol9000119openalex-snapshot
De Novo Asymmetric Synthesis of Cladospolide B−D: Structural Reassignment of Cladospolide D via the Synthesis of its Enantiomer
inferred← citeshttps://doi.org/10.1038/s42255-023-00830-xopenalex-snapshot
Improved polyketide production in C. glutamicum by preventing propionate-induced growth inhibition
inferred← citeshttps://doi.org/10.1039/b110018aopenalex-snapshot
A chemoenzymatic synthesis of the 12-membered macrolide (–)-cladospolide A
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/b401829jopenalex-snapshot
A chemoenzymatic total synthesis of the phytotoxic undecenolide (−)-cladospolide A
inferred← citeshttps://doi.org/10.1039/b417685eopenalex-snapshot
A chemoenzymatic total synthesis of the undecenolide (−)-cladospolide B via a mid-stage ring-closing metathesis and a late-stage photo-rearrangement of the E-isomer
inferred← citeshttps://doi.org/10.1039/b923925aopenalex-snapshot
Efficient direct asymmetric vinylogous Michael addition reactions of γ-butenolides to chalcones catalyzed by vicinal primary-diamine salts
inferred← citeshttps://doi.org/10.1039/c0cc02352copenalex-snapshot
Pd-catalyzed 5- endo-trig -type cyclization of β,γ-unsaturated carbonyl compounds: an efficient ring closing reaction to give γ-butenolides and 3-pyrrolin-2-ones
inferred← citeshttps://doi.org/10.1039/c1ob05787aopenalex-snapshot
A flexible and unified strategy for syntheses of cladospolides A, B, C, and iso-cladospolide B
inferred← citeshttps://doi.org/10.1039/c9ra08119dopenalex-snapshot
Marine unsaturated fatty acids: structures, bioactivities, biosynthesis and benefits
inferred← citeshttps://doi.org/10.1039/d2qo00321jopenalex-snapshot
Synthesis of γ-hydroxy-γ-perfluoroalkyl butenolides and exocyclic double bond butanolides via regioselective allylic alkylations of MBH carbonates with 2-perfluoroalkyl-oxazol-5(2 H )-ones
inferred← citeshttps://doi.org/10.1071/ch05074openalex-snapshot
A Chemoenzymatic Total Synthesis of the Undecenolide (-)-Cladospolide C
inferred← citeshttps://doi.org/10.1080/00397911.2019.1639757openalex-snapshot
Total synthesis of pandangolide 1 proposed structure
inferred← citeshttps://doi.org/10.1080/00397911.2019.1692356openalex-snapshot
First total synthesis of 5( S )-hydroxyrecifeiolide
inferred← citeshttps://doi.org/10.1080/00397911.2023.2220443openalex-snapshot
An alternate synthesis of sporiolide B from ( R )-glyceraldehyde
inferred← citeshttps://doi.org/10.1080/10286020.2013.817389openalex-snapshot
Polyketides from the plant endophytic fungusCladosporiumsp. IFB3lp-2
inferred← citeshttps://doi.org/10.1080/10286020.2018.1471067openalex-snapshot
Two new 12-membered macrolides from the endophytic fungal strain Cladosprium colocasiae A801 of Callistemon viminalis
inferred← citeshttps://doi.org/10.1080/14786410500137718openalex-snapshot
Phenylalkylamine alkaloids fromStapelia hirsuta L.
inferred← citeshttps://doi.org/10.1080/14786419.2019.1608543openalex-snapshot
Alternative total synthesis of dendrodolide-L
inferred← citeshttps://doi.org/10.1111/cbdd.12783openalex-snapshot
Twelve‐membered macrolactones: privileged scaffolds for the development of new therapeutics
inferred← citeshttps://doi.org/10.1201/b19224-18openalex-snapshot
Secondary metabolites from microorganisms isolated from marine sponges from 2000 to 2012
inferred← citeshttps://doi.org/10.1201/b19224-19openalex-snapshot
Broad spectrum antimicrobial compounds from plants and rhizosphere microorganisms
inferred← citeshttps://doi.org/10.26686/wgtn.17138681openalex-snapshot
Revisiting marine bioprospecting of tropical Indonesian macroalgae from West Timor
inferred← citeshttps://doi.org/10.26686/wgtn.17138681.v1openalex-snapshot
Revisiting marine bioprospecting of tropical Indonesian macroalgae from West Timor
inferred← citeshttps://doi.org/10.3390/books978-3-0365-2753-6openalex-snapshot
Bioactive Marine Heterocyclic Compounds
inferred← citeshttps://doi.org/10.3390/ddc4010006openalex-snapshot
Antimicrobial and Anticancer Potential of Polyketides Isolated from the Caribbean Marine Sponge Plakortis halichondrioides
inferred← citeshttps://doi.org/10.3390/md13074171openalex-snapshot
Bioactive 7-Oxabicyclic[6.3.0]lactam and 12-Membered Macrolides from a Gorgonian-Derived Cladosporium sp. Fungus
inferred← citeshttps://doi.org/10.3390/md17050296openalex-snapshot
Polyketides from the Mangrove-Derived Endophytic Fungus Cladosporium cladosporioides
inferred← citeshttps://doi.org/10.3390/md17060364openalex-snapshot
Marine Natural Products from Indonesian Waters
inferred← citeshttps://doi.org/10.3390/md19040180openalex-snapshot
Marine-Derived Macrolides 1990–2020: An Overview of Chemical and Biological Diversity
inferred← citeshttps://doi.org/10.3390/md20080028openalex-snapshot
A Tropical Marine Microbial Natural Products Geobibliography as an Example of Desktop Exploration of Current Research Using Web Visualisation Tools
inferred← citeshttps://doi.org/10.3390/md20120765openalex-snapshot
Sulfur-Containing Metabolites from Marine and Terrestrial Fungal Sources: Origin, Structures, and Bioactivities
inferred← citeshttps://doi.org/10.3390/md204164openalex-snapshot
Sporiolides A and B, New Cytotoxic Twelve-Membered Macrolides from a Marine-Derived Fungus Cladosporium Species
inferred← citeshttps://doi.org/10.3390/molecules14072594openalex-snapshot
Calixpyrrole Derivatives: “Multi Hydrogen Bond” Catalysts for γ-Butenolide Synthesis
inferred← citeshttps://doi.org/10.3390/molecules25040853openalex-snapshot
Biological and Chemical Diversity of Marine Sponge-Derived Microorganisms over the Last Two Decades from 1998 to 2017
inferred← citeshttps://doi.org/10.3390/molecules26133959openalex-snapshot
The Genus Cladosporium: A Rich Source of Diverse and Bioactive Natural Compounds
inferred← citeshttps://doi.org/10.3390/org5020003openalex-snapshot
Supramolecular Catalysis with Chiral Mono- and Bis-(Thio)Urea-Derivatives
inferred← citeshttps://doi.org/10.3762/bjoc.15.34openalex-snapshot
Thiol-free chemoenzymatic synthesis of β-ketosulfides
inferred← citeshttps://doi.org/10.3987/com-06-10823openalex-snapshot
A Butenolide from the Marine Sponge Callyspongia vaginalis
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