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Structure, Absolute Configuration, and Conformational Study of 12-Membered Macrolides from the Fungus Dendrodochium sp. Associated with the Sea Cucumber Holothuria nobilis Selenka
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Assignment of the Absolute Configurations of Natural Products by Means of Solid‐State Electronic Circular Dichroism and Quantum Mechanical Calculations
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ECD cotton effect approximated by the Gaussian curve and other methods
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Absolute structural elucidation of natural products—A focus on quantum‐mechanical calculations of solid‐state CD spectra
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New Austalides from the Sponge‐Associated Fungus Aspergillus sp.
inferredcites →https://doi.org/10.1002/ejoc.201100675openalex-snapshot
Cytospolides A–E, New Nonanolides from an Endophytic Fungus, Cytospora sp.
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N–N‐Coupled Indolo‐sesquiterpene Atropo‐Diastereomers from a Marine‐Derived Actinomycete
inferredcites →https://doi.org/10.1002/ejoc.201201220openalex-snapshot
Alkaloids from the Sponge‐Associated Fungus Aspergillus sp.
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.200690055openalex-snapshot
Three New Polyketide Metabolites from the Endophytic Fungal Strain Cladosporium tenuissimum LR463 of Maytenus hookeri
inferredcites →https://doi.org/10.1002/hlca.201200064openalex-snapshot
A Convergent Synthesis of a Twelve‐Membered Macrolide Natural Product, (6R,12S)‐6‐Hydroxy‐12‐methyl‐1‐oxacyclododecane‐2,5‐dione
inferredcites →https://doi.org/10.1002/jcc.20495openalex-snapshot
Semiempirical GGA‐type density functional constructed with a long‐range dispersion correction
inferredcites →https://doi.org/10.1002/jlac.198819880104openalex-snapshot
Synthetic microbial chemistry, XVI. Synthesis of patulolides A, B, and C, new macrolides isolated from Penicillium urticae
inferredcites →https://doi.org/10.1002/jlac.1995199507185openalex-snapshot
A new synthesis of (±)‐phoracantholide, (±)‐dihydrorecifeiolide, and (±)‐muscone via α‐nitro ketones
inferredcites →https://doi.org/10.1007/s11274-008-9904-2openalex-snapshot
Antifouling and antibacterial compounds from a marine fungus Cladosporium sp. F14
inferredcites →https://doi.org/10.1016/0022-1759(83)90303-4openalex-snapshot
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
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/10.1016/j.tet.2008.10.059openalex-snapshot
Synthesis and stereochemical assignment of (+)-Cladospolide D
inferredcites →https://doi.org/10.1016/j.tetasy.2008.01.008openalex-snapshot
Total synthesis of patulolide C and 11-epipatulolide C
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.tetlet.2005.07.153openalex-snapshot
Efficient total synthesis of iso-cladospolide B and cladospolide B
inferredcites →https://doi.org/10.1016/j.tetlet.2006.07.026openalex-snapshot
A concise asymmetric route to the antibiotic macrolides patulolide A and pyrenophorin
inferredcites →https://doi.org/10.1016/j.tetlet.2006.09.145openalex-snapshot
The first total synthesis of sporiolide B
inferredcites →https://doi.org/10.1016/j.tetlet.2010.05.063openalex-snapshot
Enantioselective synthesis of (+)-patulolide C via proline-catalyzed sequential α-aminooxylation and Horner–Wadsworth–Emmons olefination
inferredcites →https://doi.org/10.1016/s0040-4020(01)85136-xopenalex-snapshot
Novel synthesis of 1,7-dihydrohept-4-yne derivatives: Application to the total synthesis of (±) patulolide A
inferredcites →https://doi.org/10.1016/s0040-4020(99)00164-7openalex-snapshot
Total synthesis of R-(+)-patulolide A and R-(−)-patulolide B: The macrolides isolated from Penicillium urticae mutant
inferredcites →https://doi.org/10.1016/s0040-4039(00)95093-7openalex-snapshot
Structure of patulolide a, a new macrolide from mutants
inferredcites →https://doi.org/10.1016/s0040-4039(01)93736-0openalex-snapshot
An enantioselective total synthesis of the macrolide Patulolide C
inferredcites →https://doi.org/10.1016/s0040-4039(98)02427-7openalex-snapshot
1,8-Stereocontrol by 1,5-induction using an allylstannane followed by Ireland-Claisen rearrangement: Diastereoselective total synthesis of (±)-patulolide C
inferredcites →https://doi.org/10.1016/s0960-894x(01)80868-4openalex-snapshot
Efficiency of non-ionic telomeric surfactants for the solubilization of subcellular fractions proteins
inferredcites →https://doi.org/10.1016/s0968-0896(00)82105-7openalex-snapshot
A synthesis of (R-recifeiolide by the aid of biochemical reaction as the key-step
inferredcites →https://doi.org/10.1021/ar960223nopenalex-snapshot
Configurational Assignment of Polyene Macrolide Antibiotics Using the [13C]Acetonide Analysis
inferredcites →https://doi.org/10.1021/cr000665jopenalex-snapshot
The Assignment of Absolute Configuration by NMR
inferredcites →https://doi.org/10.1021/ja00377a063openalex-snapshot
General method for determining absolute configuration of acyclic allylic alcohols
inferredcites →https://doi.org/10.1021/ja00417a033openalex-snapshot
A stereoselective synthesis of (+-)-11-hydroxy-trans-8-dodecenoic acid lactone, a naturally occurring macrolide from Cephalosporium recifei
inferredcites →https://doi.org/10.1021/jo00057a055openalex-snapshot
Synthesis of trans olefins by a nickel-catalyzed reduction of enol ethers. A formal, total synthesis of (.+-.)-recifeiolide
inferredcites →https://doi.org/10.1021/jo0264776openalex-snapshot
Ring Expansions of β-Keto Lactones with Zinc Carbenoids: Syntheses of (+)-Patulolide A and (±)-Patulolide B
inferredcites →https://doi.org/10.1021/jo201755vopenalex-snapshot
Bioactive Nonanolide Derivatives Isolated from the Endophytic FungusCytosporasp.
inferredcites →https://doi.org/10.1021/jo301592kopenalex-snapshot
Navigating the Fungal Polyketide Chemical Space: From Genes to Molecules
inferredcites →https://doi.org/10.1021/jo801944dopenalex-snapshot
Marinisporolides, Polyene-Polyol Macrolides from a Marine Actinomycete of the New Genus Marinispora
inferredcites →https://doi.org/10.1021/jo951339kopenalex-snapshot
Expedient Synthesis of (R)-Patulolide A
inferredcites →https://doi.org/10.1021/jo980942aopenalex-snapshot
Efficient Conditions for Conversion of 2-Substituted Furans into 4-Oxygenated 2-Enoic Acids and Its Application to Synthesis of (+)-Aspicilin, (+)-Patulolide A, and (−)-Pyrenophorin
inferredcites →https://doi.org/10.1021/np000401sopenalex-snapshot
New Macrolides and Furan Carboxylic Acid Derivative from the Sponge-Derived Fungus Cladosporium herbarum
inferredcites →https://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
inferredcites →https://doi.org/10.1021/np0504964openalex-snapshot
Chloriolide, a 12-Membered Macrolide from Chloridium virescens var. chlamydosporum (NRRL 37636)
inferredcites →https://doi.org/10.1021/np300642topenalex-snapshot
Herbarone, a Rearranged Heptaketide Derivative from the Sea Hare Associated Fungus Torula herbarum
inferredcites →https://doi.org/10.1021/np8003326openalex-snapshot
Ten-Membered Lactones from the Marine-Derived Fungus Curvularia sp.
inferredcites →https://doi.org/10.1021/np990361wopenalex-snapshot
Novel Polyketide Metabolites from a Species of Marine Fungi
inferredcites →https://doi.org/10.1021/ol005983jopenalex-snapshot
A New Approach to Macrocyclization via Alkene Formation in Catalytic Diazo Decomposition. Synthesis of Patulolides A and B
inferredcites →https://doi.org/10.1021/ol025540aopenalex-snapshot
Integramides A and B, Two Novel Non-Ribosomal Linear Peptides Containing Nine Cα-Methyl Amino Acids Produced by Fungal Fermentations That Are Inhibitors of HIV-1 Integrase
inferredcites →https://doi.org/10.1021/ol034944fopenalex-snapshot
Efficient Two-Step Conversion of α,β-Unsaturated Aldehydes to Optically Active γ-Oxy-α,β-unsaturated Nitriles and Its Application to the Total Synthesis of (+)-Patulolide C
inferredcites →https://doi.org/10.1021/ol2034299openalex-snapshot
Synthesis of (+)-Patulolide C via an Asymmetric Hydroformylation/Macrocyclization Cascade
inferredcites →https://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
inferredcites →https://doi.org/10.1038/nchembio.912openalex-snapshot
A fungal ketoreductase domain that displays substrate-dependent stereospecificity
inferredcites →https://doi.org/10.1039/b401829jopenalex-snapshot
A chemoenzymatic total synthesis of the phytotoxic undecenolide (−)-cladospolide A
inferredcites →https://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
inferredcites →https://doi.org/10.1039/b704420hopenalex-snapshot
Polyketides, proteins and genes in fungi: programmed nano-machines begin to reveal their secrets
inferredcites →https://doi.org/10.1039/c1ob05787aopenalex-snapshot
A flexible and unified strategy for syntheses of cladospolides A, B, C, and iso-cladospolide B
inferredcites →https://doi.org/10.1039/c2ob25992copenalex-snapshot
An approach to aliphatic 1,8-stereocontrol: diastereoselective syntheses of (±)-patulolide C and (±)-epipatulolide C
inferredcites →https://doi.org/10.1055/s-0029-1217107openalex-snapshot
Stereoselective Synthesis of (10S,12S)-10-Hydroxy-12-methyl-1-oxacyclododecane-2,5-dione via Prins Cyclization
inferredcites →https://doi.org/10.1055/s-0031-1290986openalex-snapshot
Protecting Group-Free Syntheses of (4S,5S,11R)- and (4S,5S,11S)-iso-Cladospolide B and Their Biological Evaluation
inferredcites →https://doi.org/10.1055/s-0031-1291154openalex-snapshot
Total Synthesis of (+)-Cladospolide A
inferredcites →https://doi.org/10.1055/s-1993-25820openalex-snapshot
Eine Synthese für (R)-(+)-Patulolid A
inferredcites →https://doi.org/10.1071/ch05074openalex-snapshot
A Chemoenzymatic Total Synthesis of the Undecenolide (-)-Cladospolide C
inferredcites →https://doi.org/10.1080/00397918608056359openalex-snapshot
A Short, Efficient and Stereos Elective Synthesis of (±)-Recifeiolide
inferredcites →https://doi.org/10.1080/00397918808068279openalex-snapshot
A Short Convergent Synthesis of (±) Patulolide A
inferredcites →https://doi.org/10.1080/00397919608003797openalex-snapshot
Synthesis of (±)-Recifeiolide and Its Homologs via Acetylenic Lactones
inferredcites →https://doi.org/10.1080/00397919908085781openalex-snapshot
The Synthesis of (±)-Patulolide C and its Epimer Via Dodec-3-En-11-Olide
inferredcites →https://doi.org/10.1107/s0108767383001762openalex-snapshot
On enantiomorph-polarity estimation
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/10.1248/cpb.40.1616openalex-snapshot
Synthesis of the Simple Macrolides, Patulolide A and Patulolide C.
inferredcites →https://doi.org/10.3390/md204164openalex-snapshot
Sporiolides A and B, New Cytotoxic Twelve-Membered Macrolides from a Marine-Derived Fungus Cladosporium Species
inferredcites →https://doi.org/10.3390/md9050844openalex-snapshot
Balticolid: A New 12-Membered Macrolide with Antiviral Activity from an Ascomycetous Fungus of Marine Origin
inferredcites →https://doi.org/10.3987/com-94-s(b)47openalex-snapshot
A Concise Enantiocontrolled Route to (+)-Patulolide C
inferredcites →https://doi.org/10.7164/antibiotics.39.629openalex-snapshot
New macrolides from Penicillium urticae mutant S11R59.
inferredcites →https://doi.org/10.7164/antibiotics.41.1649openalex-snapshot
Biosynthesis of the macrolide antibiotic patulolides by Penicillium urticae S11R59: Identification of the origin of carbon atoms by 13C NMR spectroscopy.
inferredcites →https://doi.org/10.7164/antibiotics.54.635openalex-snapshot
Cladospolide D, a New 12-Membered Macrolide Antibiotic Produced by Cladosporium sp. FT-0012.
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Cytotoxic 14-Membered Macrolides from a Mangrove-Derived Endophytic Fungus,Pestalotiopsis microspora
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00581openalex-snapshot
Phenanthrenes fromJuncus inflexuswith Antimicrobial Activity against Methicillin-ResistantStaphylococcus aureus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00809openalex-snapshot
Antibacterial and Cytotoxic Phenolic Metabolites from the Fruits ofAmorpha fruticosa
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00694openalex-snapshot
Chimeric Pyridone Alkaloids from the Mangrove Endophytic Fungus Aspergillus niger
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00463openalex-snapshot
Immunomodulatory Polyketides from a Phoma-like Fungus Isolated from a Soft Coral
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00191openalex-snapshot
Flabellipparicine, a Flabelliformide-Apparicine-Type Bisindole Alkaloid from Tabernaemontana divaricata
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00373openalex-snapshot
Chaetolines A and B, Pyrano[3,2- f ]isoquinoline Alkaloids from Cultivation of Chaetomium sp. in the Presence of Autoclaved Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00482openalex-snapshot
A Pair of Enantiomeric Bis-seco-abietane Diterpenoids fromCryptomeria fortunei
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00540openalex-snapshot
Azaphilone Derivatives from the Fungus Coniella fragariae Inhibit NF-κB Activation and Reduce Tumor Cell Migration
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b01091openalex-snapshot
Thiocladospolides A–D, 12-Membered Macrolides from the Mangrove-Derived Endophytic Fungus Cladosporium cladosporioides MA-299 and Structure Revision of Pandangolide 3
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00125openalex-snapshot
Polyketides and a Dihydroquinolone Alkaloid from a Marine-Derived Strain of the Fungus Metarhizium marquandii
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01277openalex-snapshot
Characterization of Cladosporols from the Marine Algal-Derived Endophytic Fungus Cladosporium cladosporioides EN-399 and Configurational Revision of the Previously Reported Cladosporol Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02421openalex-snapshot
Catalyst-Controlled Stereoselective Synthesis Secures the Structure of the Antimalarial Isocyanoterpene Pustulosaisonitrile-1
inferred← citeshttps://doi.org/10.1021/acs.joc.8b03037openalex-snapshot
Xylomolones A–D from the Thai Mangrove Xylocarpus moluccensis: Assignment of Absolute Stereostructures and Unveiling a Convergent Strategy for Limonoid Biosynthesis
inferred← citeshttps://doi.org/10.1021/acs.jpca.5b02332openalex-snapshot
Bicamphor: A Prototypic Molecular System to Investigate Vibrational Excitons
inferred← citeshttps://doi.org/10.1021/acs.jpcb.5b06590openalex-snapshot
A Novel Ferrocenyl Naphthoquinone Fused Crown Ether as a Multisensor for Water Determination in Acetonitrile and Selective Cation Binding
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c03613openalex-snapshot
Discovery of Three Macrocyclic Diterpenoid Skeletons from Croton laevigatus and Their NF-κB Inhibitory Activity
inferred← citeshttps://doi.org/10.1021/jp410370qopenalex-snapshot
Chiroptical Inversion Induced by Rotation of a Carbon–Carbon Single Bond: An Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1021/np500024ropenalex-snapshot
Polyhydroxy Cyclohexanols from aDendrodochiumsp. Fungus Associated with the Sea CucumberHolothuria nobilisSelenka
inferred← citeshttps://doi.org/10.1021/np500538copenalex-snapshot
Tetrahydroxanthene-1,3(2H)-dione Derivatives fromUvaria valderramensis
inferred← citeshttps://doi.org/10.1021/ol5001523openalex-snapshot
Penibruguieramine A, a Novel Pyrrolizidine Alkaloid from the Endophytic Fungus Penicillium sp. GD6 Associated with Chinese Mangrove Bruguiera gymnorrhiza
inferred← citeshttps://doi.org/10.1021/ol5007345openalex-snapshot
New Steroids with a Rearranged Skeleton as (h)P300 Inhibitors from the Sponge Theonella swinhoei
inferred← citeshttps://doi.org/10.1021/ol502649aopenalex-snapshot
Chiral Resolution and Absolute Configuration of a Pair of Rare Racemic Spirodienone Sesquineolignans from Xanthium sibiricum
inferred← citeshttps://doi.org/10.1039/c3ob42376jopenalex-snapshot
Chromane helicity rule – scope and challenges based on an ECD study of various trolox derivatives
inferred← citeshttps://doi.org/10.1039/c6ra27306hopenalex-snapshot
Daldinone derivatives from the mangrove-derived endophytic fungus Annulohypoxylon sp.
inferred← citeshttps://doi.org/10.1039/c7ra04941bopenalex-snapshot
Hydroquinone derivatives from the marine-derived fungus Gliomastix sp.
inferred← citeshttps://doi.org/10.1039/c7ra07351hopenalex-snapshot
Incensfuran: isolation, X-ray crystal structure and absolute configuration by means of chiroptical studies in solution and solid state
inferred← citeshttps://doi.org/10.1039/c8ob00789fopenalex-snapshot
Belamchinenin A, an unprecedented tricyclic-fused triterpenoid with cytotoxicity from Belamcanda chinensis
inferred← citeshttps://doi.org/10.1039/c8ra09067jopenalex-snapshot
Co-culture of the fungus Fusarium tricinctum with Streptomyces lividans induces production of cryptic naphthoquinone dimers
inferred← citeshttps://doi.org/10.1039/c9np00002jopenalex-snapshot
Applications of OR/ECD/VCD to the structure elucidation of natural products
inferred← citeshttps://doi.org/10.1039/d0ob00110dopenalex-snapshot
Synthesis and antiproliferative activity of 6-naphthylpterocarpans
inferred← citeshttps://doi.org/10.1039/d0ra03725gopenalex-snapshot
TDDFT-ECD and DFT-NMR studies of thaigranatins A–E and granatumin L isolated from Xylocarpus granatum
inferred← citeshttps://doi.org/10.1039/d2ra01701fopenalex-snapshot
Fluvirucins B 7 –B 10 , new antifungal macrolactams from a marine-derived Nonomuraea sp. MYH522
inferred← citeshttps://doi.org/10.1055/s-0037-1612085openalex-snapshot
1,2-Dihydrochromeno[2,3-c]pyrrol-3-one Derivatives: Synthesis and HPLC-ECD Analysis
inferred← citeshttps://doi.org/10.1080/05704928.2020.1831523openalex-snapshot
Electronic circular dichroism and Raman optical activity: Principle and applications
inferred← citeshttps://doi.org/10.1080/14786419.2018.1552699openalex-snapshot
Aspergillolide, a new 12-membered macrolide from sea cucumber-derived fungus Aspergillus sp. S-3-75
inferred← citeshttps://doi.org/10.1080/14786419.2019.1608543openalex-snapshot
Alternative total synthesis of dendrodolide-L
inferred← citeshttps://doi.org/10.11606/d.75.2023.tde-04102023-083958openalex-snapshot
Isolamento, identificação e derivatização de metabólitos secundários de fungos marinhos
inferred← citeshttps://doi.org/10.1177/1934578x1701200231openalex-snapshot
Isolation and Characterization of Antiangiogenesis Compounds from the Fungus Aspergillus terreus Associated with Apostichopus japonicus Using Zebrafish Assay
inferred← citeshttps://doi.org/10.14232/phd.3912openalex-snapshot
Bioactive secondary metabolites from Juncaceae species
inferred← citeshttps://doi.org/10.2174/0929867324666170310112009openalex-snapshot
Absolute Configuration Determination by Quantum Mechanical Calculation of Chiroptical Spectra: Basics and Applications to Fungal Metabolites
inferred← citeshttps://doi.org/10.24200/sci.2017.4602openalex-snapshot
Conformation of Gemcitabine: An Experimental NMR and Theoretical DFT Study
inferred← citeshttps://doi.org/10.3390/books978-3-0365-2753-6openalex-snapshot
Bioactive Marine Heterocyclic Compounds
inferred← citeshttps://doi.org/10.3390/ijms24065841openalex-snapshot
Isolation and NMR Scaling Factors for the Structure Determination of Lobatolide H, a Flexible Sesquiterpene from Neurolaena lobata
inferred← citeshttps://doi.org/10.3390/ijms25126453openalex-snapshot
Testing the Simplified Molecular Dynamics Approach to Improve the Reproduction of ECD Spectra and Monitor Aggregation
inferred← citeshttps://doi.org/10.3390/md12126178openalex-snapshot
Briarane Diterpenoids from the Gorgonian Dichotella gemmacea
inferred← citeshttps://doi.org/10.3390/md13063640openalex-snapshot
Peniciadametizine A, a Dithiodiketopiperazine with a Unique Spiro[furan-2,7'-pyrazino[1,2-b][1,2]oxazine] Skeleton, and a Related Analogue, Peniciadametizine B, from the Marine Sponge-Derived Fungus Penicillium adametzioides
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/md14110201openalex-snapshot
Chemistry and Bioactivity of Briaranes from the South China Sea Gorgonian Dichotella gemmacea
inferred← citeshttps://doi.org/10.3390/md15110359openalex-snapshot
Lactones from the Sponge-Derived Fungus Talaromyces rugulosus
inferred← citeshttps://doi.org/10.3390/md17050296openalex-snapshot
Polyketides from the Mangrove-Derived Endophytic Fungus Cladosporium cladosporioides
inferred← citeshttps://doi.org/10.3390/md17060339openalex-snapshot
Bioactive Compounds Isolated from Marine-Derived Microbes in China: 2009–2018
inferred← citeshttps://doi.org/10.3390/md18020073openalex-snapshot
Design of Fungal Co-Cultivation Based on Comparative Metabolomics and Bioactivity for Discovery of Marine Fungal Agrochemicals
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/md19080461openalex-snapshot
Culturable Microorganisms Associated with Sea Cucumbers and Microbial Natural Products
inferred← citeshttps://doi.org/10.3390/md22020070openalex-snapshot
Cytotoxic Compounds from Marine Fungi: Sources, Structures, and Bioactivity
inferred← citeshttps://doi.org/10.3390/metabo9100197openalex-snapshot
Extending the Metabolite Diversity of the Endophyte Dimorphosporicola tragani
inferred← citeshttps://doi.org/10.3390/molecules22101760openalex-snapshot
Glucopyranosylidene-Spiro-Thiazolinones: Synthetic Studies and Determination of Absolute Configuration by TDDFT-ECD Calculations
inferred← citeshttps://doi.org/10.3390/molecules26237377openalex-snapshot
Isolation and Identification of Pentalenolactone Analogs from Streptomyces sp. NRRL S-4
inferred← citeshttps://doi.org/10.3390/molecules27010198openalex-snapshot
Zizaane-Type Sesquiterpenoids and Their Rearranged Derivatives from Agarwood of an Aquilaria Plant
inferred← citeshttps://doi.org/10.3390/molecules27217650openalex-snapshot
Cytoprotective Polyketides from Sponge-Derived Fungus Lopadostoma pouzarii
inferred← citeshttps://doi.org/10.3762/bjoc.12.188openalex-snapshot
Varioloid A, a new indolyl-6,10b-dihydro-5aH-[1]benzofuro[2,3-b]indole derivative from the marine alga-derived endophytic fungus Paecilomyces variotii EN-291
inferred← citeshttps://doi.org/10.3762/bjoc.12.247openalex-snapshot
Biomimetic synthesis and HPLC–ECD analysis of the isomers of dracocephins A and B
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.75.522openalex-snapshot
Practical Use of Circular Dichroism and Vibrational Circular Dichroism for Structural Analysis
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.82.178openalex-snapshot
Note for Higher Reliability of Structural Analysis by Spectral Calculations
inferred← citeshttps://doi.org/10.5281/zenodo.26715openalex-snapshot
Myrmecological Notes. - New Australian Formicidae.
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.