| Attributes | Values |
|---|
| rdf:type
| |
| description
| - wetenschappelijk artikel (nl)
- наукова стаття, опублікована в липні 1984 (uk)
- im Juli 1984 veröffentlichter wissenschaftlicher Artikel (de)
- artículu científicu espublizáu en xunetu de 1984 (ast)
- scientific article published on 01 July 1984 (en)
|
| publication date
| |
| publication date
| |
| language of work or name
| |
| language of work or name
| |
| cites work
| |
| cites work
| |
| access restriction status
| |
| access restriction status
| |
| author name string
| |
| author name string
| - M Yamada
- M Fujita
- K Kawai
- S Nakajima
- M Nagai
|
| rdfs:label
| - O-Methylation effect on the carbon-13 nuclear magnetic resonance signals of ortho-disubstituted phenols and its application to structure determination of new phthalides from Aspergillus silvaticus (en)
- O-Methylation effect on the carbon-13 nuclear magnetic resonance signals of ortho-disubstituted phenols and its application to structure determination of new phthalides from Aspergillus silvaticus (nl)
|
| skos:prefLabel
| - O-Methylation effect on the carbon-13 nuclear magnetic resonance signals of ortho-disubstituted phenols and its application to structure determination of new phthalides from Aspergillus silvaticus (en)
- O-Methylation effect on the carbon-13 nuclear magnetic resonance signals of ortho-disubstituted phenols and its application to structure determination of new phthalides from Aspergillus silvaticus (nl)
|
| name
| - O-Methylation effect on the carbon-13 nuclear magnetic resonance signals of ortho-disubstituted phenols and its application to structure determination of new phthalides from Aspergillus silvaticus (en)
- O-Methylation effect on the carbon-13 nuclear magnetic resonance signals of ortho-disubstituted phenols and its application to structure determination of new phthalides from Aspergillus silvaticus (nl)
|
| title
| |
| title
| - O-Methylation effect on the carbon-13 nuclear magnetic resonance signals of ortho-disubstituted phenols and its application to structure determination of new phthalides from Aspergillus silvaticus (en)
|
| page(s)
| |
| page(s)
| |
| instance of
| |
| instance of
| |
| main subject
| |
| main subject
| |
| PubMed ID
| |
| PubMed ID
| |
| PubMed ID
| |
| published in
| |
| full work available at URL
| |
| published in
| |
| full work available at URL
| |
| issue
| |
| volume
| |
| issue
| |
| volume
| |
| DOI
| |
| DOI
| |
| DOI
| |
| online access status
| |
| online access status
| |
| is about
of | |
| is cites work
of | - Tagetolone and tagetenolone: two phytotoxic polyketides from Alternaria tagetica
- Structures of new flavonoids and benzofuran-type stilbene and degranulation inhibitors of rat basophilic leukemia cells from the Brazilian herbal medicine Cissus sicyoides
- Bioactive constituents from Chinese natural medicines. XVII. constituents with radical scavenging effect and new glucosyloxybenzyl 2-isobutylmalates from Gymnadenia conopsea
- Antidiabetic principles of natural medicines. II. Aldose reductase and alpha-glucosidase inhibitors from Brazilian natural medicine, the leaves of Myrcia multiflora DC. (Myrtaceae): structures of myrciacitrins I and II and myrciaphenones A and B.
- Benzoic acid allopyranosides from the bark of Pseudolarix kaempferi
- Determination of iodide with 1,3-dibromo-5,5-dimethylhydantoin (DBH) in comparison with the ICl-method. Analytical methods of pharmacopeias with DBH in respect to environmental and economical concern. Part 3.
- Studies on fungal products. XVI. New metabolites related to 3-methylorsellinate from Aspergillus silvaticus
- Metabolites of orally administered Magnolia officinalis extract in rats and man and its antidepressant-like effects in mice
- Rapid extract dereplication using HPLC-SPE-NMR: analysis of isoflavonoids from Smirnowia iranica
- Marilones A-C, phthalides from the sponge-derived fungus Stachylidium sp
- Acetophthalidin, a novel inhibitor of mammalian cell cycle, produced by a fungus isolated from a sea sediment
- Phthalides and phthalans: synthetic methodologies and their applications in the total synthesis.
- Cytotoxic compounds from Polygala vulgaris
- Identification and molecular genetic analysis of the cichorine gene cluster in Aspergillus nidulans.
- [Constituents of Acer nikoense and Myrica rubra. On diarylheptanoids]
- Matrix-dependent cationization in MALDI mass spectrometry
- Penicisochromans from the endophytic fungus Penicillium sp. BCC18034
- Two myricanol glycosides from Myrica rubra and revision of the structure of isomyricanone
- Natural zinniol derivatives from Alternaria tagetica. Isolation, synthesis, and structure-activity correlation.
- Syntheses of two cytotoxic sinapyl alcohol derivatives and isolation of four new related compounds from Ligularia nelumbifolia
- Cyclooxygenase inhibitory and antioxidant compounds from the fruiting body of an edible mushroom, Agrocybe aegerita
- Two new zinniol-related phytotoxins from Alternaria solani
- First total synthesis of cichorine and zinnimidine
- Porritoxinol, a phytotoxin of Alternaria porri
- Phthalides: Distribution in Nature, Chemical Reactivity, Synthesis, and Biological Activity
- Spectroscopic Properties and Conformational Analysis of Methyl Ester of Sinapic Acid in Various Environments
- Novel antimicrobial metabolites produced by Sika deer-associated Actinomyces sp. JN411010.
- Tetrahydroxanthone-chromanone heterodimers from lichen Usnea aciculifera and their cytotoxic activity against human cancer cell lines
- Beshanzoides A-D, unprecedented cycloheptanone-containing polyketides from <i>Penicillium commune</i> P-4-1, an endophytic fungus of the endangered conifer <i>Abies beshanzuensis</i>
- Nitric oxide inhibitory polyketides from Penicillium chrysogenum MT-12, an endophytic fungus isolated from Huperzia serrata.
- Talarolactone A, an Isocoumarin Derivative Fused with Dihydrothiophene with Selective Antimigratory Activity from the Endolichenic Fungus Talaromyces sp
- Microbial Natural Products That Affect Plants, Phytopathogens, and Certain other Microorganisms
- Stereoelectronic effects on 1H nuclear magnetic resonance chemical shifts in methoxybenzenes
- Discovery of Three New Phytotoxins from the Fungus by Pathway Inactivation
|
| is cites work
of | |
![[RDF Data]](/fct/images/sw-rdf-blue.png)
![[cxml]](/fct/images/cxml_doc.png)
![[csv]](/fct/images/csv_doc.png)
![[text]](/fct/images/ntriples_doc.png)
![[turtle]](/fct/images/n3turtle_doc.png)
![[ld+json]](/fct/images/jsonld_doc.png)
![[rdf+json]](/fct/images/json_doc.png)
![[rdf+xml]](/fct/images/xml_doc.png)
![[atom+xml]](/fct/images/atom_doc.png)
![[html]](/fct/images/html_doc.png)