Results 61 to 70 of about 175 (106)
Algae and Cyanobacteria Fatty Acids and Bioactive Metabolites: Natural Antifungal Alternative Against Fusarium sp. [PDF]
MicroorganismsLópez-Arellanes ME +3 more
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Synthetic Approach toward Structure Confirmation of Amphidinol 3
Synthetic Approach toward Structure Confirmation of Amphidinol 3openaire
Structure-based Study on Mode of Action of Dinoflagellate Metabolites, Amphidinols
Structure-based Study on Mode of Action of Dinoflagellate Metabolites, Amphidinolsopenaire
Structure Elucidation and Mode of Action of Amphidinol Homologues from Marine Dinoflagellate
Structure Elucidation and Mode of Action of Amphidinol Homologues from Marine Dinoflagellateopenaire
High Inter- and Intraspecific Variability in Amphidinol Content and Toxicity of Amphidinium Strains
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Total Synthesis of Amphidinol 3
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 2021Tohru Oishi
exaly +2 more sources
Amphidinol C, a major polyketide from an Irish strain of the dinoflagellate Amphidinium carterae
Phytochemistry Letters, 2022 An Irish strain of the dinoflagellate Amphidinium carterae was previously shown to produce antibacterial amphidinol derivatives of unknown masses. Inspection of the major metabolites present in a bulk culture of this strain led to the isolation and structure elucidation of a new amphidinol derivative named amphidinol C featuring an unprecedented ...
Maria Elena Barone, Olivier P Thomas
exaly +2 more sources
Journal of the American Chemical Society, 2020
Amphidinol 3 (AM3) is a potent antifungal produced by the dinoflagellate Amphidinium klebsii. It was difficult to determine the absolute configuration of AM3 by using the scarce natural product due to the presence of numerous stereogenic centers on the acyclic carbon chain.
Tohru Oishi +2 more
exaly +3 more sources
Amphidinol 3 (AM3) is a potent antifungal produced by the dinoflagellate Amphidinium klebsii. It was difficult to determine the absolute configuration of AM3 by using the scarce natural product due to the presence of numerous stereogenic centers on the acyclic carbon chain.
Tohru Oishi +2 more
exaly +3 more sources
Synthesis of the C31—C67 Fragment of Amphidinol 3.
ChemInform, 2006AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Javier, de Vicente +2 more
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Convergent Synthesis of the C18-C30 Fragment of Amphidinol 3
Synlett, 2009The C18-C30 fragment of amphidinol 3 has been synthesized in a convergent fashion by employing two asymmetric Sharpless dihydroxylations, a Julia-Kocienski olefination and a Wittig reaction as the key steps.
Janine Cossy
exaly +2 more sources