Results 91 to 100 of about 276 (135)

Synthetic Approach toward Structure Confirmation of Amphidinol 3

, 2011
openaire   +1 more source

Algae and Cyanobacteria Fatty Acids and Bioactive Metabolites: Natural Antifungal Alternative Against Fusarium sp. [PDF]

Microorganisms
López-Arellanes ME, López-Pacheco LD, Elizondo-Luevano JH, González-Meza GM.   +3 more
europepmc   +1 more source

Synthetic Approach toward Structure Confirmation of Amphidinol 3

Synthetic Approach toward Structure Confirmation of Amphidinol 3
openaire  

Structure-based Study on Mode of Action of Dinoflagellate Metabolites, Amphidinols

Structure-based Study on Mode of Action of Dinoflagellate Metabolites, Amphidinols
openaire  

Structure Elucidation and Mode of Action of Amphidinol Homologues from Marine Dinoflagellate

Structure Elucidation and Mode of Action of Amphidinol Homologues from Marine Dinoflagellate
openaire  

High Inter- and Intraspecific Variability in Amphidinol Content and Toxicity of Amphidinium Strains

openaire   +1 more source

Convergent Synthesis of the C18-C30 Fragment of Amphidinol 3

Synlett, 2009
The 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, Sébastien Reymond, Françoise Colobert   +2 more
exaly   +3 more sources

Total Synthesis of Amphidinol 3: A General Strategy for Synthesizing Amphidinol Analogues and Structure–Activity Relationship Study

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.
Yuma Wakamiya, Makoto Ebine, Nobuaki Matsumori, Tohru Oishi   +3 more
openaire   +3 more sources

Stereoselective Synthesis of the C(1) - C(28) Fragment of Amphidinol 3

Helvetica Chimica Acta, 2016
A stereoselective synthesis of the polyol side chain (C(1) – C(28)) of amphidinol 3 has been accomplished following Sharpless epoxidation, Crimmins aldol reaction, Jacobsen kinetic resolution, Sharpless asymmetric dihydroxylation, and our own reaction ...
Jhillu S Yadav, B V Subba Reddy
exaly   +3 more sources

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Synthesis of the C31–C67 Fragment of Amphidinol 3

Angewandte Chemie - International Edition, 2006
AbstractChemInform 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.
Scott D Rychnovsky
exaly   +3 more sources