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gymnodimine

National Institutes of Health

Related topics

Related topics

3 relations

Broader (3)

Heterocyclic Compounds, 3-RingHydrocarbons, CyclicImines

Papers overview

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2019
2019
An Approach towards the Synthesis of the Spiroimine Fragment of 13-Desmethylspirolide C and Gymnodimine A.
A general access to the spiroimine skeleton of gymnodimine and spirolides is described, relying on the construction of the… 
2015
2015
Bioaccumulation of Trace Metals in Mussel (Mytilus galloprovincialis) from Mali Ston Bay during DSP Toxicity Episodes
The Croatian National Monitoring Program revealed the presence of Diarrhetic Shellfish Poisoning (DSP) toxicity in Mediterranean… 
2011
2011
Marine algal pinnatoxins E and F cause neuromuscular block in an in vitro hemidiaphragm preparation.
2011
2011
Latitudinal transects in the southeastern Pacific Ocean reveal a diverse but patchy distribution of phycotoxins.
2010
2010
Feasibility of gymnodimine and 13-desmethyl C spirolide detection by fluorescence polarization using a receptor-based assay in shellfish matrixes.
Review
2009
Review
2009
[Cyclic imine toxin gymnodimine: a review].
Gymnodimine (GYM), an algal toxin first detected from New Zealand oysters in 1994, is identified as a cyclic imine toxin and… 
2005
2005
Biomimetic macrocycle-forming Diels-Alder reaction of an iminium dienophile: synthetic studies directed toward gymnodimine.
The macrocyclic core of gymnodimine has been constructed via an intramolecular Diels-Alder reaction of an alpha,beta-unsaturated… 
2005
2005
Studies toward a marine toxin immunogen: enantioselective synthesis of the spirocyclic imine of (-)-gymnodimine.
[reaction: see text] An enantioselective Diels-Alder reaction catalyzed by an Evans' copper-bis(oxazoline) complex was utilized… 
2003
2003
Studies on the synthesis of gymnodimine. construction of the spiroimine portion via Diels-Alder cycloaddition.
An azaspiro[5.5]undecadiene corresponding to a subunit of the shellfish toxin gymnodimine was synthesized by Diels-Alder… 
2001
2001
Studies toward gymnodimine: development of a single-pot Hua reaction for the synthesis of highly hindered cyclic imines.
[structure: see text]. In studies directed toward gymnodimine and related marine toxins, a single-pot variation of the Hua cyclic… 
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