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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
26
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pubmed:dateCreated |
2003-12-19
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pubmed:abstractText |
An azaspiro[5.5]undecadiene corresponding to a subunit of the shellfish toxin gymnodimine was synthesized by Diels-Alder cycloaddition. One member of the pair of stereoisomeric adducts was transformed to a spiroimine, which will serve as the core around which the macrocyclic portion of the toxin will be assembled. [structure: see text]
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1523-7060
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
25
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pubmed:volume |
5
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4983-6
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:14682745-Animals,
pubmed-meshheading:14682745-Crystallography, X-Ray,
pubmed-meshheading:14682745-Cyclization,
pubmed-meshheading:14682745-Heterocyclic Compounds, 3-Ring,
pubmed-meshheading:14682745-Hydrocarbons, Cyclic,
pubmed-meshheading:14682745-Imines,
pubmed-meshheading:14682745-Indicators and Reagents,
pubmed-meshheading:14682745-Marine Toxins,
pubmed-meshheading:14682745-Models, Molecular,
pubmed-meshheading:14682745-Molecular Conformation,
pubmed-meshheading:14682745-Ostreidae
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pubmed:year |
2003
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pubmed:articleTitle |
Studies on the synthesis of gymnodimine. construction of the spiroimine portion via Diels-Alder cycloaddition.
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pubmed:affiliation |
Department of Chemistry, Oregon State University, Corvallis, OR 97331-4003, USA. james.white@orst.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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