Methoxatin as a Target in Total Synthesis


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SCHRÖDER, Birte, Tanja GAICH, 2017. Methoxatin as a Target in Total Synthesis. In: Synthesis. 49(08), pp. 1746-1756. ISSN 0039-7881. eISSN 1437-210X

@article{Schroder2017-03-30Metho-39027, title={Methoxatin as a Target in Total Synthesis}, year={2017}, doi={10.1055/s-0036-1589492}, number={08}, volume={49}, issn={0039-7881}, journal={Synthesis}, pages={1746--1756}, author={Schröder, Birte and Gaich, Tanja} }

<rdf:RDF xmlns:rdf="" xmlns:bibo="" xmlns:dc="" xmlns:dcterms="" xmlns:xsd="" > <rdf:Description rdf:about=""> <dc:creator>Gaich, Tanja</dc:creator> <dc:date rdf:datatype="">2017-05-24T09:16:44Z</dc:date> <dc:contributor>Gaich, Tanja</dc:contributor> <dcterms:available rdf:datatype="">2017-05-24T09:16:44Z</dcterms:available> <dc:language>eng</dc:language> <dcterms:issued>2017-03-30</dcterms:issued> <dcterms:abstract xml:lang="eng">Methoxatin is a redox co-factor with a unique structure featuring a central 1,2-benzoquinone, annulated to an electron-poor pyridine and an electron-poor pyrrole ring. This exceptional molecular structure leads to the unusual biological function of methoxatin, which therefore plays a significant role in metabolism. Hence, many total syntheses providing access to this remarkable natural product were published soon after the structure was elucidated.</dcterms:abstract> <bibo:uri rdf:resource=""/> <dc:contributor>Schröder, Birte</dc:contributor> <dc:creator>Schröder, Birte</dc:creator> <dcterms:title>Methoxatin as a Target in Total Synthesis</dcterms:title> </rdf:Description> </rdf:RDF>

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