Light-Mediated Total Synthesis of 17-Deoxyprovidencin

Zitieren

Dateien zu dieser Ressource

Dateien Größe Format Anzeige

Zu diesem Dokument gibt es keine Dateien.

TOELLE, Nina, Harald WEINSTABL, Tanja GAICH, Johann MULZER, 2014. Light-Mediated Total Synthesis of 17-Deoxyprovidencin. In: Angewandte Chemie International Edition. 53(15), pp. 3859-3862. ISSN 1433-7851. eISSN 1521-3773

@article{Toelle2014-04-07Light-38414, title={Light-Mediated Total Synthesis of 17-Deoxyprovidencin}, year={2014}, doi={10.1002/anie.201400617}, number={15}, volume={53}, issn={1433-7851}, journal={Angewandte Chemie International Edition}, pages={3859--3862}, author={Toelle, Nina and Weinstabl, Harald and Gaich, Tanja and Mulzer, Johann} }

<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/rdf/resource/123456789/38414"> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2017-04-07T08:26:58Z</dc:date> <dc:creator>Toelle, Nina</dc:creator> <dc:contributor>Mulzer, Johann</dc:contributor> <dc:contributor>Weinstabl, Harald</dc:contributor> <dc:language>eng</dc:language> <dc:contributor>Toelle, Nina</dc:contributor> <dcterms:issued>2014-04-07</dcterms:issued> <bibo:uri rdf:resource="https://kops.uni-konstanz.de/handle/123456789/38414"/> <dc:creator>Weinstabl, Harald</dc:creator> <dcterms:title>Light-Mediated Total Synthesis of 17-Deoxyprovidencin</dcterms:title> <dc:creator>Gaich, Tanja</dc:creator> <dc:contributor>Gaich, Tanja</dc:contributor> <dc:creator>Mulzer, Johann</dc:creator> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2017-04-07T08:26:58Z</dcterms:available> <dcterms:abstract xml:lang="eng">An asymmetric synthesis of the diterpenoid 17-deoxyprovidencin is described. Key steps include an aldol addition, a base-catalyzed Wipf-type furan formation, a Z-selective ring-closing metathesis for macrocyclization, a photochemical E/Z isomerization to a highly strained and conformationally restricted ring system, and the stereoselective formation of two epoxides on the ring.</dcterms:abstract> </rdf:Description> </rdf:RDF>

Das Dokument erscheint in:

KOPS Suche


Stöbern

Mein Benutzerkonto