The Witkop Cyclization : A Photoinduced C-H Activation of the Indole System

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GRITSCH, Philipp, Christian LEITNER, Magnus PFAFFENBACH, Tanja GAICH, 2014. The Witkop Cyclization : A Photoinduced C-H Activation of the Indole System. In: Angewandte Chemie International Edition. 53(5), pp. 1208-1217. ISSN 1433-7851. eISSN 1521-3773

@article{Gritsch2014-01-27Witko-38080, title={The Witkop Cyclization : A Photoinduced C-H Activation of the Indole System}, year={2014}, doi={10.1002/anie.201307391}, number={5}, volume={53}, issn={1433-7851}, journal={Angewandte Chemie International Edition}, pages={1208--1217}, author={Gritsch, Philipp and Leitner, Christian and Pfaffenbach, Magnus and Gaich, Tanja} }

<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/123456789/38080"> <dcterms:issued>2014-01-27</dcterms:issued> <dcterms:title>The Witkop Cyclization : A Photoinduced C-H Activation of the Indole System</dcterms:title> <dc:contributor>Leitner, Christian</dc:contributor> <dc:creator>Pfaffenbach, Magnus</dc:creator> <bibo:uri rdf:resource="https://kops.uni-konstanz.de/handle/123456789/38080"/> <dc:creator>Gaich, Tanja</dc:creator> <dc:language>eng</dc:language> <dc:contributor>Gritsch, Philipp</dc:contributor> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2017-03-21T10:00:57Z</dcterms:available> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2017-03-21T10:00:57Z</dc:date> <dcterms:abstract xml:lang="eng">Investigations of excited-state redox processes have an exceptional impact on the field of organic photochemistry and its application to the synthesis of complex target molecules. In such a photochemical process a single-electron transfer takes place to produce ion-radical intermediates, if the reduction and oxidation potentials, as well as excited-state energies of electron donors and acceptors are chosen appropriately. The Witkop cyclization constitutes an intramolecular variant of such a process, typically with an indole heterocycle as an electron donor. The specific synthetic value of this reaction lies in a C-C bond formation without requiring any prefunctionalization of the indole system. Although this photoreaction has been applied to the total synthesis of natural products, it has still not been used to its full capacity. The following review details synthetic efforts using the Witkop cyclization, and aims to incite further applications of reaction in the synthesis of complex molecular architectures.</dcterms:abstract> <dc:contributor>Pfaffenbach, Magnus</dc:contributor> <dc:creator>Gritsch, Philipp</dc:creator> <dc:creator>Leitner, Christian</dc:creator> <dc:contributor>Gaich, Tanja</dc:contributor> </rdf:Description> </rdf:RDF>

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