Type of Publication: | Journal article |
Publication status: | Published |
Author: | Pfaffenbach, Magnus; Roller, Alexander; Gaich, Tanja |
Year of publication: | 2016 |
Published in: | Chemistry - A European Journal ; 22 (2016), 25. - pp. 8444-8447. - ISSN 0947-6539. - eISSN 1521-3765 |
Pubmed ID: | 27037758 |
DOI (citable link): | https://dx.doi.org/10.1002/chem.201600835 |
Summary: |
Herein, we report the synthetically practical, short, and general access to novel indolophane architectures by means of a photochemical C-H activation process-the Witkop cyclization. These highly strained scaffolds were obtained by photoinduced ring closure and feature atropisomerism as well as aromatic ring current effects, which both have been investigated. The prevailing regioselectivity of theWitkop cyclization reaction was completely reversed by the presence of a quaternary carbon center, exerting a strong Thorpe-Ingold effect on the system for which experimental-evidence is provided.
|
Subject (DDC): | 540 Chemistry |
Bibliography of Konstanz: | Yes |
Files | Size | Format | View |
---|---|---|---|
There are no files associated with this item. |
PFAFFENBACH, Magnus, Alexander ROLLER, Tanja GAICH, 2016. Synthesis of Indolophanes by Photochemical Macrocyclization. In: Chemistry - A European Journal. 22(25), pp. 8444-8447. ISSN 0947-6539. eISSN 1521-3765. Available under: doi: 10.1002/chem.201600835
@article{Pfaffenbach2016Synth-35521, title={Synthesis of Indolophanes by Photochemical Macrocyclization}, year={2016}, doi={10.1002/chem.201600835}, number={25}, volume={22}, issn={0947-6539}, journal={Chemistry - A European Journal}, pages={8444--8447}, author={Pfaffenbach, Magnus and Roller, Alexander and Gaich, Tanja} }
<rdf:RDF xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:void="http://rdfs.org/ns/void#" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/rdf/resource/123456789/35521"> <dcterms:title>Synthesis of Indolophanes by Photochemical Macrocyclization</dcterms:title> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/rdf/resource/123456789/29"/> <bibo:uri rdf:resource="https://kops.uni-konstanz.de/handle/123456789/35521"/> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/rdf/resource/123456789/29"/> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dc:creator>Pfaffenbach, Magnus</dc:creator> <dc:language>eng</dc:language> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2016-10-11T08:25:53Z</dcterms:available> <dc:creator>Gaich, Tanja</dc:creator> <dcterms:abstract xml:lang="eng">Herein, we report the synthetically practical, short, and general access to novel indolophane architectures by means of a photochemical C-H activation process-the Witkop cyclization. These highly strained scaffolds were obtained by photoinduced ring closure and feature atropisomerism as well as aromatic ring current effects, which both have been investigated. The prevailing regioselectivity of theWitkop cyclization reaction was completely reversed by the presence of a quaternary carbon center, exerting a strong Thorpe-Ingold effect on the system for which experimental-evidence is provided.</dcterms:abstract> <dc:creator>Roller, Alexander</dc:creator> <dc:contributor>Gaich, Tanja</dc:contributor> <dcterms:issued>2016</dcterms:issued> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2016-10-11T08:25:53Z</dc:date> <dc:contributor>Roller, Alexander</dc:contributor> <foaf:homepage rdf:resource="http://localhost:8080/jspui"/> <dc:contributor>Pfaffenbach, Magnus</dc:contributor> </rdf:Description> </rdf:RDF>