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First synthesis of naphthalene annulated oxepins

Dobelmann, Lars, Parham, A. H., Büsing, A., Buchholz, H. and König, Burkhard (2014) First synthesis of naphthalene annulated oxepins. RSC Advances 4, pp. 60473-60477.

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Date of publication of this fulltext: 17 Nov 2014 07:09

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Highly condensed oxepins have been prepared in good yields from their corresponding diols by etherification using p-toluenesulfonic acid. Their intriguing twisted structures were unambiguously determined by X-ray crystallography. Substitution effects of a novel highly aromatic naphthalene annulated oxepin indicate that structural and conjugative effects have an influence on the optoelectronic properties.

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Item type:Article
Additional Information (public):Open-Access-Komponente aus der Allianzlizenz
Institutions:Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Burkhard König
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Dewey Decimal Classification:500 Science > 540 Chemistry & allied sciences
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Yes
Item ID:30965
Owner only: item control page


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