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Photoenolisierung von ortho-Alkyl-substituierten Phenylketonen"},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904665"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904664","@type":"sc:Range","label":"2.1.6  Energie-Transfer"},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904667"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904666","@type":"sc:Range","label":"2.1.7  Photoinduzierter Elektron-Transfer"},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904669"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904668","@type":"sc:Range","label":"2.2.1  Photochemie von Butyrophenon"},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904671"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904670","@type":"sc:Range","label":"2.2.2  Photochemische Bildung von 1,2-Dibenzoylethan aus 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 Denkbare Reaktionsm\u00f6glichkeiten im Butyrophenon-System"},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904679"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904678","@type":"sc:Range","label":"Die Komponenten des Butyrophenon-Systems k\u00f6nnten involviert sein in verschiedene denkbare Additions-, HAT- und Rekombinationsschritte (zweiseitiges Schema 11).  In die Betrachtung sind u.a. in der Literatur berichtete Reaktionsm\u00f6glichkeiten des Aceton..."},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904690"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904689","@type":"sc:Range","label":"\u00dcberlegungen zur \u03b1-C-Substitution der aromatischen Ketone des Butyrophenon-Systems: Das Acetophenon-System kann als ein Ma\u00df f\u00fcr die Effizienz der \u03b1-C-H-Abstraktion im Fall ohne Alkyl-Substitution betrachtet werden. Im ethyl-substituierten Butyrophenon..."},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904697","https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904698"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904696","@type":"sc:Range","label":"- Weg 11: Ketylradikale k\u00f6nnten als C-HAT-Donatoren agieren, wodurch Enolformen gebildet w\u00fcrden (Analogieschluss) [8,23,57\u201359]. Zwei Ketylradikale k\u00f6nnten disproportionieren (\u201eDismutation\u201c) [127,135].  Acetophenon l\u00e4ge im thermodynamischen Gleichgewic..."},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904700"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904699","@type":"sc:Range","label":"Beim Butyrophenon-System ist Letzteres a priori betrachtet m\u00f6glicherweise nicht ganz identisch, da der Ethylrest an der \u03b1-Position sowohl die \u03b1-C-H-Bindung destabilisieren bzw. radikalisch abstrahierbar machen k\u00f6nnte als auch eine eventuell gebildete ..."},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904705"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904704","@type":"sc:Range","label":"Additionen:"},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904716","https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904717","https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904718"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904715","@type":"sc:Range","label":"2.2.6  Reaktionsverlauf bei Enolisierung von Acetophenon durch alkoholische Katalyse"},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904721","https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904722","https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904723"],"ranges":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904720"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904719","@type":"sc:Range","label":"2.2.7  Denkbarer Kupplungsweg via Light Absorbing Transients"},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904721","https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904722","https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904723"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904720","@type":"sc:Range","label":"- Weg L3: Der gleiche Analogieschluss zum Acetophenon- und Benzophenon-Themenkreis gilt f\u00fcr die Bildung von intermolekularen LATs. 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Temperaturabh\u00e4ngigkeit"},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904769"],"ranges":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904768","https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904770","https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904771","https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904772","https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904773","https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904774"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904767","@type":"sc:Range","label":"3.3.4  Untersuchungen zum Wassergehalt des L\u00f6semittels"},{"canvases":["https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/canvas/3904769"],"@id":"https://elekpub.bib.uni-wuppertal.de/i3f/v20/3552819/range/3904768","@type":"sc:Range","label":"Die meisten Experimente dieser Arbeit wurden aufgrund pragmatischer \u00dcberlegungen bzw. finanzieller und 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