Oxidative gold catalysis meets photochemistry - synthesis of benzo(a)fluorenones from diynes

Diynes bearing one terminal and one triarylmethyl-substituted alkyne were converted into complex benzofluorenone derivatives via a one-pot process involving a gold-catalyzed step followed by a photocyclization/oxidation. In the first step an N-oxide was used to position-selectively generate an α-oxo...

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Hauptverfasser: Nösel, Pascal (VerfasserIn) , Hendrich, Christoph (VerfasserIn) , Rudolph, Matthias (VerfasserIn) , Rominger, Frank (VerfasserIn) , Hashmi, A. Stephen K. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 14 November 2014
In: Advanced synthesis & catalysis
Year: 2014, Jahrgang: 356, Heft: 18, Pages: 3755-3760
ISSN:1615-4169
DOI:10.1002/adsc.201400969
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/adsc.201400969
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/adsc.201400969
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Verfasserangaben:Pascal Nösel, Setareh Moghimi, Christoph Hendrich, Marten Haupt, Matthias Rudolph, Frank Rominger, and A. Stephen K. Hashmi
Beschreibung
Zusammenfassung:Diynes bearing one terminal and one triarylmethyl-substituted alkyne were converted into complex benzofluorenone derivatives via a one-pot process involving a gold-catalyzed step followed by a photocyclization/oxidation. In the first step an N-oxide was used to position-selectively generate an α-oxo carbenoid at the terminal alkyne which after a regioselective 1,6-carbene transfer along the tethered tritylalkyne and a subsequent aryl 1,2-shift furnished tetraphenylethylene-like derivatives. These intermediates were successfully transformed to fluorenones via oxidative photocyclization.
Beschreibung:Im Titel ist der Buchstabe "a" in eckigen Klammern
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Beschreibung:Online Resource
ISSN:1615-4169
DOI:10.1002/adsc.201400969