Photosensitizer-free, gold-catalyzed c-c cross-coupling of boronic acids and diazonium salts enabled by visible light

The first photosensitizer-free visible light-driven, gold-catalyzed C-C cross-couplings of arylboronic acids and aryldiazonium salts are reported. The reactions can be conducted under very mild conditions, using a catalytic amount of tris(4-trifluoromethyl)phosphinegold(I) chloride [(4-CF3-C6H4)3PAu...

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Bibliographic Details
Main Authors: Witzel, Sina (Author) , Xie, Jin (Author) , Rudolph, Matthias (Author) , Hashmi, A. Stephen K. (Author)
Format: Article (Journal)
Language:English
Published: March 20, 2017
In: Advanced synthesis & catalysis
Year: 2017, Volume: 359, Issue: 9, Pages: 1522-1528
ISSN:1615-4169
DOI:10.1002/adsc.201700121
Online Access:Verlag, Volltext: http://dx.doi.org/10.1002/adsc.201700121
Verlag, Volltext: http://onlinelibrary.wiley.com/doi/10.1002/adsc.201700121/epdf
Verlag, Volltext: http://onlinelibrary.wiley.com/doi/10.1002/adsc.201700121/abstract
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Author Notes:Sina Witzel, Jin Xie, Matthias Rudolph, A. Stephen K. Hashmi
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Summary:The first photosensitizer-free visible light-driven, gold-catalyzed C-C cross-couplings of arylboronic acids and aryldiazonium salts are reported. The reactions can be conducted under very mild conditions, using a catalytic amount of tris(4-trifluoromethyl)phosphinegold(I) chloride [(4-CF3-C6H4)3PAuCl] with methanol as the solvent allowing an alternative access to a variety of substituted biaryls in moderate to excellent yields with broad functional group tolerance.
Item Description:Gesehen am 28.08.2017
Physical Description:Online Resource
ISSN:1615-4169
DOI:10.1002/adsc.201700121