Copper catalyzed oxidative coupling reactions for trifluoromethylselenolations--synthesis of R-SeCF3 compounds using air stable tetramethylammonium trifluoromethylselenate

The aerobic, room-temperature coupling of tetramethylammonium trifluoromethylselenate with readily available boronic acids, boronic esters, and terminal alkynes has been developed. The method permits direct access to valuable trifluoromethylselenoarenes and alkynes under mild conditions. A convenien...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2015-03, Vol.51 (21), p.4394-4397
Hauptverfasser: Lefebvre, Quentin, Pluta, Roman, Rueping, Magnus
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container_title Chemical communications (Cambridge, England)
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creator Lefebvre, Quentin
Pluta, Roman
Rueping, Magnus
description The aerobic, room-temperature coupling of tetramethylammonium trifluoromethylselenate with readily available boronic acids, boronic esters, and terminal alkynes has been developed. The method permits direct access to valuable trifluoromethylselenoarenes and alkynes under mild conditions. A convenient one-pot reaction, a scale up procedure as well as an extension to perfluoroalkylselenates are also presented to further demonstrate the synthetic utility of this reaction.
doi_str_mv 10.1039/c4cc10212f
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title Copper catalyzed oxidative coupling reactions for trifluoromethylselenolations--synthesis of R-SeCF3 compounds using air stable tetramethylammonium trifluoromethylselenate
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