α-Arylation of alkylamines with sulfonylarenes through a radical chain mechanism
In the presence of a substoichiometric amount of a tert -butoxy radical precursor, the reaction of alkylamines with sulfonylarenes was found to give α-arylated alkylamines through homolytic aromatic substitution, where a radical chain is operative. A radical chain, conducted by a sulfonyl radical in...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2018-09, Vol.54 (74), p.1471-1474 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In the presence of a substoichiometric amount of a
tert
-butoxy radical precursor, the reaction of alkylamines with sulfonylarenes was found to give α-arylated alkylamines through homolytic aromatic substitution, where a radical chain is operative.
A radical chain, conducted by a sulfonyl radical in a homolytic aromatic substitution mechanism, makes it possible to promote α-arylation of alkylamines with sulfonylarenes just by using a substoichiometric amount of a
tert
-butoxy radical precursor. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c8cc03604g |