Keywords
aryl hydroxamates
C-H activation
diazo compounds
isoindolones
organofluorine compounds.
rhodium(iii) catalysis
Abstract
An efficient method for the selective preparation of trifluoro-methyl-substituted isoindolones has been developed via RhIII catalyzed C-H activation / [4 + 1]-annulation of aryl hydroxamates with functionalized acceptor/acceptor diazo compounds as cross-coupling partners.
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