An organoselenium-catalyzed C2,3-diarylation
of unprotected N–H
indoles with electron-rich aromatics has been developed. This one-pot
multicomponent tandem cross-dehydrogenation coupling reaction allows
for the incorporation of two different aromatic groups to indoles.
More importantly, this approach offers significant advantages, including
a high atom and step economy, eliminating the need for prepreparation
of the reaction substrates, streamlining the synthetic process and
enhancing its practicality. Overall, this organoselenium-catalyzed
C2,3-diarylation reaction presents an efficient and versatile strategy
for the functionalization of indole derivatives.