What is it about?
A versatile route has been developed for the synthesis of 2‐arylindoles using a Pd‐catalyzed tandem process. Under reductive conditions, different 2‐arylindoles were synthesized from phenylglyoxal and aniline. This synthetic methodology involves a tandem reaction of four steps with high regioselectivity. Alternatively, 2‐anilinoacetophenones intermediates also can be using to give access to the corresponding 2‐arylindoles.
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Why is it important?
we report a synthesis of 2-arylindoles with high regioselectivity and good yields through a sequential condensat ion/reductive amination using a palladium catalyst under reductive conditions.
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This page is a summary of: Regioselective Synthesis of 2-Arylindoles via Palladium-Catalyzed Cyclization of Phenylglyoxal and 2-Anilinoacetophenones with Anilines, European Journal of Organic Chemistry, June 2019, Wiley,
DOI: 10.1002/ejoc.201900394.
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