Highly substituted indol-2-ones, quinoxalin-2-ones and benzodiazepin-2,5-diones via a new Ugi(4CR)-Pd assisted N-aryl amidation strategy

A new strategy employing an Ugi four-component reaction and a palladium-assisted intramolecular N-aryl amidation reaction is reported. The straight forward two-step synthesis generates N-heterocyclic compounds with four points of diversity from trivial starting materials with acceptable yields. This new reaction is also suitable for the generation of compound libraries.

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