Abstract

Abstract A green Passerini three-component reaction of 2-(4-oxo-4,5,6,7-tetrahydro-1 H -indol-1-yl)acetic acid with alkyl or aryl isocyanides and aldehydes was reported under aqueous conditions at 35 °C for 1 h, and 21 indolone- N -amino acid derivatives were prepared in high yields of 42%–99%. Their structures were characterized by IR, ESI–MS, NMR and elemental analysis, and the possible mechanisms have been also proposed. The highly efficient and eco-friendly method provides a facile access to a library of indolone- N -amino acid derivatives for future research on bioactivity screening.

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