Beilstein Journal of Organic Chemistry (Jun 2014)

Asymmetric Ugi 3CR on isatin-derived ketimine: synthesis of chiral 3,3-disubstituted 3-aminooxindole derivatives

  • Giordano Lesma,
  • Fiorella Meneghetti,
  • Alessandro Sacchetti,
  • Mattia Stucchi,
  • Alessandra Silvani

DOI
https://doi.org/10.3762/bjoc.10.141
Journal volume & issue
Vol. 10, no. 1
pp. 1383 – 1389

Abstract

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An efficient Ugi three-component reaction of a preformed chiral ketimine derived from isatin with various isonitrile and acid components has been developed. The reactions proceeded smoothly and in a stereocontrolled manner with regard to the new center of the Ugi products due to the stereoinduction of the amine chiral residue. A wide variety of novel chiral 3,3-disubstituted 3-aminooxindoles were obtained, a selection of which were subjected to post-Ugi transformations, paving the way to application as peptidomimetics.

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