Beilstein Journal of Organic Chemistry (Oct 2011)

Continuous-flow enantioselective α-aminoxylation of aldehydes catalyzed by a polystyrene-immobilized hydroxyproline

  • Xacobe C. Cambeiro,
  • Rafael Martín-Rapún,
  • Pedro O. Miranda,
  • Sonia Sayalero,
  • Esther Alza,
  • Patricia Llanes,
  • Miquel A. Pericàs

DOI
https://doi.org/10.3762/bjoc.7.172
Journal volume & issue
Vol. 7, no. 1
pp. 1486 – 1493

Abstract

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The application of polystyrene-immobilized proline-based catalysts in packed-bed reactors for the continuous-flow, direct, enantioselective α-aminoxylation of aldehydes is described. The system allows the easy preparation of a series of β-aminoxy alcohols (after a reductive workup) with excellent optical purity and with an effective catalyst loading of ca. 2.5% (four-fold reduction compared to the batch process) working at residence times of ca. 5 min.

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