Direkt zum Inhalt
Merck
  • Direct asymmetric iodination of aldehydes using an axially chiral bifunctional amino alcohol catalyst.

Direct asymmetric iodination of aldehydes using an axially chiral bifunctional amino alcohol catalyst.

Journal of the American Chemical Society (2008-03-07)
Taichi Kano, Mitsuhiro Ueda, Keiji Maruoka
ZUSAMMENFASSUNG

A direct asymmetric iodination reaction of aldehydes with NIS was found to be catalyzed by the novel axially chiral bifunctional amino alcohol (S)-1d. This method represents the rare example of the catalytic and highly enantioselective synthesis of optically active alpha-iodoaldehydes.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
N-Iodsuccinimid, 95%