Saltar al contenido
Merck
  • Small amounts of achiral beta-amino alcohols reverse the enantioselectivity of chiral catalysts in cooperative asymmetric autocatalysis.

Small amounts of achiral beta-amino alcohols reverse the enantioselectivity of chiral catalysts in cooperative asymmetric autocatalysis.

Journal of the American Chemical Society (2005-09-01)
François Lutz, Takashi Igarashi, Tsuneomi Kawasaki, Kenso Soai
RESUMEN

An asymmetric autocatalytic reaction has been catalyzed by a mixture of chiral and achiral beta-amino alcohols. The absolute configuration of the highly enantioenriched obtained product (>98% ee) was shown to depend not only on the absolute configuration of the chiral catalyst but also on the structure and the amount of achiral catalyst. Even in default versus the chiral catalyst, achiral catalysts were shown to be able to reverse the enantioselectivity of the reaction.

MATERIALES
Referencia del producto
Marca
Descripción del producto

Sigma-Aldrich
1-(2-Hydroxyethyl)piperidine, ReagentPlus®, 99%