Catalysts for asymmetric addition of organozinc reagents to aldehydes and method for preparation
AssigneeDuPont Pharmaceuticals Company
InventorWilliam A. Nugent
Life of this patent
Estimating the term…
Abstract
Novel chiral aminoalcohol catalysts and methods for their preparation are provided. The first catalyst is prepared via selective hydrogenation of one of two benzene rings in a precursor. The aminoalcohol promotes the asymmetric addition of organozinc reagents to aldehydes to afford optically active alcohols or their esters. The second catalyst is prepared by selective dialkylation of 3-exo-aminoisoborneol with a 2-haloethyl ether. The aminoalcohol promotes the addition of organozinc reagents to aliphatic aldehydes containing a β-branch with greatly enhanced enantioselectivity relative to DAIB.
Claims7
An erythro β-aminoalcohol compound of the formula:
A process to prepare an erythro-β-aminoalcohol compound of Formula 1
- comprising selectively hydrogenating an erythro-β-aminoalcohol of Formula 2
- to form the erythro-β-aminoalcohol of Formula 1.
Dependencies are inferred from the claim text.