Showing papers by "Glenn M. Sammis published in 2003"

Highly Enantioselective, Catalytic Conjugate Addition of Cyanide to α,β-Unsaturated Imides

Abstract: (Salen)Al−Cl complex 1a catalyzes the asymmetric conjugate addition of hydrogen cyanide to α,β-unsaturated imides in high yields and enantioselectivities. The cyanide adducts can readily be converted into a variety of useful chiral building blocks, including α-substituted-β-amino acids and β-substituted-γ-aminobutyric acids. Mechanistic data obtained thus far point to a cooperative bimetallic mechanism for nucleophile and electrophile activation.

Highly Enantioselective, Catalytic Conjugate Addition of Cyanide to α,β-Unsaturated Imides.

Abstract: (Salen)Al−Cl complex 1a catalyzes the asymmetric conjugate addition of hydrogen cyanide to α,β-unsaturated imides in high yields and enantioselectivities. The cyanide adducts can readily be converted into a variety of useful chiral building blocks, including α-substituted-β-amino acids and β-substituted-γ-aminobutyric acids. Mechanistic data obtained thus far point to a cooperative bimetallic mechanism for nucleophile and electrophile activation.