Related Experiment Video
Updated: Jul 12, 2026

Enzymatic Cascade Reactions for the Synthesis of Chiral Amino Alcohols from L-lysine
Published on: February 16, 2018
Catalytic enantioselective hetero-Diels-Alder reactions of an azo compound
Masanori Kawasaki1, Hisashi Yamamoto
1Department of Chemistry, University of Chicago, 5735 South Ellis Avenue, Chicago, IL 60637, USA.
Abstract:
This communication describes studies in which an azo hetero-Diels-Alder adduct was furnished in high regio- and enantioselectivity using azopyridine as a reagent and silver as a catalyst. The obtained hetero-Diels-Alder adduct was easily converted to the corresponding chiral 1,4-diamino alcohol.
Related Concept Videos
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Crossed Aldol Reaction Using Strong Bases: Directed Aldol Reaction
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
Aldol Condensation with β-Diesters: Knoevenagel Condensation
Heterogeneous Catalysis

