Related Experiment Video
Updated: Feb 12, 2026

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
Published on: October 18, 2019
Prolinate Salt as a Catalyst in the syn-Selective, Asymmetric Mannich Reaction of Alkynyl Imine
Yujiro Hayashi1, Tatsuya Yamazaki2, Genki Kawauchi1
1Department of Chemistry, Graduate School of Science , Tohoku University , 6-3 Aramaki-Aza , Aoba, Aoba-ku, Sendai , Miyagi 980-8578 , Japan.
Abstract:
Prolinate salt is an efficient catalyst in the Mannich reaction of alkynyl imine and aldehyde, to afford synthetically useful chiral propargyl amine derivatives with excellent syn-selectivity and nearly perfect control of the absolute configuration. The counterion of the prolinate salt does not affect the enantioselectivity. This is a rare example, in which proline alkali metals, alkaline-earth metals, or ammonium salt show higher reactivity and better stereoselectivity than the parent proline.
Related Concept Videos
Determining the pH of Salt Solutions
Responses to Salt Stress
Rotation of Asymmetric Top
The relationship between the angular momentum of any rigid body and its angular velocity, both of which are vectors, involves the moment of inertia. The moment of inertia is a scalar quantity only for spherically symmetric...
Reaction Rate
The mathematical representation of the change in the concentration of reactants and products, over time, is the rate...
Asymmetric Lipid Bilayer
Precipitation Reactions

