Related Experiment Video
Updated: Mar 20, 2026

Optimization of the Ugi Reaction Using Parallel Synthesis and Automated Liquid Handling
Published on: November 11, 2008
Revisited Mechanistic Implications of the Joullié-Ugi Three-Component Reaction
Akira Katsuyama1, Akira Matsuda1,2, Satoshi Ichikawa1,2
1Faculty of Pharmaceutical Sciences, Hokkaido University , Kita-12, Nishi-6, Kita-ku, Sapporo 060-0812, Japan.
Abstract:
The effect of the solvent on the diastereoselectivity of the Joullié-Ugi three-component reaction (JU-3CR) using an α-substituted five-membered cyclic imine is revisited. The cis and trans isomers were generated in toluene and HFIP, respectively. Hammett analysis of the JU-3CR suggests the presence of two reaction mechanisms.
Related Concept Videos
Reaction Mechanisms: Rate-limiting Step Approximation
Multi-Step Reactions
Woodward–Hoffmann Selection Rules and Microscopic Reversibility
Reaction Mechanisms
For instance, the decomposition of ozone appears to follow a mechanism with two steps:
Diels–Alder vs Retro-Diels–Alder Reaction: Thermodynamic Factors
Coupled Reactions
Energy in adenosine triphosphate or ATP molecules is easily accessible to do work. ATP powers the majority of energy-requiring cellular reactions....

