Related Experiment Video
Updated: Jan 7, 2026

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
Cooperative triple catalysis for complex molecule construction and late-stage functionalization
1Department of Chemistry, National Institute of Technology Puducherry, Karaikal-609609, Puducherry, India. dhaya.chem@nitpy.ac.in.
Abstract:
The recent development of modern catalysis has transformed synthetic chemistry by enabling highly efficient, selective, and sustainable C-C, C-N, C-O, and C-HA bond-forming processes. Among these innovations, triple catalysis the synergistic merger of three distinct catalytic cycles has emerged as a powerful strategy for addressing long-standing challenges in reactivity and chemo, regio and enantioselectivity. By merging photoredox catalysis, transition-metal catalysis, organocatalysis, or hydrogen atom transfer (HAT) cycles within a single reaction process, triple catalysis permits rapid access to previously unattainable transformations under mild or sustainable conditions. Such cooperative catalytic systems not only expand the chemical space by enabling unconventional bond constructions but also significantly improve reaction efficiency, broader substrate scope, and sensitive functional-group tolerance. This review provides a comprehensive overview of the design catalysts, mechanistic information, new molecule constructions and synthetic applications of the triple catalytic framework. This work covered recent advances in cross-coupling reactions, C-H functionalization, asymmetric synthesis, complex molecule construction, and late-stage functionalization of drugs and natural products. Triple catalysis represents a frontier strategy that demonstrates how cooperative catalytic systems can reshape synthetic methodologies and drive the next generation of drug discovery and materials science developments.
More Related Videos
10:17Efficient Construction of Drug-like Bispirocyclic Scaffolds Via Organocatalytic Cycloadditions of α-Imino γ-Lactones and Alkylidene Pyrazolones
Published on: February 7, 2019
07:50Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
Published on: May 26, 2019
Related Concept Videos
Cycloaddition Reactions: MO Requirements for Photochemical Activation
Cycloaddition Reactions: Overview
Cycloaddition Reactions: MO Requirements for Thermal Activation
Catalysis
Phase II Conjugation Reactions: Overview
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...