Related Experiment Video
Updated: May 30, 2025

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
Recent advances in green multi-component reactions for heterocyclic compound construction
Xinling Shen1, Gang Hong1,2, Limin Wang1
1Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. China. wanglimin@ecust.edu.cn.
Abstract:
Multi-component reactions (MCRs) are processes in which three or more reactants are introduced into one pot to obtain the final product with high atom efficiency, and in recent years, these have become a key strategy for advancing more sustainable processes in modern synthetic communities and the pharmaceutical industry. Meanwhile, minimizing the use of solvents, catalysts, time, reagents, and waste is essential during green chemical synthesis to reduce cost and environmental impact. Heterocycles are ubiquitous and have thus prompted the development of numerous methods for their synthesis. Among various strategies, MCRs represent one of the most promising routes for the synthesis of heterocyclic moieties such as quinolines, quinazolines, pyrimidines and imidazoles, which are widely recognized in nature and clinical evaluation. To promote greener syntheses, a significant body of literature detailing the synthesis of these biologically important compounds via environmentally friendly MCRs has emerged. This review focused on the recent advances in the green approach to preparing heterocyclic compounds via MCRs. These green approaches included photoredox catalysis, electrochemical activation, catalyst-free methods, and the use of water as the sole green solvent, reported between 2018 and 2024, highlighting their strengths and limitations. The synthesis of different types of heterocycles via green MCRs was covered. The substrate scope, reaction conditions, yields and mechanisms were also examined and discussed.
Related Concept Videos
Cycloaddition Reactions: Overview
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
Pericyclic Reactions: Introduction
Pericyclic reactions can be classified into three categories: electrocyclic reactions, cycloaddition reactions, and sigmatropic rearrangements. Electrocyclic reactions and sigmatropic...
Thermal and Photochemical Electrocyclic Reactions: Overview
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Cycloaddition Reactions: MO Requirements for Thermal Activation

![Solid-phase Synthesis of [4.4] Spirocyclic Oximes](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F58508.jpg&w=3840&q=50)