Related Experiment Video
Updated: Aug 19, 2026
![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)
Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions
Published on: July 17, 2020
9,10-Phenanthrenequinone (PQ): a versatile catalyst in organic synthesis
Xian-Bing Luo1,2, Fei-Fei Xu1, Zhifang Li2
1Advanced Research Institute and School of Pharmaceutical Sciences, Taizhou University, Jiaojiang, Zhejiang 318000, P. R. China. zhongwei.hou@tzc.edu.cn.
None:
Aromatic carbonyl compounds have garnered significant attention as photocatalysts for diverse chemical transformations. Among these, 9,10-phenanthrenequinone (PQ) is widely used in organic synthesis due to its low cost, ease of availability, and distinctive physical and chemical properties. The excited state of PQ facilitates substrate activation through mechanisms such as single electron transfer (SET) and hydrogen atom transfer (HAT). Additionally, PQ can catalyze the dehalogenation of α-bromoanilides and serves as a ligand in organic synthesis. Recently, PQ-catalyzed organic transformations have emerged as a potent strategy for synthesizing a wide array of organic molecules. This review aims to concisely summarize the latest advancements in utilizing PQ as a versatile catalyst for organic reactions, while also exploring the reaction design, mechanistic insights, and future development prospects of these methodologies.
Related Concept Videos
Oxidation of Phenols to Quinones
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox property is crucial in...
Radical Chain-Growth Polymerization: Overview
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Cycloaddition Reactions: MO Requirements for Photochemical Activation
ortho–para-Directing Activators: –CH3, –OH, –⁠NH2, –OCH3
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
![[(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F59739.jpg&w=3840&q=50)
