Related Experiment Video
Updated: May 10, 2025

Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
Visible Light-Induced C─C Bond Cleavage for the Construction of Ketone Using Molecular Oxygen
Bin Sun1,2, Haijing Song1, Siyu Pan1
1College of Pharmaceutical Sciences, Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
Abstract:
The selective cleavage of carbon-carbon bonds by photocatalysis with the participation of oxygen for ketone synthesis and drug derivatization is reported. In this oxidation-based ketone formation reaction, molecular oxygen complexes with the substrate, which is subsequently photoexcited to generate a charge transfer (CT) state. This CT state facilitates energy transfer with molecular oxygen, producing singlet oxygen, which facilitates hydrogen atom process and promotes the subsequent cleavage of the carbon-carbon bond, ultimately leading to the formation of aryl ketone compounds. 48 aryl ketone compounds and pharmaceutical derivatives were synthesized using this method. A notable feature of this reaction is its catalyst-free, additive-free, and transition metals-free nature combined with green, mild, and environmentally friendly reaction conditions enabling high yields.
More Related Videos
Related Concept Videos
Alkynes to Carboxylic Acids: Oxidative Cleavage
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Radical Formation: Homolysis
IR and UV–Vis Spectroscopy of Aldehydes and Ketones
Preparation of Aldehydes and Ketones from Alcohols, Alkenes, and Alkynes
C–C Bond Cleavage: Retro-Aldol Reaction
In the first step, as depicted in Figure 1, the base deprotonates the β-hydroxy ketone at the hydroxyl group to form an alkoxide ion.

