An article Acyl Radicals from alpha-Keto Acids Using a Carbonyl Photocatalyst: Photoredox-Catalyzed Synthesis of Ketones WOS:000569377600028 published article about C-H BONDS; OXOCARBOXYLIC ACIDS; MERGING PHOTOREDOX; ELECTRON-TRANSFER; CARBOXYLIC-ACIDS; ARYL HALIDES; LIGHT; METAL; ACYLATION; ALKENES in [Zhu, Da-Liang; Wu, Qi; Wang, Hao; Ren, Zhi-Gang; Li, Hong-Xi] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China; [Young, David James] Charles Darwin Univ, Coll Engn Informat Technol & Environm, Darwin, NT 0909, Australia in 2020.0, Cited 65.0. The Name is Chalcone. Through research, I have a further understanding and discovery of 94-41-7. HPLC of Formula: C15H12O
Acyl radicals have been generated from alpha-keto acids using inexpensive and commercially available 2-chloro-thioxanthen-9-one as the photoredox catalyst under visible light illumination. These reactive species added to olefins or coupled with aryl halides via a bipyridyl-stabilized Ni(II) catalyst, enabling easy access to a diverse range of ketones. This reliable, atom-economical, and eco-friendly protocol is compatible with a wide range of functional groups.
About Chalcone, If you have any questions, you can contact Zhu, DL; Wu, Q; Young, DJ; Wang, H; Ren, ZG; Li, HX or concate me.. HPLC of Formula: C15H12O
Reference:
Thiazolidine – Wikipedia,
,Thiazolidine – ScienceDirect.com