An article Fe-S Catalyst Generated In Situ from Fe(III)- and S-3(center dot-)-Promoted Aerobic Oxidation of Terminal Alkenes WOS:000664333200039 published article about TRISULFUR RADICAL-ANION; MOLECULAR-OXYGEN; CLEAVAGE; IRON; SULFUR; OLEFINS; HYDROXYLATION; CHEMISTRY; BONDS; ACID in [Ai, Jing-Jing; Liu, Bei-Bei; Li, Jian; Wang, Fei; Huang, Cheng-Mi; Wang, Shun-Yi] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Key Lab Organ Synth Jiangsu Prov, Suzhou 215123, Peoples R China; [Ai, Jing-Jing; Liu, Bei-Bei; Li, Jian; Wang, Fei; Huang, Cheng-Mi; Wang, Shun-Yi] Soochow Univ, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Suzhou 215123, Peoples R China; [Rao, Weidong] Nanjing Forestry Univ, Coll Chem Engn, Key Lab Biomass Based Green Fuels & Chem, Nanjing 210037, Peoples R China in 2021, Cited 47. Formula: C12H9NO. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1
An iron-sulfur complex formed by the simple mixture of FeCl3 with S-3(center dot-) generated in situ from K2S is developed and applied to selective aerobic oxidation of terminal alkenes. The reaction was carried out under an atmosphere of O-2 (balloon) and could proceed on a gram scale, expanding the application of S-3(center dot-) in organic synthesis. This study also encourages us to explore the application of an Fe-S catalyst in organic reactions.
Formula: C12H9NO. Bye, fridends, I hope you can learn more about C12H9NO, If you have any questions, you can browse other blog as well. See you lster.
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem