An article Regioselective C-H Amidation of (Alkyl)arenes by Iron(II) Catalysis WOS:000465644300051 published article about N BOND FORMATION; NATURAL-PRODUCTS; COUPLING REACTIONS; DIRECT AMINATION; ARENES; AZIDES; CHLOROAMINES; ACTIVATION; PRECURSOR; MILD in [Ding, Yao; Zhang, Shen-Yuan; Fan, Shuai-Xin; Tian, Jie-Sheng; Loh, Teck-Peng] Nanjing Tech Univ NanjingTech, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, SCME, IAS, 30 South Puzhu Rd, Nanjing 211816, Jiangsu, Peoples R China; [Chen, Yu-Chen; Loh, Teck-Peng] Nanyang Technol Univ, Sch Phys & Math Sci, Div Chem & Biol Chem, Singapore 637371, Singapore; [Loh, Teck-Peng] Univ Sci & Technol China, Dept Chem, Hefei 230026, Anhui, Peoples R China in 2019, Cited 47. The Name is Diphenyl oxide. Through research, I have a further understanding and discovery of 101-84-8. Recommanded Product: 101-84-8
A nondirected amidation reaction of aromatic C-H bond was developed under iron(II) catalysis, using sulfonyl azides as the nitrogen source. The reaction displayed a broad substrate scope and good regioselectivities in the aspects of aromatic ring vs alkyl chain and different aromatic position of (alkyl)arenes. This method provided a new protocol for the synthesis of some aromatic amines, which were hard to achieve in a previous report.
Recommanded Product: 101-84-8. About Diphenyl oxide, If you have any questions, you can contact Ding, Y; Zhang, SY; Chen, YC; Fan, SX; Tian, JS; Loh, TP or concate me.
Reference:
Ether – Wikipedia,
,Ether | (C2H5)2O – PubChem