An article Poly(ethylene glycol) dimethyl ether mediated oxidative scission of aromatic olefins to carbonyl compounds by molecular oxygen WOS:000641127700018 published article about GEM-DISUBSTITUTED ALKENES; C=C BOND-CLEAVAGE; C DOUBLE-BOND; SELECTIVE OXIDATION; EFFICIENT; HYDROGENATION; OZONOLYSIS; QUINOLINES; CATALYSTS; COMPLEX in [Yu, Tao; Guo, Mingqing; Wen, Simiaomiao; Zhao, Rongrong; Wang, Jinlong; Sun, Yanli; Liu, Qixing; Zhou, Haifeng] China Three Gorges Univ, Res Ctr Green Pharmaceut Technol & Proc, Hubei Key Lab Nat Prod Res & Dev, Coll Biol & Pharmaceut Sci, Yichang 443002, Peoples R China in 2021, Cited 51. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1. Name: Phenyl(pyridin-2-yl)methanone
A simple, and practical oxidative scission of aromatic olefins to carbonyl compounds using O-2 as the sole oxidant with poly(ethylene glycol) dimethyl ether as a benign solvent has been developed. A wide range of monosubstituted, gem-disubstituted, 1,2-disubstituted, trisubstituted and tetrasubstituted aromatic olefins was successfully converted into the corresponding aldehydes and ketones in excellent yields even with gram-scale reaction. Some control experiments were also conducted to support a possible reaction pathway.
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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem