In 2020.0 EUR J ORG CHEM published article about SELECTIVE SYNTHESIS; PENTAARYLPYRIDINES; ARYLPYRIDINES; CONSTRUCTION; CONDENSATION; DERIVATIVES; ENAMINES; KINETICS; BINDING in [Arita, Mao; Yokoyama, Soichi; Asahara, Haruyasu; Nishiwaki, Nagatoshi] Kochi Univ Technol, Sch Environm Sci & Engn, Kami Kochi 7828502, Japan; [Yokoyama, Soichi; Asahara, Haruyasu; Nishiwaki, Nagatoshi] Kochi Univ Technol, Res Ctr Mat Sci & Engn, Kami Kochi 7828502, Japan; [Asahara, Haruyasu] Osaka Univ, Grad Sch Pharmaceut Sci, Yamadaoka 1-6, Suita, Osaka 5650871, Japan in 2020.0, Cited 47.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Recommanded Product: 1-(4-Nitrophenyl)ethanone
Condensation of beta-(2-pyridyl)enamine and alpha,beta-unsaturated ketone in the presence of FeCl3 under air afforded highly substituted pyridines. In this transformation, FeCl3 acted as not only an acid catalyst but also an oxidant for the intermediate dihydropyridine. The substituents could be easily modified by altering the substrates to obtain tri- and tetraarylpyridines including bipyridines and terpyridine. Synthesis of differently substituted pentaarylpyridines was consequently achieved via only three steps from commercially available reagents with simple experimental manipulations.
Recommanded Product: 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Arita, M; Yokoyama, S; Asahara, H; Nishiwaki, N or concate me.
Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem