An article Scandium(III) Triflate Catalyzed Direct Synthesis of N-Unprotected Ketimines WOS:000506088700025 published article about MANNICH-TYPE REACTIONS; BOND FORMATION; ARYL HALIDES; ALPHA-AMINO; ASYMMETRIC HYDROGENATION; BENZOPHENONE IMINE; DIRECT ACCESS; SCHIFF-BASES; DERIVATIVES; ACTIVATION in [Kondo, Yuta; Kadota, Tetsuya; Hirazawa, Yoshinobu; Morisaki, Kazuhiro; Morimoto, Hiroyuki; Ohshima, Takashi] Kyushu Univ, Grad Sch Pharmaceut Sci, Higashi Ku, Maidashi 3-1-1, Fukuoka 8128582, Japan; [Morisaki, Kazuhiro] Kyoto Univ, Inst Chem Res, Kyoto 6110011, Japan in 2020.0, Cited 67.0. Safety of Phenyl(pyridin-2-yl)methanone. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1
N-Unprotected ketimines are useful substrates and intermediates for synthesizing valuable nitrogen-containing compounds, but their potential applicability is limited by the available synthetic methods. To address this issue, we report a scandium(III) triflate catalyzed direct synthesis of N-unprotected ketimines. Using commercially available reagents and Lewis acid catalysts, ketones were directly transformed into the corresponding N-unprotected ketimines in high yields with broad functional group tolerance, even in multigram scales. The reactions were readily applicable for one-pot synthesis of important compounds such as a glycine Schiff base without isolation of N-unprotected ketimine intermediates. Preliminary mechanistic studies to clarify the reaction mechanism are also described.
Safety of Phenyl(pyridin-2-yl)methanone. About Phenyl(pyridin-2-yl)methanone, If you have any questions, you can contact Kondo, Y; Kadota, T; Hirazawa, Y; Morisaki, K; Morimoto, H; Ohshima, T or concate me.
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem