An article Rhodium-Catalyzed Pyridine N-Oxide Assisted Suzuki-Miyaura Coupling Reaction via C(O)-C Bond Activation WOS:000502163300105 published article about C-C BOND; CARBON-CARBON BONDS; CONJUGATED YNONES; ARYL KETONES; CLEAVAGE; PALLADIUM; DECARBONYLATION; REARRANGEMENT; FUNCTIONALIZATION; CARBOACYLATION in [Zhong, Jing; Long, Yang; Yan, Xufei; He, Shiyu; Ye, Runyou; Xiang, Haifeng; Zhou, Xiangge] Sichuan Univ, Coll Chem, 29 Wangjiang Rd, Chengdu 610064, Peoples R China in 2019, Cited 75. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1. Safety of Phenyl(pyridin-2-yl)methanone
A rhodium-catalyzed Suzuki-Miyaura coupling reaction via C(O)-C bond activation to form 2-benzoylpyridine N-oxide derivatives is reported. Both the C(O)-C(sp(2)) and C(O)-C(sp(3)) bond could be activated during the reaction with yields up to 92%. The N-oxide moiety could be employed as a traceless directing group, leading to free pyridine ketones.
Welcome to talk about 91-02-1, If you have any questions, you can contact Zhong, J; Long, Y; Yan, XF; He, SY; Ye, RY; Xiang, HF; Zhou, XG or send Email.. Safety of Phenyl(pyridin-2-yl)methanone
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem