Pd-catalyzed oxidative acylation of 2-phenoxypyridines with alcohols via C-H bond activation was written by Kim, Minyoung;Sharma, Satyasheel;Park, Jihye;Kim, Mirim;Choi, Yeonhee;Jeon, Yukyoung;Kwak, Jong Hwan;Kim, In Su. And the article was included in Tetrahedron in 2013.Application of 4783-68-0 This article mentions the following:
A palladium-catalyzed oxidative acylation of 2-phenoxypyridines with benzylic and aliphatic alcs. via C-H bond activation is described. This protocol represents direct access to biol. active ortho-acylphenol derivatives, and provides new opportunities to use readily available alcs. as starting materials for catalytic acylation reactions. In the experiment, the researchers used many compounds, for example, 2-Phenoxypyridine (cas: 4783-68-0Application of 4783-68-0).
2-Phenoxypyridine (cas: 4783-68-0) belongs to pyridine derivatives. Pyridine has a conjugated system of six π electrons that are delocalized over the ring. The molecule is planar and, thus, follows the Hückel criteria for aromatic systems. Several pyridine derivatives play important roles in biological systems. While its biosynthesis is not fully understood, nicotinic acid (vitamin B3) occurs in some bacteria, fungi, and mammals.Application of 4783-68-0