Pd(II)-catalyzed oxidative alkoxycarbonylation of 2-phenoxypyridine derivatives with CO and alcohols was written by Liu, Bin;Jiang, Huai-Zhi;Shi, Bing-Feng. And the article was included in Organic & Biomolecular Chemistry in 2014.Recommanded Product: 2-Phenoxypyridine This article mentions the following:
A Pd(II)-catalyzed oxidative alkoxycarbonylation of phenol derivatives with atm. pressure of CO-O2 and alcs. was achieved. The reaction provided an efficient strategy for the synthesis of carboxylic esters and can be applied to the late-stage modification of complex mols. In the experiment, the researchers used many compounds, for example, 2-Phenoxypyridine (cas: 4783-68-0Recommanded Product: 2-Phenoxypyridine).
2-Phenoxypyridine (cas: 4783-68-0) belongs to pyridine derivatives. Pyridine has a dipole moment and a weaker resonant stabilization than benzene (resonance energy 117 kJ·mol−1 in pyridine vs. 150 kJ·mol−1 in benzene). Pyridine, its benzo and pyridine-based compounds play diverse roles in organic chemistry. Pyridine-based materials are valued for their optical and physical properties as well as their medical potential. Recommanded Product: 2-Phenoxypyridine