13031-45-3Relevant articles and documents
Ligand-Promoted Palladium-Catalyzed C?H Acetoxylation of Simple Arenes
Valderas, Carolina,Naksomboon, Kananat,Fernández-Ibá?ez, M. ángeles
, p. 3213 - 3217 (2016/10/24)
The palladium-catalyzed C?H oxidation of simple arenes is an attractive strategy to obtain phenols, which have many applications in the fine chemicals industry. Although some advances have been made in this research area, low reactivity and selectivity are, in general, observed. This report describes a new catalytic system for the efficient C?H acetoxylation of simple arenes based on Pd(OAc)2 and a pyridinecarboxylic acid ligand.
Remarkably high reactivity of Pd(OAc)2/pyridine catalysts: Nondirected C-H oxygenation of arenes
Emmert, Marion H.,Cook, Amanda K.,Xie, Yushu J.,Sanford, Melanie S.
supporting information; experimental part, p. 9409 - 9412 (2011/11/07)
Less is more: The rational optimization and general applicability of the catalytic system Pd(OAc)2/pyridine is described (see scheme). The catalyst shows excellent reactivity in the C-H oxygenation of simple aromatic substrates. The Pd/pyridine ratio is critical as the use of one equivalent of pyridine per Pd center leads to dramatic enhancements in both reactivity and site selectivity in comparison to Pd(OAc)2 alone.
Air-stable titanocene bis(perfluorooctanesulfonate) as a new catalyst for acylation of alcohols, phenols, thiols, and amines under solvent-free condition
Qiu, Renhua,Zhang, Guoping,Ren, Xiaofang,Xu, Xinhua,Yang, Ronghua,Luo, Shenglian,Yin, Shuangfeng
experimental part, p. 1182 - 1188 (2010/06/13)
Air-stable titanocene bis(perfluorooctanesulfonate) [Cp2Ti(OSO2C8F17)2] that shows high Lewis acidity was prepared from Cp2TiCl2 and AgOSO2C8F17. The compound was characterized by different techniques, and examined as a catalyst for acylation reactions. It was found that using equimolar acetic anhydride as acetylating agent and under solvent-free condition, Cp2Ti(OSO2C8F17)2 exhibits high activity and selectivity in the acetylation of various alcohols, phenols, thiols, and amines. Also, good catalytic efficiency is observed in the acylation of 2-phenylethanol across various acylating reagents. The catalyst can be reused without loss of activity in a test of ten cycles. The Cp2Ti(OSO2C8F17)2 catalyst affords a simple, efficient and general method for the acylation of alcohols, phenols, thiols, and amines.