Related Articles:

Potent BRAF kinase inhibitors based on 2, 4, 5-trisubstituted imidazole with naphthyl and benzothiophene 4-substituents

[Niculescu-Duvaz, Dan; Niculescu-Duvaz, Ion; Suijkerbuijk, Bart M.J.M.; Menard, Delphine; Zambon, Alfonso; Davies, Lawrence; Pons, Jean-Francois; Whittaker, Steven; Marais, Richard; Springer, Caroline J. Bioorganic and Medicinal Chemistry, 2013 , vol. 21, # 5 p. 1284 - 1304]

Highly efficient synthesis of aryl and heteroaryl trifluoromethyl ketones via o-iodobenzoic acid (IBX)

[Cheng, Huicheng; Pei, Yu; Leng, Faqiang; Li, Jingya; Liang, Apeng; Zou, Dapeng; Wu, Yangjie; Wu, Yusheng Tetrahedron Letters, 2013 , vol. 54, # 33 p. 4483 - 4486]

Trifluoromethylation of Ketones and Aldehydes with Bu3SnCF3

[Motherwell, William B.; Storey, Lynda J. Journal of Fluorine Chemistry, 2005 , vol. 126, # 4 p. 491 - 498]

A sterically demanding organo-superbase avoids decomposition of a naked trifluoromethyl carbanion directly generated from fluoroform

[Kawai, Hiroyuki; Yuan, Zhe; Tokunaga, Etsuko; Shibata, Norio Organic and Biomolecular Chemistry, 2013 , vol. 11, # 9 p. 1446 - 1450]

Nucleophilic Trifluoromethylation of Carbonyl Compounds: Trifluoroacetaldehyde Hydrate as a Trifluoromethyl Source

[Surya Prakash; Zhang, Zhe; Wang, Fang; Munoz, Socrates; Olah, George A. Journal of Organic Chemistry, 2013 , vol. 78, # 7 p. 3300 - 3305]