1262-57-3Relevant articles and documents
Preparation, reactivities, and NMR spectra of pentafluorophenyltin derivatives
Chen, Jian-Xie,Sakamoto, Katsumasa,Orita, Akihiro,Otera, Junzo
, p. 58 - 65 (2007/10/03)
A variety of pentafluorophenyltin compounds were prepared and their chemical properties were examined. These compounds effectively catalyzed Mukaiyama-aldol reaction of ketene silyl acetal in sharp contrast to the inertness of normal alkyltin halides like Bu2SnCl2. The increased Lewis acidity of the pentafluorophenyltin halides was proved by 119Sn- and 13C-NMR spectra. On the other hand, the pentafluorophenyl group reduced the reactivities of tin towards both nucleophiles and electrophiles. 19F-NMR spectroscopy was invoked to elucidate this anomaly.