91850-96-3Relevant articles and documents
Enantioselective additions of (trifluoromethyl)trimethylsilane to α-imino ketones derived from aryl glyoxals
Obijalska, Emilia,Mlostoń, Grzegorz,Six, Alice
, p. 2462 - 2465 (2013/07/05)
Chemoselective additions of (trifluoromethyl)trimethylsilane to α-imino ketones derived from aryl glyoxals in the presence of a catalytic amount of enantiomerically pure ammonium bromides, derived from Cinchona alkaloids and K2CO3 le
Reactions of α-imino ketones derived from arylglyoxals with (trifluoromethyl)trimethylsilane; A new route to β-amino-α- trifluoromethyl alcohols
Mloston, Grzegorz,Obijalska, Emilia,Tafelska-Kaczmarek, Agnieszka,Zaidlewicz, Marek
experimental part, p. 1289 - 1296 (2011/02/22)
The reactions of α-imino ketones, derived from arylglyoxals, with (trifluoromethyl)trimethylsilane (CF3SiMe3) in DME solution, in the presence of catalytic amount of CsF, at room temperature, yield O-silylated β-imino alcohols in the
Removal of Toluene-p-sulphonyl Groups from Sulphonamides. Part 4. Synthesis of Phenylglyoxal Imine Monomers
McKay, William R.,Proctor, George R.
, p. 2435 - 2442 (2007/10/02)
Syntheses and reactions of N-tosylphenacylamines with bases have been systematically examined.Monomeric C-methoxy-imines are available from some of these reactions.C-Methoxyphenacylarylamines, made by two routes, were converted into monomeric imines on treatment with noble-metal catalysts, The boron trifluoride-catalysed reactions of aryl aldehydes with sulphonamides provide a new and convenient route to N-sulphonylarylimines.