55759-55-2Relevant academic research and scientific papers
The Wittig Reaction of some Fluorinated Amide Derivatives
Latham, Elliot J.,Murphy, Steven M.,Stanforth, Stephen P.
, p. 3395 - 3396 (1994)
Carboethoxymethylenetriphenylphosphorane 1 reacted with fluorinated amides 4,6,8 and 15 yielding products 12, 13, 14 and 3 respectively.
α- or β-Trifluoromethyl epoxysulfones: new C3 reagents for heterocyclisation
Laduron, Frederic,Janousek, Zdenek,Viehe, Heinz, G.
, p. 83 - 86 (2007/10/02)
The syntheses of α- and β-trifluoromethyl epoxysulfones 1 and 2 are described.Compound 1 reacts with nucleophiles and bis-nucleophiles to furnish trifluoromethyl ketones and trifluoromethyl heterocycles in good yield, while its isomer 2 leads to the opposite thiazole regioisomers with thioamides. - Keywords: Trifluoromethyl epoxysulfones; Heterocyclisation; Regioisomers; NMR spectroscopy; IR spectroscopy
Synthesis and reactions of [1-(trialkylsilyl)alkylidene]triphenylphosphoranes
Bestmann,Bomhard,Dostalek,Pichl,Riemer,Zimmermann
, p. 787 - 792 (2007/10/02)
Alkylidenetriphenylphosphoranes 1 react with trialkyl halosilanes 2 to afford silylated alkylidenephosphoranes 5, which can be converted to acylated alkylidenephosphoranes 8 and 10 by trimethylsilyl carboxylates 6 or carboxylic anhydrides 10. Bis(acylalkylidenephosphoranes) 13-15 are available from 5 and bis(trimethylsilyl) dicarboxylates 12 or cyclic or polymeric anhydrides 16, 17.
