17118-70-6Relevant articles and documents
Facile 1,3-shift of chlorine in a chlorocarbonylketene
Finnerty, Justin,Andraos, John,Yamamoto, Yohsuke,Wong, Ming Wah,Wentrup, Curt
, p. 1701 - 1704 (1998)
Chlorocarbonyl(phenyl)ketene (2) undergoes a degenerate 1,3-shift of chlorine, as determined by 13C NMR spectroscopy. The two carbonyl signals (183 and 157 ppm) coalesce at -30°C, and from this as well as line-shape analysis, an activation barr
A one pot synthesis of 5-phenyl-1,3-dioxane-4,6-dione derivatives
Saidi,Shaterian,Sheibani
, p. 2345 - 2351 (2007/10/03)
A general procedure for synthesis of 5-phenyl-1,3-dioxane-4,6-dione derivatives is described. The synthesis involves the cycloaddition of (α- chlorocarbonyl)phenylketene with carbonyl compounds to generate the corresponding substituted 2-oxetanone's which is readily transformed to the final products in one step. The 1,3-dioxane-4,6-dione is a rigid cyclic structure, and can undergo easy hydrolysis.