Some Condensations at the Methylene and Terminal Methyl Groups of Benzenesulfonylacetone Through its Mono-and Dipotassio Salts1, 2
WI O'Sullivan, DF Tavares…
Index: O'Sullivan,W.I. et al. Journal of the American Chemical Society, 1961 , vol. 83, p. 3453 - 3457
Full Text: HTML
Citation Number: 6
Abstract
Benzenesulfonylacetone was benzylated and benzoylated at its methylene group through its monopotassio salt to form the C-benzyl and 0-benzoyl derivatives, respectively. The benzyl derivative was coupled with benzenediazonium chloride to give an azo compound, whereas benzenesulfonylacetone was converted by this reagent to a phenylhydrazone. Benzenesulfonylacetone was benzylated and benzoylated at its terminal methyl group ...
Related Articles:
[Fargeas, Valerie; Baalouch, Myriam; Metay, Estelle; Baffreau, Jerome; Menard, Delphine; Gosselin, Pascal; Berge, Jean-Pascal; Barthomeuf, Chantal; Lebreton, Jacques Tetrahedron, 2004 , vol. 60, # 45 p. 10359 - 10364]
[Fargeas, Valerie; Baalouch, Myriam; Metay, Estelle; Baffreau, Jerome; Menard, Delphine; Gosselin, Pascal; Berge, Jean-Pascal; Barthomeuf, Chantal; Lebreton, Jacques Tetrahedron, 2004 , vol. 60, # 45 p. 10359 - 10364]
[Fargeas, Valerie; Baalouch, Myriam; Metay, Estelle; Baffreau, Jerome; Menard, Delphine; Gosselin, Pascal; Berge, Jean-Pascal; Barthomeuf, Chantal; Lebreton, Jacques Tetrahedron, 2004 , vol. 60, # 45 p. 10359 - 10364]