80223-59-2Relevant articles and documents
Sequential reduction and dehydration of phenacyl-(E)-styryl sulfones to unsymmetrical (E,E)-bis(styryl) sulfones
Mallireddigari, Muralidhar Reddy,Pallela, Venkat R.,Reddy, E. Premkumar,Reddy, M. V. Ramana
, p. 3639 - 3643 (2007/10/03)
β-Keto vinylic sulfones, the key building blocks for the synthesis of the title compounds, were prepared by two different routes. NaBH4 reduction of these compounds afforded β-hydroxy vinylic sulfones which were dehydrated with acetic anhydride
Reactions of 1,4-Pentadien-3-ones, 22. - Synthesis and Structure of the Epimers of 3,5-Diaryl-4-hydroxy-1,4-thiazinane 1,1-Dioxides
Yamamura, Hiroko,Kleffel, Dagmar,Blount, John F.,Hunkler, Dieter,Todaro, Louis J.,Otto, Hans-Hartwig
, p. 1013 - 1023 (2007/10/02)
Distyrylsulfones 1 react with the ambident nucleophile hydroxylamine only by double addition of nitrogen to give 4-hydroxy-1,4-thiazinane derivatives 3.In solution 3 consists of a temperature-dependent equilibrium mixture of two epimers.When heated or whe