65350-61-0Relevant academic research and scientific papers
Synthesis of divinylsulfides
Paradies, Jan
experimental part, p. 947 - 952 (2010/04/30)
Arylacetylenes react with sodium sulfide in the presence of water to yield divinylsulfides. The reaction proceeds in good to excellent yield for both electron-neutral and electron-deficient aromatic systems; for electron-rich aryls, longer reaction times are necessary. The sulfides represent useful substrates for further transformations, for example, oxidation to the corresponding divinylsulfoxides and divinylsulfones. Three selected divinylsulfide derivatives were oxidized selectively to the corresponding sulfoxides or sulfones. Georg Thieme Verlag Stuttgart ? New York.
THIOGLYCOLATES IN THE SYNTHESIS OF BIS(STYRYL)SULFONES
Reddy, M. V. Ramana,Reddy, S.,Reddy, D. Bhaskar,Padmavathi, V.
, p. 1101 - 1108 (2007/10/02)
E,Z-Bis(styryl)sulfones (6), have been prepared by the Knoevenagel condensation of Z-styrylsulfonylacetic acid (5) with araldehydes.The compound 5 was prepared by a novel route using thioglycolates and phenylacetylene.The configuration of 6 has been assig
