68116-50-7Relevant 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.
Synthesis of distyryl sulphides, sulphoxides and sulphones by Horner-Wittig reaction in two-phase system
Mikolajczyk, Marian,Popielarczyk, Miroslaw,Grzejszczak, Slawomir
, p. 369 - 374 (2007/10/02)
A convenient method is described for the formation of distyryl sulphides, sulphoxides and sulphones.Thus, Horner-Wittig reaction in two-phase system of the corresponding phosphonates with aromatic aldehydes affords the desired α, β unsaturated sulphur com
