132398-40-4Relevant articles and documents
O-Nitrophenyl sulfoxides: Efficient precursors for the mild preparation of alkenes
Lu, Xiao,Long, Timothy E.
supporting information; experimental part, p. 249 - 252 (2010/04/06)
(Chemical Equation Presented) o-Nitrophenyl sulfoxides were found to be efficient synthetic precursors of various alkene types. The elimination occurs in toluene and NaOAc to generate substituted and terminal alkenes. Alkene products were easily obtained in high purity due to the simultaneous precipitation of the o-nitrophenyl sulfenic acid byproduct. The methods described have practical applications for the preparation of unsaturated compounds under mild, thermolytic conditions. 2009 American Chemical Society.
Generation and intramolecular cyclization of α-sulfinyl and α-sulfonyl radicals
Ke, Bor-Wen,Lin, Chao-Hsiung,Tsai, Yeun-Min
, p. 7805 - 7826 (2007/10/03)
α-Phenylsulfinyl and α-Phenylsulfonyl radicals are generated by the reactions of α-chlorosulfoxides and α-chlorosulfones with tributyltin hydride, respectively. High reaction concentration (0.2 M) is required to ensure efficient generations of these radic