113273-51-1Relevant articles and documents
Reductive Addition of Alkyl Radical to Phenyl Vinyl Sulfone
Togo, Hideo,Aoki, Masahiko,Yokoyama, Masataka
, p. 2169 - 2172 (1992)
Radicals generated from (diacyloxyiodo)benzene readily added to phenyl vinyl sulfone to give 2-alkylethyl phenyl sulfone in the presence of a hydrogen donor such as 1,4-cyclohexadiene, 1,3-dioxolane, or triethylsilane.Among these donors, 1,4-cyclohexadien
Reductive Addition to Electron-deficient Olefins with Trivalent Iodine Compounds
Togo, Hideo,Aoki, Masahiko,Yokoyama, Masataka
, p. 8241 - 8256 (2007/10/02)
(Diacyloxyiodo)arene was treated with electron-deficient olefins in the presence of hydrogen donor such as 1,4-cyclohexadiene to give the reductive addition products via alkyl radical through the radical decarboxylative pathway in good yields.Moreover, this system was able to generate either alkoxycarbonyl radicals or alkyl radicals with benzene, which was prepared from alcohol, oxalyl chloride, and (diacetoxyiodo)benzene via two steps, depending on reaction conditions.These radicals were also utilized for C-C bond formation with electron-deficient olefins.