158588-52-4Relevant academic research and scientific papers
A convenient access to β-iodo sulfone by the iodine-mediated iodosulfonylation of alkenes
Sun, Kai,Lv, Yunhe,Zhu, Zhonghong,Jiang, Yongqing,Qi, Jiejie,Wu, Hankui,Zhang, Zhiguo,Zhang, Guisheng,Wang, Xin
, p. 50701 - 50704 (2015)
A novel iodine-mediated intermolecular iodosulfonylation reaction of alkenes for dual C-S and C-I bond formation is described. A series of alkenes could be selectively converted into the corresponding β-iodo sulfones, which are versatile building blocks in organic synthesis and medicinal chemistry. Molecular iodine was the iodine source in this reaction.
The Importance of Polar, Resonance, Steric and Solvent Effects in the Addition of Sulfonyl Radicals to Alkenes
Correa, Carlos M. M. da Silva,Fleming, M. Daniela C. M.,Oliveira, M. Augusta B. C. S.,Garrido, Ermelinda M. J.
, p. 1993 - 2000 (2007/10/02)
The radical chain addition of tosyl iodide to some alkenes has been studied.The reaction was carried out at room temperature under visible light, giving the usual high yields of β-iodo sulfones.These adducts were transformed into the corresponding unsatur
