80283-64-3Relevant articles and documents
Ammonium iodide-induced sulfonylation of alkenes with DMSO and water toward the synthesis of vinyl methyl sulfones
Gao, Xiaofang,Pan, Xiaojun,Gao, Jian,Huang, Huawen,Yuan, Gaoqing,Li, Yingwei
, p. 210 - 212 (2015)
A novel ammonium iodide-induced sulfonylation of alkenes with DMSO and water toward the synthesis of vinyl methyl sulfones is described. The process proceeded smoothly under metal-free conditions with high stereoselectivity and good functional group toler
Reactions of (Aryloxy)oxosulfonium Ylides with Carbonyl Compounds
Okuma, Kentaro,Nakanishi, Kazuto,Ohta, Hiroshi
, p. 1402 - 1407 (2007/10/02)
Reactions of (aryloxy)oxosulfonium salts with alkyllithium followed by the additon of carbonyl compounds gave β-aryloxy sulfones, β-aroyloxy sulfones, and α,β-unsaturated or β,γ-unsaturated sulfones in 1.4-17.9percent, 1.2-7.2percent, and 4.5-13.5percent yields, respectively.Ylides obtained by treatment of these sulfonium salts with n-BuLi reacted with carbonyl compounds to give betaines, which formed unusual four-membered cyclic alkoxyoxosulfonium salts.The aryloxy anions thus formed attacked β-carbons of these salts to afford β-aryloxy sulfones.The aroyloxy anion that might be formed by autoxidation also attacked β-carbons of these salts to afford β-aroyloxy sulfones.When these anions attacked the α- or γ-protones of these salts, unsaturated sulfones were obtained.This is the first example that the reaction of ylide with carbonyl compounds gave sulfone derivatives via four-membered cyclic alkoxyoxosulfonium salts that were produced by the intramolecular SN2 mechanism.The yields of unsaturated sulfones were raised up to 35-60percent by a one-pot reaction.
