2495-39-8Relevant articles and documents
Synthesis of sodium allyl sulfonate in an aqueous medium by micellar catalysis with methoxy polyethylene glycol methacrylates
Orekhov,Kazantsev,Sivokhin,Khokhlova
, p. 881 - 886 (2014)
Micellar catalysis with various polyoxyethylated compounds was used to synthesize sodium allyl sulfonate by the reaction of allyl chloride with an aqueous solution of sodium sulfite. It was shown that methoxy polyethylene glycol methacrylates and water soluble polymers based on these compounds are surfactants and can be used to intensify the synthesis of sodium allyl sulfonate, which is of interest in the case of its subsequent application to obtain copolymers with methoxy polyethylene glycol methacrylates.
Ring closing metathesis and metal-catalyzed cyclopropanation for the preparation of sultone derivatives
Ali, Korany A.,Metz, Peter
, p. 19 - 29 (2019/04/17)
Ring closing metathesis (RCM) using Grubbs catalyst 2nd generation as a catalyst was applied to prepare series of novel unsaturated sultones with high yields. Many attempts, were applied for the cyclopropanation of the allylic sultones by Simmon-smith cyclopropanation using diethyl zinc/diiodomethane or Zn-Cu/diiodomethane but in each case the corresponding cyclic adduct was not formed. A novel palladium or preferably rhodium-catalyzed cyclopropanation of unsaturated sultones with ethyl diazoacetate was achieved by the transition metal-catalyzed transfer of a CH-CO2Et unit. The reaction was applied by a portion-wise addition of ethyl diazoacetate over 6h to a mixture of the sultones and palladium(II) acetate or rhodium(II) acetate dimer under low temperature (0-20 o C). The desired products of the cyclopropanation were achieved in each case, as a single diastereomer with 33- 37% yield in the allylic sultones and 10% for vinylic sultone.
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