6178-56-9Relevant academic research and scientific papers
Synthesis of β-hydroxy sulfones via opening of hydrophilic epoxides with zinc sulfinates in aqueous media
Chumachenko, Nataliya,Sampson, Paul
, p. 4540 - 4548 (2007/10/03)
Reaction of hydrophilic epoxides (ethylene oxide and propylene oxide) with readily accessible zinc sulfinates in aqueous solution under essentially neutral conditions afforded β-hydroxy sulfones in good yields. This method avoids the need for organic solvents and produces ZnO as the only major reaction byproduct. 2-(Methylsulfonyl)ethanol, a common reagent for the protection of various functional groups, was obtained by this methodology from ethylene oxide in 78% yield. Reaction of various simple zinc alkane- and benzenesulfinates with propylene oxide proceeded regioselectively in 63-67% yield. The corresponding opening of these epoxides with zinc 1,3-butadiene-1-sulfinate afforded 1-butadienyl β-hydroxyalkyl sulfones in 30% yield. Mechanistic studies revealed that the yields of these products were limited by their consumption in competing intra- and intermolecular Michael addition processes.
Sulfone Directed Rhodium Catalysed Hydroboration: Regiochemistry in Acyclic System
Hou, Xue-Long,Hong, Dao-Guang,Rong, Guo-Bin,Guo, Yang-Long,Dai, Li-Xin
, p. 8513 - 8516 (2007/10/02)
Rhodium catalysed hydroboration of allyl sulfones gave rise to Markownikoff product with high regioselectivity.
