个性化文献订阅>期刊> Synthesis
 

Oligomeric Iodosylbenzene Sulfate: A Convenient Hypervalent Iodine Reagent for Oxidation of Organic Sulfides and Alkenes

  作者 YUSUBOV MEHMAN S; YUSUBOVA ROSA Y; FUNK TATYANA V; CHI KIWHAN; ZHDANKIN VIKTOR V  
  选自 期刊  Synthesis;  卷期  2009年-15;  页码  2505-2508  
  关联知识点  
 

[摘要]Oligomeric iodosylbenzene Sulfate, (PhIO)(3)center dot SO3, which can be formally considered as a partially depolymerized activated iodosylbenzene, is a readily available, stable, and water-soluble hypervalent iodine reagent that is useful for the oxidation of sulfides or alkenes. Furthermore, this reagent can be conveniently generated in situ from (diacetoxyiodo)benzene and sodium bisulfate and used without isolation in oxidations in aqueous Solution or under solvent-free conditions. The reaction of iodosylbenzene sulfate in situ With organic sulfides at room temperature affords sulfoxides in high yields without over-oxidation to sulfones, and this reaction is compatible with the presence in the Substrate molecule of hydroxy groups, double bonds, benzylic carbon atoms, carboxylate groups, and various Substituted phenyl rings. The reaction of an alkene with iodosylbenzene Sulfate generated in situ results in oxidative rearrangement to form a ketone or aldehyde.

 
      被申请数(0)  
 

[全文传递流程]

一般上传文献全文的时限在1个工作日内