Synthèse électrochimique du cycle époxydique. Communication préliminaire

作者: Raymond Gerdil

DOI: 10.1002/HLCA.19700530820

关键词: EpoxyReductive cleavageIntramolecular forceInorganic chemistryElectrolysisCathodeElectrodeOrganic chemistryChemistryMercury (element)Polarography

摘要: The polarographic behaviour of ditosyloxy alkanes TsO(CH2)nOTs in aprotic medium suggests that intramolecular cyclisation takes place after reductive cleavage a single SO2O bond at the dropping electrode. This hypothesis was verified by controlled potential electrolysis lower homologues mercury cathode. High yields epoxy compounds are obtained this method.

参考文章(1)
Parviz Yousefzadeh, Charles K. Mann, Electrochemical reduction of alkyl esters of p-toluenesulfonic acid Journal of Organic Chemistry. ,vol. 33, pp. 2716- 2720 ,(1968) , 10.1021/JO01271A022