Ethylenebis(N-methylimidazolium) Chlorochromate (EBMICC): An Efficient and Selective Reagent for the Oxidation of Thiols to Disulfides |
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Authors: | Rahman Hosseinzadeh Mahmood Tajbakhsh Hamid Khaledi Keivan Ghodrati |
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Affiliation: | (1) Department of Chemistry, Mazandaran University, Babolsar, Iran |
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Abstract: | Summary. Ethylenebis(N-methylimidazolium) chlorochromate was prepared by addition of N-methylimidazole to 1,2-dibromoethane to form the corresponding dibromide salt and subsequent treatment of this salt with CrO3 in 6N HCl solution. It is a stable yellow-orange solid, which oxidized thiols to the corresponding disulfides at room temperature. Selective oxidation of thiols in the presence of sulfides and hydroxyl groups was also achieved with this reagent. |
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Keywords: | . Ethylenebis(N-methylimidazolium)chlorochromate Oxidation Thiols Sulfides. |
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