Journal2004
EFFICIENT AND SELECTIVE OXIDATION OF THIOLS TO DISULFIDES BY 1,4-DIAZABICYCLO[2.2.2]OCTANE-DI-N-OXIDE-DI-PERHYDRATE UNDER NEUTRAL AND HETEROGENEOUS CONDITIONS
Phosphorus, sulfur, and silicon and the related elements Vol. 179, No. 9, 1777–1781
چکیده
1,4-Diazabicyclo[2.2.2]octane-di-N-oxide-di-perhydrate[3pc] selectively oxidizes thiols to disulfides in acetonitrile in good yields. The method is generally useful for a wide variety of thiols.
موضوعات و کلیدواژهها
Chemical Synthesis and ReactionsSulfur-Based Synthesis TechniquesOrganic Chemistry Cycloaddition ReactionsOctaneAcetonitrileChemistryOxideOrganic chemistryCombinatorial chemistryPhotochemistry
ارجاع علمی
Peyman Salehi, Mohammad Ali Zolfigol, Leila Bazaz Tolami. “EFFICIENT AND SELECTIVE OXIDATION OF THIOLS TO DISULFIDES BY 1,4-DIAZABICYCLO[2.2.2]OCTANE-DI-N-OXIDE-DI-PERHYDRATE UNDER NEUTRAL AND HETEROGENEOUS CONDITIONS.” Phosphorus, sulfur, and silicon and the related elements, 2004. https://doi.org/10.1080/10426500490466427