Journal of Sulfur Chemistry · 2005 · 24 citations · 13 references
Natural SciencesChemistryBioorthogonal ChemistryGreen ChemistryRedox BiochemistryCross-coupling ReactionsDisulfide Bond FormationDisulfide Bond CleavageDisulfide Bond ReductionDisulfide ChemistryMicrowave-assisted C-h FunctionalizationOxidative CouplingOxidative Coupling ReactionsOxidative Cross-couplingThiol Chemistry
A mild and efficient method for the oxidative coupling of thiols by tripropylammonium chlorochromate in solution and in solution under microwave radiation is reported. Tripropylammonium chlorochromate is an efficient and new reagent, is easily prepared, and rapidly oxidizes thiols to the corresponding disulfides. The reactions proceed cleanly and stop at the disulfide stage without over-oxidation to side-products. The simple procedure and work-up, short reaction times, and excellent yields are all advantages of this reagent.
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Reagents for Organic Synthesis
Richard C. Larock · Journal of Organometallic Chemistry · 1976 · 2.3K citations
Heterogeneous Permanganate Oxidation of Thiols
Nazih A. Noureldin, Marguerite Caldwell, Jennifer Hendry et al. · Synthesis · 1998 · 99 citations