ISSN:
1042-7163
Keywords:
Chemistry
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
Trifluoromethylthiocopper, a versatile reagent for the introduction of the trifluoromethylthio group into organic compounds, has been prepared in a crystalline form. The thiyl radicals, generated in situ from this precursor, cause the cleavage of the 3—S bond of di- and trisulfides to give unsymmetrical di- and trisulfides. Unsymmeirical n-butyl trifluoromethyl disulfide is formed by the cleaveage of the C—S bond of n-butyl sulfide.
Additional Material:
2 Tab.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/hc.520030216
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