Journal
SYNLETT
Volume 26, Issue 7, Pages 911-914Publisher
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0034-1380141
Keywords
nickel-catalyzed; disulfides; cross-coupling; 1,3,4-oxadiazole; sulfur-transfer reagents
Categories
Funding
- Ilam University Research Council
Ask authors/readers for more resources
A simple, one pot, efficient, and novel protocol has been developed for the direct synthesis of symmetrical organic disulfides using a domino reaction between an aryl/alkyl halide and potassium 5-methyl-1,3,4-oxadiazole-2-thiolate in the presence of NiCl2 as catalyst. A variety of symmetrical aryl/alkyl disulfides can be obtained in moderate to excellent yields (up to 95%).
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available