A General Palladium-Catalyzed Coupling of Aryl Bromides/Triflates and Thiols

Takahiro Itoh, Toshiaki Mase

Organic Letters · 2004 · 472 citations · 17 references

Concepts

Abstract

We have developed an efficient palladium-catalyzed carbon-sulfur bond formation reaction of aryl bromides, triflates, and activated aryl chloride. Using this protocol, we have shown tolerance to a wide variety of aryl thiols and alkyl thiols that can also be used as sulfide equivalents. [reaction: see text]

References

17