Lawesson's reagent (LR) is a well-known classic example of a compound with unique
construction and unusual chemical behavior, with a wide range of applications in synthetic …

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 …

Transition‐metal‐catalyzed C− H bond functionalization has emerged as a powerful tool in
contemporary organic synthesis. In this aspect, precious metal‐based high‐valent catalysts …

A general palladium-catalyzed aryl (alkyl) thiolation of various substituted unactivated
arenes is accomplished for the synthesis of diverse unsymmetrical diaryl (alkyl) sulfides in …

A novel method for the preparation of alkyl aryl sulfides through direct oxidation thiolation of
commercial ethers with diaryl disulfides using di-tert-butyl peroxide (DTBP) as the oxidant …

An efficient Cu-catalyzed one-pot approach for the synthesis of unsymmetrical diaryl
thioethers using potassium ethyl xanthogenate as a thiol surrogate is developed. This new …

Pd2(dba)3/Xantphos-catalyzed cross-coupling of thiols and aryl bromides/triflates -
ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & Books Search …

A novel and highly regioselective ammonium iodide-induced nonradical sulfenylation
method for the construction of a C–S bond was developed via C–H functionalization. With …

Diaryl thioethers and S-cycles were obtained on the basis of the copper-catalyzed reaction
of carbon disulfide and aryl iodides in the presence of DBU. This reaction enables the one …

Transition-metal-free synthetic methods have been developed for the preparation of
unsymmetrical diaryl and aryl alkyl chalcogenides: sulfones, sulfides, and selenides from the …