Organic compounds possessing S–S bonds, often called disulfides or more specifically
disulfanes, have been widely applied in various fields ranging from biochemistry to different …

Disulfide, as a common structural motif, has been frequently used in pharmaceuticals, nature
products, and chemical biology. This chapter focuses on the methodologies that were …

This review summarizes the recent developments of disulfide bond formation with a variety
of reagents. The scope and limitations of the presented methods are discussed. The …

Alkyl, aryl and heteroaryl symmetrical disulfides can be easily obtained by heating the
corresponding thiols for several hours at 80° C with Et3N in DMF under atmospheric oxygen …

Selective oxidation of sulfides to sulfoxides and sulfones is achieved by H2O2 using
MoO2Cl2 as the catalyst. Various substituted sulfides having functional groups such as …

A facile and eco‐friendly visible light‐mediated synthesis of symmetrical and unsymmetrical
disulfides using tris [2‐phenylpyridinato‐C2, N] iridium (III) under additive and oxidant free …

The bio-based green solvent ethyl lactate has been found to be a particularly efficient
medium for oxidative coupling reactions of thiols yielding a broad array of disulfides. As a …

A serendipitiously discovered, extremely simple, fast and previously unreported method for
the preparation of symmetrical aliphatic, aromatic and heteroaromatic disulfides is reported …

A novel sustainable strategy for the synthesis of phenols has been developed using
inexpensive, readily available, air-stable, and recyclable CuFe 2 O 4 nanoparticles as the …

Chromium (VI) is established as a versatile oxidant for many types of substrates varying from
metal ions to naturally occurring organic compounds, and has a wide range of applications …