Disulfides are widely found in natural products and find a wide range of applications in life
sciences, materials chemistry and other fields. The preparation of disulfides mainly rely on …

Organic unsymmetrical disulfides have been extensively applied in various academic and
industrial fields including intermediates in organic synthesis, agriculture, and food science …

Due to the high reactivity and versatility of benzenesulfonothioates, significant
advancements have been made in constructing CS bonds. However, there are certain …

A copper (I)‐catalyzed asymmetric, three‐component interrupted Kinugasa reaction has
been developed. Diverse chiral sulfur‐containing chiral β‐lactams with two consecutive …

In this study, we outline a general method for photocatalyzed difunctionalization of alkenes,
a diene, alkynes, 1, 3‐enynes, and [1.1. 1] propellane using dithiosulfonate reagents (ArSO2 …

Sulfur-sulfur motifs widely occur in vital function and drug design, which yearns for
polysulfide construction in an efficient manner. However, it is a great challenge to install …

Radical substitution on tetrasulfides is demonstrated to be a highly effective means to
prepare unsymmetric disulfides. Alkyl and aryl radicals generated thermally or …

The direct conversion of carboxylic acids into disulfides is described. The approach employs
oxidative photocatalysis for base‐promoted decarboxylation of the substrate, which yields …

Synthetic methods for unsymmetrical disulfides are greatly needed owing to their
applications in drug discovery, linker chemistry, and materials sciences. In this study, a new …

Sulfur‐containing alkynes, are important starting materials and intermediates in organic
reactions. Some of sulfur‐containing alkynes display interesting bioactivities and are …