Despite the frequent occurrence of sulfonamides in contemporary pharmaceuticals and
agrochemicals, the synthesis of these compounds is limited by the availability of preexisting …

The conversion of abundant nitrogen into various nitrogen-containing chemicals has high
academic and economic values. Traditional artificial nitrogen cycle conversion requires high …

In this study, we present a novel, efficient method for the oxidative amination of sulfenamides
using diacetoxyiodobenzene (PhI (OAc) 2) and amines under basic conditions. This …

Herein, we present the first metal-free decarboxylative C (sp3)–C (sp3) cross-coupling of
glycine derivatives with redox-active esters through highly atom and energy economical …

Sulfur–heteroatom bonds, such as S–N bonds, are valuable motifs in pharmaceuticals and
agrochemicals, but the creation of new green synthetic methods to construct these …

Sulfur-containing compounds are very common and important heteroatom skeletons and are
widely found in natural products, pharmaceuticals and bioactive compounds. Moreover, the …

An electrochemical multicomponent synthesis of sulfonamides at room temperature in single‐
pass flow is presented. In contrast to batch‐type electrolysis, an undivided flow cell setup …

The design of efficient heterogeneous redox mediators with favorable affinity to substrate
and electrolyte are much desired yet still challenging for the development of indirect …

A thiosuccinimide enabled S–N cross-coupling strategy has been established for the
intermolecular N-sulfenylation of clinically approved sulfa drugs under additive-free …

Herein, the study reports the first electrochemical nickel‐catalyzed enantioselective hydro‐
arylation/alkenylation of enones in an undivided cell with low‐cost electrodes in the absence …