The trifluoromethyl group is found in many synthetic bioactive compounds, and the
difunctionalization of a C C bond, as a powerful strategy for the construction of compounds …

The development and application of efficient, convenient, selective, and environmentally
benign synthetic methods is highly desirable in organic chemistry. With this requirement …

Aryl nitriles are widely found in natural products, pharmaceuticals, agrochemicals, dyes, and
herbicides. Moreover, because the cyano group can be easily converted into various …

C–S bond activation, cleavage and transformations by means of transition metal compounds
have recently become more and more important in the petroleum industry and synthetic …

Abstract Die Trifluormethylgruppe ist Bestandteil vieler synthetischer bioaktiver
Verbindungen, und die Difunktionalisierung von C C‐Bindung wurde als wirksame …

Sulfinic acids and their salts have recently emerged as versatile coupling partners to
efficiently access a wide variety of hetero-and carbocyclic compounds, under relatively mild …

A simple and general method for anti-selective hydrosulfonylation of unactivated alkynes
with sulfonyl chlorides in the presence of a catalytic amount of phenanthroline-based Lewis …

Transition‐metal‐catalyzed carbon–carbon bond‐forming reactions are among the most
powerful methods in organic synthesis and play a crucial role in modern materials science …

A new, efficient protocol for the synthesis of di (hetero) aryl sulfides is described. Cheap and
easily available arylsulfonyl chlorides as a sulfur source reductively couple with electron-rich …

In recent years, palladium-catalyzed direct arylation of (hetero) aromatics with aryl halides
via a C–H bond activation has become a popular method for generating carbon–carbon …