The last decade has witnessed a high demand of various synthetic approaches towards
bioactive achiral diarylmethanols, diaryl and triarylmethanes and the molecules derived …

Although metal-catalyzed direct arylation reactions of non-or weakly acidic C–H bonds have
recently received much attention, chemists have relied heavily on substrates with …

The selective γ-C (sp3)–H carbonylation of N-(2-pyridyl) sulfonyl (N-SO2Py)-protected
amines has been accomplished by using palladium catalysis and Mo (CO) 6 as carbonyl …

Abstract The first Cp* RhIII‐catalyzed arylation of unactivated C (sp3) H bonds is
presented. The unactivated primary C (sp3) H bond of 2‐alkylpyridines can be activated by …

An unprecedented protocol has been developed for the regioselective synthesis of
structurally diverse indene derivatives from readily accessible N-benzylic sulfonamides and …

Nickel (0)-catalyzed cross-coupling of heteroaryl-containing diarylmethanes with both aryl
bromides and chlorides has been achieved. The success of this reaction relies on the …

Chemical bond cleavage and reconstruction are common processes in traditional
rearrangement reactions. In contrast, the process that involves bond cleavage, fragment …

An unprecedented catalyst-free alkylation of sulfinic acids with sulfonamides has been
developed via sp3 C− N bond cleavage at room temperature. In the absence of external …

An efficient, general, and one-pot procedure for the synthesis of multisubstituted xanthene
derivatives through Fe (III)-catalyzed reactions of 2-aryloxybenzaldehydes with electron-rich …

A method to prepare α-acyl-β-amino acid and 2, 2-diacyl aziridine derivatives efficiently from
Cu (OTf) 2+ 1, 10-phenanthroline (1, 10-phen)-catalyzed amination and aziridination of 2 …