Palladium/norbornene cooperative catalysis has emerged as a distinct approach to
construct polyfunctionalized arenes from readily available starting materials. This Review …

The Catellani reaction is a palladium-catalyzed hydrocarbon-activated multicomponent
tandem reaction involving an aryl halide, an electrophilic coupling reagent and a terminating …

We report diverse C–N cross-coupling reactions of aryl thianthrenium salts that are formed
site-selectively by direct C–H functionalization. The scope of N-nucleophiles ranges from …

An asymmetric hydroarylative cyclization of enynes involving a C–H bond cleavage is
reported. The cobalt-catalyzed cascade generates three new bonds in an atom-economical …

C‐aryl glycosides are popular basic skeletons in biochemistry and pharmaceutical
chemistry. Herein, ruthenium‐catalyzed highly stereo‐and site‐selective ortho‐and meta …

Palladium/norbornene (Pd/NBE) cooperative catalysis has emerged as a useful tool for
preparing poly substituted arenes; however, its substrate scope has been largely restricted …

Conventional approaches on using hydroxylamine derivatives as single nitrogen sources,
for the construction of n-membered (n> 3) N-heterocycles, rely upon two chemical …

The Catellani reaction, originally discovered by Catellani in 1997, and further developed by
Catellani, Lautens and others, has emerged as a powerful strategy for the synthesis of …

Highly functionalized 4-aminoindoles were synthesized via the three-component cross-
coupling of o-iodoaniline, N-benzoyloxyamines, and norbornadiene. The Catellani and retro …

The switchable synthesis of 3-non, 3-mono, 3, 3′-disubstituted 3, 4-dihydroquinolin-2 (1 H)-
ones was developed through a redox-neutral hydride-transfer/N-dealkylation/N-acylation …