Development of novel technologies for the efficient and reversible capture of CO2 is highly
desired. In the last decade, CO2 capture using ionic liquids has attracted intensive attention …

The past decades have witnessed rapid development in organic synthesis via catalysis,
particularly the reactions through C–H bond functionalization. Transition metals such as Pd …

A new ruthenium-catalyzed, heteroatom-directed strategy for C–H allylation of indoles is
described. The use of allyl alcohols as coupling partners as well as pyridine as the …

There has been a persistent impetus for the development of versatile C− H functionalization
reactions, which represents a powerful approach to a wide variety of valuable chemical …

Alkenylpyridines are important pharmaceutical cores as well as versatile building blocks in
organic synthesis. Heck reaction represents one of the most powerful platform for the …

An efficient ruthenium-catalyzed oxidative coupling of indoles and pyrroles with various
alkenes at the C2-position assisted by employing the N, N-dimethylcarbamoyl moiety as a …

Direct allylation of aromatic and α,β-unsaturated carboxamides under ruthenium catalysis -
Chemical Communications (RSC Publishing) DOI:10.1039/C4CC03354J Royal Society of …

A highly efficient and selective Ru-catalyzed direct C2-olefination of indoles, pyrroles, and
carbazoles assisted by a removable N-dimethylcarbamoyl group has been developed by …

Abstract The catalytic C H addition of pyridines to allenes has been achieved for the first
time by using a half‐sandwich scandium catalyst, thus constituting a straightforward and …

Electron‐deficient aromatic heterocycles, such as pyridine, quinoline, and isoquinoline,
occupy a vast and rapidly expanding area of chemistry because of the obvious application of …