Olefins are important building blocks and are widely utilized in synthetic organic chemistry.
Owing to its omnipresence and unique reactivity, the functionalization of alkenes has …

In the area of synthetic chemistry, there are various examples of inexpensive, highly
abundant and less toxic transition-metal catalyzed inert C–H bond activation reactions …

An efficient ruthenium (II)-catalyzed tandem C–C/C–N bond formation with aryl amides and
7-azabenzonorbornadienes has been developed to synthesize cis-fused dihydrobenzo [c] …

Metal‐catalyzed asymmetric C− H bond annulation strategy offers a versatile platform,
allowing the construction of complex P‐chiral molecules through atom‐and step‐economical …

An efficient and straightforward strategy for the synthesis of isoquinolones through [4+ 2]-
annulation of N-chlorobenzamides with vinyl acetate in the presence of CoCp*(III) catalyst in …

An efficient and new route for the synthesis of (E)-4-benzylideneisochroman-1-ones through
tandem cascade annulation of benzoic acids with alkylidenecyclopropanes using Ru (II) as …

A Co (III)-catalyzed redox-neutral [4+ 2] annulation of N-chlorobenzamides/acrylamides with
substituted alkenes at ambient temperature is demonstrated. Using this protocol …

Co (III)-catalyzed regio-and chemoselective redox-neutral C–H annulation of arylamides/
acrylamides with 1, 3-dienes is described. The present annulation reaction was well suited …

The C (8)-selective nucleophilic cascade cyclization of quinoline N-oxide with easily derived
1, 6-enyne from phenol derivatives is demonstrated. A variety of quinoline N-oxide and …

An effective method for the synthesis of quinolino [2, 1-b] quinazolinones has been
described. The O-directing Rh (III)-catalyzed C–H activation of 3-arylquinazolinones and …