The challenges of the modern society and the growing demand of high-technology sectors
of industrial production bring about a new phase in the development of organic synthesis. A …

The development of practical and efficient methods for C–C and C–X bond formation has
attracted a great deal of current attention with the advent of C–H functionalization reactions …

A convenient and efficient transition-metal-free protocol for the synthesis of 3-alkyl
quinoxalin-2 (1H)-ones from the radical reaction of quinoxalin-2 (1H)-ones with ethers was …

Copper-catalyzed oxidative carbon–heteroatom bond formation: a recent update - Chemical
Society Reviews (RSC Publishing) DOI:10.1039/C5CS00882D Royal Society of Chemistry …

The present review summarizes primary publications on the cross-dehydrogenative C–O
coupling, with special emphasis on the studies published after 2000. The starting …

The cleavage of an unactivated aryl nitro group triggered by alkyl radicals enables a
dearomative cyclization, affording diversified alkylated spiro [5.5] trienones in good yields …

A copper-catalyzed cross-dehydrogenative coupling strategy has been developed for the
synthesis of two classes of esters from simple solvents. The reaction of methylarenes with …

An efficient metal free protocol has been developed for the synthesis of benzylic esters via a
cross dehydrogenative coupling (CDC) involving alkylbenzene (s) as a self-or as a cross …

Trichloroisocyanuric acid (TCCA) is a versatile and efficient reagent for chlorination and
oxidation reactions. Depending on the reaction conditions employed, it can release either an …

The first selective coupling of a carbon nucleophile with methyl, ethyl, propyl, and butyl
arenes in the absence of a directing group is described. Pd (OAc) 2 double C–H activation …