This manuscript describes facile ring-opening/cross-metathesis (ROCM) reactions between unsymmetrical norbornene derivatives and electron-rich olefins in the presence of the second-generation Grubbs' catalyst to generate highly substituted furans and pyrroles.

The IPrAuNTf2/HNTf2 co-catalyzed cyclization of N-(2-perfluoroalkyl-3-alkynyl) hydroxylamines produces pyrroles in moderate to excellent yield, whereas the AgOTf-catalyzed reaction affords cyclic nitrones in high yields.

An efficient approach for the synthesis of pyrrolo[3,2-c]quinolines (the core nucleus of the natural product martinellic acid) from protected 2-alkynylanilines via the regioselective formation of pyrroles followed by Heck and intramolecular Michael addition has been described.

This review discusses total syntheses of pyrrole-containing natural products over the last ten years, highlighting recent advances in chemistry pyrroles context their innate reactivity, and preparation complex settings.

Pyrroles are important compounds present in biological systems, used for drug synthesis and material chemistry. A typical strategy the pyrrolic ring formation is centered on Paal–Knorr reaction, where 1,4-dicarbonyl react with amines giving N-substituted pyrrole derivatives. Often, main problem of this approach availability appropriate carbonyl compounds. Here, we report a sustainable carboxyli...

Calixphyrins are a class of hybrid molecules that lie at the structural crossroads between porphyrins and calixpyrroles. Porphyrins, long known for their versatile metal cation coordination chemistry, are macrocycles that contain only sp2-hybridized bridging meso carbon atoms within their framework. Calix[n]pyrroles, on the other hand, are porphyrin analogs that contain pyrroles bridged exclusi...

We report the synthesis of quinolines using cyclopropenes and an azidobenziodazolone (ABZ) hypervalent iodine reagent as azide radical source under visible-light irradiation. Multisubstituted quinoline products were obtained in 34–81% yield. The reaction was most efficient for 3-trifluoromethylcyclopropenes, affording valuable 4-trifluoromethylquinolines. transformation probably proceeds throug...

Substituted pyrroles are an essential class of heterocyclic compounds. In this research, an efficient and eco-friendly method has been developed for the synthesis of pyrrole derivatives from the reaction of 2,5-hexanedione and primary amines. Magnetic nanoparticles supported on functionalized. 7-aminonaphthalene-1,3-disulfonic acid-functionalized. silica (Fe3O4@SiO2@Propyl–ANDSA) has been inves...

Calix[4]pyrroles can be obtained from the efficient preprogrammed condensation between acetone and pyrrole. This reaction forms attractive macrocycle resembling in its constitution, but not oxidation state, to porphyrin structure, prominently present vital “pigments of life”. Calix[2]pyrrolidine[2]pyrrole calix[4]pyrrolidine, partially totally reduced version macrocycle, became accessible throu...