The Magazine of Chemistry Europe

Reaction with allyl aryl ethers using Co(III) catalysis

Reaction involves cleavage of the N–O bond in cyanoximes promoted by SmI₂

Environmentally benign synthesis requires only a base and molecular oxygen

Brominative annulation of 2‐alkynylaryloate esters using an in-situ-generated bromoiodane

Rhodium(III)-catalyzed C–H activation and annulation in ethanol

Reaction under UV-A light gives phenols and aliphatic alcohols

Tetrabutylammonium acetate acts as base, ligand, and solvent, providing a simple and efficient synthesis route

Condensation of cyclic β-diketones, arylglyoxals, and arylhydrazones

Regio- and stereoselective reaction gives a variety of lactones with a tetrasubstituted carbon and a trichloromethyl group

A wide range of imines were hydrosilylated using a variety of silanes, catalyzed by electronically unsaturated cationic aluminum hydrides