Nucleophilic silicon transfer to imines made possible with a copper/N-heterocyclic carbene catalyst

N-formylmorpholine is the key to producing the 1,2-cis α-glycosidic bonds of oligosaccharides

Aerobic photocatalytic oxidation, [3+2] cycloaddition, and aromatization lead to desired products

Controlling reaction kinetics allows preparation of lower-symmetry nanoparticles

Anion radical coupling yields vertically fused polycyclic aromatic heterocycles

Push-pull naphthalene diimide (NDI) motifs form the basis of redox molecular switches

Chiral thiohydantoins derived from natural α-amino acids are the key catalysts

Four enantiomers of beta-lactams produced from a single starting material

Surface-initiated ring-opening polymerization forms semiconductor films on silicon

Substituents and physical states of o-carboranes can be used to accurately control emission properties