The first asymmetric Kumada reactions of alkyl electrophiles are described, specifically, cross-couplings of racemic alpha-bromoketones with aryl Grignard reagents. Several features of this investigation are of interest. First, the couplings proceed at remarkably low temperature (-40 or -60 degrees C), which enables the asymmetric synthesis of racemization-prone alpha-arylketones. Second, dialk...

Non-activated alkyl halides are challenging substrates for cross-coupling reactions because they are reluctant to undergo oxidative addition and because metal alkyl intermediates are prone to beta-H elimination. Despite recent progress, well-defined catalysts are rare. We recently prepared Ni complexes with a chelating pincer-type bis(amino)amide ligand. The chloride complex [((Me)NN2)NiCl] is ...

Structurally distinctive dinuclear Ni(II) complexes with furan or thiophene tethered amine-pyrazolyl tripodal hybrid ligands have been synthesized and crystallographically characterized. All complexes are catalytically active towards cross-coupling of aryl/alkyl Grignard reagents with β-H containing alkyl halides at room temperature in the presence of N,N,N',N'-tetramethylethylenediamine (TMEDA...

C functionalization of graphene significantly broadens its application potential via tuning its electronic and surface properties. Therefore, a wide range of dry and wet chemistry approaches have been developed for graphene functionalization. Despite recent progress in this field, covalent modification of graphene is still hampered by its low reactivity. Moreover, the reactivity depends on the ...

A new one-pot approach for the synthesis of aryl a-keto ester based on the diazo transfer and oxidation of diazo group is developed. 2005 Elsevier Ltd. All rights reserved. 1 3 Ar OMe O [O] Ar OMe O O Ar OMe N2 [O] Base ArSO2N3 a-Keto acids and esters have been important compounds as natural products and as the building blocks in organic synthesis. Over the past decades, various methods have be...