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For this reason, the development of transition metal oxide catalysts as alternatives has gained much interest.
In order to circumvent these complications, a meticulous effort has been focused on the development of transition metal-catalyzed coupling of thiophenols with aryl halides.
However, only until recently has considerable progress been made thanks to the enormous development of transition metal olefin polymerization catalysis (Ziegler-Natta, metallocene and post-metallocene).
The development of transition metal based heterogeneous catalysts with efficient reactivity and intensive stability is of great demand in peroxymonosulfate based AOPs in water treatment.
Our findings may help the development of transition metal poly-phosphide with precise phase controlling technique for applications in hydrogen production.
The traditional types of water-soluble catalysts applied in aqueous media are outlined together with recent trends towards the development of transition metal nanoparticle and nanocomposite catalysts.
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His lab is engaged in three main topics: the study of secondary metabolites containing unusual pharmacophores, the design of combinatorial routes to neurotransmitter receptor ligands, and the development of transition-metal-catalyzed hydrogen-atom-transfer reactions.
The Sawamura laboratory has pioneered the development of transition-metal-catalyzed stereospecific allylic substitution reactions using arylboron nucleophiles.
This understanding in turn can instruct the development of transition-state analogue inhibitors, which have exciting potential as drug candidates.
In recent years, notable progress has been made in the development of transition-metal-based catalysts for the formation of C N bonds, in particular through mechanisms involving metal nitrenoid C H insertion reactions.
As in the development of transition-metal-catalyzed asymmetric cross-coupling reactions, the first explorations of asymmetric allylic substitution involved the Ni-catalyzed reaction of organomagnesium reagents in the presence of chiral phosphines.
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