The bmpi (1,3-bis(6′-methyl-2′-pyridylimino)isoindoline) pincer Ru(II) hydride complex catalyzes base-free, acceptorless, and chemoselective dehydrogenation of alcohols with liberation of dihydrogen under moderate (<120 °C) conditions. Primary alcohols and diols are converted to ester and lactone products with high conversion efficiencies. The catalyst system is remarkably selective for the oxidation of secondary alcohols in the presence of primary alcohols
AbstractA convenient and selective oxidation of alcohols with aqueous hydrogen peroxide to give the ...
The catalytic properties of a series of ruthenium complexes for H/D exchange between D<sub>2</sub>O ...
Ruthenium(II) hydride complexes bearing a pyrazolyl-(2-indol-1-yl)-pyridine ligand were synthesized ...
The bmpi (1,3-bis(6′-methyl-2′-pyridylimino)isoindoline) pincer Ru(II) hydride complex catalyzes ...
An efficient, operatively simple, acceptorless, and base-free dehydrogenation of secondary alcohols ...
The diruthenium(II,II) complex [Ru2(L1)(OAc3]Cl (1), spanned by a naphthyridine-diimine ligand and b...
International audienceSeveral dipyridylamine-Ir(III)and dipyridylamine-Ru(II)complexes have been eva...
International audienceThe ruthenium complex [RuCl2(p-cymene)(IMes)] catalyses the dehydrogenation of...
The reversible transformations between ketones and alcohols via sequential hydrogenation–dehydrogena...
A commercially available ruthenium (II) PNP type pincer catalyst (Ru-Macho) promotes formation of am...
The ruthenium complex (8-(2-diphenylphosphinoethyl)aminotrihydroquinolinyl)(carbonyl)(hydrido)ru...
The ruthenium(II) complex, [fac‐PNHN]RuH(η1‐BH4)(CO) (B; PNHN=8‐(2‐diphenylphosphinoethyl)aminotrihy...
An efficient oxidant-free oxidation for a wide range of alcohols was achieved by a recyclable ruthen...
This paper presents an outstanding air-stable ruthenium catalyst that has unprecedented efficiency (...
A new method for the direct synthesis of imines from alcohols and amines is described where hydrogen...
AbstractA convenient and selective oxidation of alcohols with aqueous hydrogen peroxide to give the ...
The catalytic properties of a series of ruthenium complexes for H/D exchange between D<sub>2</sub>O ...
Ruthenium(II) hydride complexes bearing a pyrazolyl-(2-indol-1-yl)-pyridine ligand were synthesized ...
The bmpi (1,3-bis(6′-methyl-2′-pyridylimino)isoindoline) pincer Ru(II) hydride complex catalyzes ...
An efficient, operatively simple, acceptorless, and base-free dehydrogenation of secondary alcohols ...
The diruthenium(II,II) complex [Ru2(L1)(OAc3]Cl (1), spanned by a naphthyridine-diimine ligand and b...
International audienceSeveral dipyridylamine-Ir(III)and dipyridylamine-Ru(II)complexes have been eva...
International audienceThe ruthenium complex [RuCl2(p-cymene)(IMes)] catalyses the dehydrogenation of...
The reversible transformations between ketones and alcohols via sequential hydrogenation–dehydrogena...
A commercially available ruthenium (II) PNP type pincer catalyst (Ru-Macho) promotes formation of am...
The ruthenium complex (8-(2-diphenylphosphinoethyl)aminotrihydroquinolinyl)(carbonyl)(hydrido)ru...
The ruthenium(II) complex, [fac‐PNHN]RuH(η1‐BH4)(CO) (B; PNHN=8‐(2‐diphenylphosphinoethyl)aminotrihy...
An efficient oxidant-free oxidation for a wide range of alcohols was achieved by a recyclable ruthen...
This paper presents an outstanding air-stable ruthenium catalyst that has unprecedented efficiency (...
A new method for the direct synthesis of imines from alcohols and amines is described where hydrogen...
AbstractA convenient and selective oxidation of alcohols with aqueous hydrogen peroxide to give the ...
The catalytic properties of a series of ruthenium complexes for H/D exchange between D<sub>2</sub>O ...
Ruthenium(II) hydride complexes bearing a pyrazolyl-(2-indol-1-yl)-pyridine ligand were synthesized ...