Issue 9, 1985

The chemistry and catalytic properties of ruthenium and osmium complexes. Part 1. Homogeneous catalysis of organic reactions by bromo(carbonyl)hydridotris(triphenylphosphine)osmium(II)

Abstract

The title compound catalyses C[double bond, length half m-dash]C bond migration, isomerisation of allyl alcohol, hydrogenation of ayclic and cyclic olefins, dienes, acetylenes, aldehydes, ketones, α,β-unsaturated aldehydes and ketones, and hydroformylation of alkenes under moderate reaction conditions. High selectivities have been observed in the hydrogenation of conjugated and unconjugated dienes to monoenes, C[triple bond, length half m-dash]C to C[double bond, length half m-dash]C bonds, α,β-unsaturated aldehydes to unsaturated alcohols, and α,β-unsaturated ketones to saturated ketones; L-carvone [2-methyl-5-(1-methylethenyl)cyclohex-2-en-1-one] may be selectively reduced to 2-methyl-5-(1-methylethyl)cyclohex-2-en-1-one or 2-methyl-5-(1-methylethyl)cyclohexanone depending on the reaction conditions.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1985, 1859-1863

The chemistry and catalytic properties of ruthenium and osmium complexes. Part 1. Homogeneous catalysis of organic reactions by bromo(carbonyl)hydridotris(triphenylphosphine)osmium(II)

R. A. Sánchez-Delgado, A. Andriollo, E. González, N. Valencia, V. León and J. Espidel, J. Chem. Soc., Dalton Trans., 1985, 1859 DOI: 10.1039/DT9850001859

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