Ruthenium Carbene Complexes with N,N‘-Bis(mesityl)imidazol-2-ylidene Ligands: RCM Catalysts of Extended Scope
The Journal of Organic Chemistry2000Vol. 65(7), pp. 2204–2207
Citations Over TimeTop 1% of 2000 papers
Abstract
The ruthenium carbene complexes 3a,b bearing imidazol-2-ylidene ligands constitute excellent precatalysts for ring-closing metathesis (RCM) reactions allowing the formation of tri- and tetrasubstituted cycloalkenes. They also apply to annulations that are beyond the scope of the standard Grubbs carbene 1 as well as to ring-closing reactions of acrylic acid derivatives even if the resulting alpha,beta-unsaturated lactones (or lactams) are tri- or tetrasubstituted. The reactivity of 3a was found to be highly dependent on the reaction medium: particularly high reaction rates are observed in toluene, although this solvent also leads to an increased tendency of the catalyst to isomerize the double bonds of the substrates.
Related Papers
- → Efficient transfer hydrogenation of ketones in the presence of ruthenium N-heterocyclic carbene catalysts(2006)72 cited
- → Synthesis and dynamic behaviour of a dimeric ruthenium benzylidene complex bearing a truncated N-heterocyclic carbene ligand(2017)5 cited
- → Heterogeneous, Bimetallic Metathesis Catalysts by Reaction of Fischer‐type Carbene Complexes with Reduced Phillips Catalyst(1988)13 cited
- → Metathesis Reactions in Solid‐Phase Organic Synthesis(2010)2 cited
- → Back Cover: Ruthenium Complexes of an Abnormally Bound, Anionic N‐Heterocyclic Carbene (Chem. Eur. J. 22/2014)(2014)