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Synthesis and Activity of a New Generation of Ruthenium-Based Olefin Metathesis Catalysts Coordinated with 1,3-Dimesityl-4,5-dihydroimidazol-2-ylidene Ligands

Organic Letters · 1999 · Vol. 1(6) · pp. 953–956
Matthias SchollSheng DingChoon Woo LeeRobert H. Grubbs

Abstract

[formula: see text] A new family of 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene-substituted ruthenium-based complexes 9a-c has been prepared starting from RuCl2(=CHPh)(PCy3)2 2. These air- and water-tolerant complexes were shown to exhibit an increased ring-closing metathesis activity at elevated temperature when compared to that of the parent complex 2 and the previously developed complex 3. In many instances the activity of these complexes also rivaled or exceeded that of the alkoxy-imido molybdenum complex 1. Catalyst loadings of as low as 0.05 mol% could be used.

Synthetic Organic Chemistry MethodsFuel Cells and Related MaterialsN-Heterocyclic Carbenes in Organic and Inorganic ChemistryChemistryRutheniumCatalysisOlefin metathesisAlkoxy groupMetathesisMolybdenumSalt metathesis reactionMedicinal chemistryRing-closing metathesis

MeSH terms

AlkenesCatalysisImidazolesLigandsRuthenium

Funding

  • Korea Science and Engineering Foundation
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