Ruthenium-Catalyzed Ring-Closing Metathesis to Form Tetrasubstituted Olefins
Organic Letters2007Vol. 9(7), pp. 1339–1342
Citations Over TimeTop 1% of 2007 papers
Abstract
[structure: see text]. Increased efficiency for ring-closing metathesis to form tetrasubstituted olefins using N-heterocyclic carbene ligated ruthenium catalysts was achieved by reducing the size of the substituents at the ortho positions of the N-bound aryl rings.
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