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Ruthenium-catalyzed ring-closing metathesis to form tetrasubstituted olefins
Authors:Berlin Jacob M  Campbell Katie  Ritter Tobias  Funk Timothy W  Chlenov Anatoly  Grubbs Robert H
Institution:The Arnold and Mabel Beckman Laboratories of Chemical Synthesis, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
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.
Keywords:
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