An Olefin Metathesis/Double Bond Isomerization Sequence Catalyzed by an In Situ Generated Ruthenium Hydride Species

Bernd Schmidt*

*Universität Potsdam, Institut für Chemie, Organische Chemie II, Karl-Liebknecht-Strasse 24-25, Haus 25, 14476 Golm, Germany, Email: berschmirz.uni-potsdam.de

B. Schmidt, Eur. J. Org. Chem., 2003, 816-819.

DOI: 10.1002/ejoc.200390124

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Abstract

An olefin metathesis/double bond migration sequence of allyl ethers to cyclic enol ethers is catalyzed by first and second generation Grubbs' catalysts. These ruthenium carbene complexes were activated to catalyze the double bond migration by additioin of hydride sources, such as NaH or NaBH₄.

see article for more examples

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Note

Our full paper provides more extensive information and details: B. J. Schmidt, J. Org. Chem. 2004, 69, 7672-7687. DOI: 10.1021/jo048937w

Bend Schmidt, August 10, 2015

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Imino Glycals via Ruthenium-Catalyzed RCM and Isomerization

B. Schmidt, S. Hauke, N. Mühlenberg, Synthesis, 2014, 46, 1648-1658.

Tandem olefin metathesis/hydrogenation at ambient temperature: activation of ruthenium carbene complexes by addition of hydrides

B. Schmidt, M. Pohler, Org. Biomol. Chem., 2003, 1, 2512-2517.

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Key Words

Homogeneous catalysis, Isomerization, Ring Closing Metathesis, Oxacycles, 2,3-Dihydrofurans, 3,4-Dihydro-2H-pyrans, Rearrangement

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ID: J24-Y2003-140