Doyle, MichaelDevora, Gene2021-11-162021-11-161994-07-01https://doi-org.libweb.lib.utsa.edu/10.1515/MGMC.1994.17.6.3952191-0219https://hdl.handle.net/20.500.12588/726Dirhodium(ll) tetraacetate in combination with catecholborane catalyzes the isomerization of alkenes and dienes. Effective isomerization occurs at 80-135°C with the use of only 0.1 mol % rhodium acetate. With 2-methyl-1,5-hexadiene the disubstituted double bond is preferentially isomerized. In addition, hydrogen transfer hydrogenation occurs with 1,4-cyclohexadienes. The mechanism of these reactions is proposed to involve organoborane addition across a Rh-0 bond which activates the catalyst for isomerization and hydrogenation.en-USAttribution 3.0 United Stateshttp://creativecommons.org/licenses/by/3.0/us/Highly Efficient Olefin Isomerization Catalyzed by Metal Hydrides Derived from Dirhodium(II) Carboxylates and CatecholboraneArticle