Abstract
A new type of catalytic hydrosilylation of arylalkynes was induced by a 16-electron ruthenium bis(silyl) phosphine complex, resulting in ortho-silylation of the aryl group as well as a hydrogenation of the alkyne CC bond to give an (E)-form of alkene selectively. On the other hand, the same reaction using a related bis(silyl) complex having an η6-toluene ligand instead of the phosphine ligand as a catalyst led to a normal hydrosilylation reaction to afford silylalkene. © 2008 IUPAC.
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Tobita, H., Yamahira, N., Ohta, K., Komuro, T., & Okazaki, M. (2008). New hydrosilylation reaction of arylacetylene accompanied by C-H bond activation catalyzed by a xantsil ruthenium complex. In Pure and Applied Chemistry (Vol. 80, pp. 1155–1160). https://doi.org/10.1351/pac200880051155
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