Iridium-catalyzed Mizoroki-Heck-Type reaction of organosilicon reagents

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Abstract

Independent of substrate and solvent, the C-C bond-forming reaction of organosilicon reagents with α,β-unsaturated carbonyl compounds can be catalyzed by an iridium complex to give exclusively the Mizoroki-Heck-type addition/elimination product (see scheme). This result sharply contrasts the analogous reaction with a rhodium catalyst under similar conditions in which the 1,4-addition product is obtained preferentially. cod=cycloocta-1,5-diene.

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Koike, T., Du, X., Sanada, T., Danda, Y., & Mori, A. (2003). Iridium-catalyzed Mizoroki-Heck-Type reaction of organosilicon reagents. Angewandte Chemie - International Edition, 42(1), 89–92. https://doi.org/10.1002/anie.200390061

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