(N-Heterocyclic Carbene)2-Pd(0)-Catalyzed Silaboration of Internal and Terminal Alkynes: Scope and Mechanistic Studies

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Abstract

Pd(ITMe)2(PhC≡CPh) acts as a highly reactive precatalyst in the silaboration of terminal and internal alkynes to yield a number of known and novel 1-silyl-2-boryl alkenes. Unprecedented mild reaction temperatures for terminal alkynes, short reaction times, and low catalytic loadings are reported. During mechanistic studies, cis-Pd(ITMe)2(SiMe2Ph)(Bpin) was directly synthesized by oxidative addition of PhMe2SiBpin to Pd(ITMe)2(PhC≡CPh). This represents a very rare example of a (silyl)(boryl)palladium complex. A plausible catalyst decomposition route was also examined.

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Ansell, M. B., Spencer, J., & Navarro, O. (2016). (N-Heterocyclic Carbene)2-Pd(0)-Catalyzed Silaboration of Internal and Terminal Alkynes: Scope and Mechanistic Studies. ACS Catalysis, 6(4), 2192–2196. https://doi.org/10.1021/acscatal.6b00127

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