Nucleophilic Activation Of Hydrosilanes Via A Strain-Imposing Strategy Leading To Functional Sila-Aromatics
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY(2021)
Abstract
Carefully designed cyclic hydrosilanes enable trans-selective hydrosilylation of unactivated alkynes without transition metal catalysts via silicate formation. Employment of sterically demanding bidentate ligands of silicon increases steric congestion upon silicate formation, and this strain-imposing strategy facilitates hydride transfer. This hydrosilylation provides efficient access to diverse benzosiloles, silaphenalenes, and related silacycles.
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Key words
hydrosilanes,strain-imposing,sila-aromatics
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