Alkenyl- and aryl[2-(hydroxymethyl)phenyl]dimethylsilanes: Tetraorganosilanes for the practical cross-coupling reaction

dc.contributor.author Nakao, Yoshiaki
dc.contributor.author Sahoo, Akhila K.
dc.contributor.author Imanaka, Hidekazu
dc.contributor.author Yada, Akira
dc.contributor.author Hiyama, Tamejiro
dc.date.accessioned 2022-03-27T08:35:27Z
dc.date.available 2022-03-27T08:35:27Z
dc.date.issued 2006-02-01
dc.description.abstract Readily accessible and highly stable alkenyl- and aryl[2-(hydroxymethyl) phenyl]dimethylsilanes cross-couple with various aryl and alkenyl halides under mild reaction conditions employing K2CO3 as a base at 35-80 °C. The reaction tolerates a diverse range of functional groups including silyl protections. The silicon residue, cyclic silyl ether, is readily recovered and reused on a gram-scale synthesis. Intramolecular coordination of a proximal hydroxyl group is considered to efficiently form pentacoordinated silicates having a transferable group at an axial position. © 2006 IUPAC.
dc.identifier.citation Pure and Applied Chemistry. v.78(2)
dc.identifier.issn 00334545
dc.identifier.uri 10.1351/pac200678020435
dc.identifier.uri https://www.degruyter.com/document/doi/10.1351/pac200678020435/html
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11071
dc.subject Biaryl
dc.subject Cross-coupling
dc.subject Homogeneous catalysis
dc.subject Palladium
dc.subject Silicon
dc.title Alkenyl- and aryl[2-(hydroxymethyl)phenyl]dimethylsilanes: Tetraorganosilanes for the practical cross-coupling reaction
dc.type Journal. Conference Paper
dspace.entity.type
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