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• W2090370607 endingPage "1103" @default.
• W2090370607 startingPage "1103" @default.
• W2090370607 abstract "A convenient and efficient procedure has been developed for the vinylation of aryl-, styrenyl-, cinnamyl- and dienyl-halides by a Pd(0) nanoparticle-catalyzed Hiyama cross-coupling to provide the corresponding dienes and trienes in high yields. The reaction does not require any ligand or co-catalyst, and is carried out using PdCl2 and tetrabutyl ammonium fluoride (TBAF) in THF. Pd nanoparticles are generated in situ and are the active catalytic species in this reaction. A wide range of functionalized styrenes, trans aryl 1,3-, 1,4- and 1,5- dienes, 1,2-, 1-3 and 1,4-bis(1,3-dienes), and 1,3,5-trienes can be obtained by this procedure." @default.
• W2090370607 created "2016-06-24" @default.
• W2090370607 creator A5019027975 @default.
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• W2090370607 date "2011-01-01" @default.
• W2090370607 modified "2023-09-25" @default.
• W2090370607 title "An easy access to styrenes: trans aryl 1,3-, 1,4- and 1,5-dienes, and 1,3,5-trienes by Hiyama cross-coupling catalyzed by palladium nanoparticles" @default.
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• W2090370607 doi "https://doi.org/10.1039/c0nj01019g" @default.
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