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Palladium(0)-Catalyzed Silylation of Aryl Halides with Triorganosilanes: Synthesis of Aryl(2-furyl)silanes Murata, Miki Ohara, Hiroya Oiwa, Ryo Watanabe, Shinji Masuda, Yuzuru Triorganosilanes, which possess two aryl groups on the silicon atom, undergo the palladium-catalyzed silylation of aryl iodides. Aryl(2-furyl)silanes thus obtained are potentially useful starting materials for carbon-carbon bond-formation reactions in the presence of transition metal catalysts and tetrabutylammonium fluoride. application/pdf journal article Georg Thieme Verlag 2006-06 application/pdf Synthesis 11 2006 1771 1774 https://kitami-it.repo.nii.ac.jp/record/7170/files/5076.pdf https://kitami-it.repo.nii.ac.jp/records/7170 eng http://doi.org/10.1055/s-2006-942368 http://www.thieme-connect.de/ejournals/abstract/synthesis/doi/10.1055/s-2006-942368 Georg Thieme Verlag, Miki Murata, Hiroya Ohara, Ryo Oiwa, Shinji Watanabe, Yuzuru Masuda, Synthesis, 2006(11), 2006, 1771-1774. Georg Thieme Verlag, M.Murata, S.Yoshida, S-iNirei, S.Watanabe, Y.Masuda, Synlett, 2006(1), 2006, 118-120. c2006 Georg Thieme Verlag KG. open access