@article{oai:kitami-it.repo.nii.ac.jp:00007236, author = {Murata, Miki and Yamasaki, Hiyoruki and Ueta, Tsukasa and Nagata, Masayuki and Ishikura, Masanori and Watanabe, Shinji and Masuda, Yuzuru}, issue = {19}, journal = {Tetrahedron}, month = {May}, note = {The general and efficient silylation of aryl halides has developed utilizing triethoxysilane and a rhodium catalyst. The substrate scope is broad and includes ortho-, meta-, and para-substituted electron-rich and -deficient aryl iodides. In addition, the silylation of aryl bromides and fluoroalkanesulfonates proceeded in the presence of tetra-n-butylammonium iodide., NOTICE: This is the author's version of a work accepted for publication by Elsevier. Changes resulting from the publishing process, including peer review, editing, corrections, structual formatting and other quality control mechanisms , may not be reflected in this document. Changes may have been to this work since it was submitted for publication., application/pdf}, pages = {4087--4094}, title = {Synthesis of aryltriethoxysilanes via rhodium(I)-catalyzed cross-coupling of aryl electrophiles with triethoxysilane}, volume = {63}, year = {2007} }