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Title: | Rhodium-catalyzed coupling reactions with acyl- and vinylsilanes | Authors: | Yue, Yanni | Keywords: | DRNTU::Science::Chemistry | Issue Date: | 2012 | Source: | Yue, Y. (2012). Rhodium-catalyzed coupling reactions with acyl- and vinylsilanes. Doctoral thesis, Nanyang Technological University, Singapore. | Abstract: | Organosilicon compounds have attracted synthetic organic chemists because they have a potential to be used as the organometallic reagents which are stable in the air and water. As the recent transition metal-catalyzed reactions developed, catalytic reactions with organosilicon compounds have been also studied. However, most of the reported transition metal-catalyzed reactions with organosilicon compounds require the addition of at least a stoichiometric amount of fluoride salt and/or the introduction of heteroatom such as halogen or alkoxy group on the silicon atom. These activation methods are not economical because fluoride sources are expensive. Introduction of a heteroatom on the silicon atom makes the reagents unstable against hydrolysis and self-condensation. Thus synthetic organic chemists have studied on the methods to activate C–Si bonds of tetraorganosilicon compounds without adding any additional reagents. In this thesis, the author describes a novel synthetic reaction of tetraorganosilicon compounds, triorgano(vinyl)- and triorgano(acyl)silanes, catalyzed by a rhodium complex. | URI: | https://hdl.handle.net/10356/49508 | DOI: | 10.32657/10356/49508 | Schools: | School of Physical and Mathematical Sciences | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | SPMS Theses |
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File | Description | Size | Format | |
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TspmsG0703460A.pdf | main artical and experiment data | 1.61 MB | Adobe PDF | View/Open |
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