Abstract
Silyl ethers can be produced from alcohols and vinylsilanes under a rhodium(I) catalyst. The reaction is believed to proceed through an O-H bond cleavage of alcohol by rhodium(I) complex and a subsequent hydride insertion into vinylsilane followed by β-silyl elimination of the resulting β-silylethyl rhodium(III) complex.
Original language | English |
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Pages (from-to) | 771-775 |
Number of pages | 5 |
Journal | Synlett |
Issue number | 5 |
DOIs | |
Publication status | Published - 2006 Mar 17 |
All Science Journal Classification (ASJC) codes
- Organic Chemistry