Abstract
A range of bis(trimethylsilyl)methyl-substituted aryl derivatives was prepared by using a Kumada-Corriu cross-coupling reaction. The regioselective metalation of the resulting bis(trimethylsilyl)methyl-substituted aryl derivatives bearing this bulky silyl group allowed the generation of functionalized aromatics. A regioselective switch in the presence or in the absence of the bis(trimethylsilyl)methyl group has been demonstrated. Furthermore, this silyl group was converted into a formyl group or a styryl group, enhancing the scope of application of such bis(trimethylsilyl)methyl- substituted arenes.
| Original language | English |
|---|---|
| Pages (from-to) | 8338-8342 |
| Number of pages | 5 |
| Journal | Chemistry - A European Journal |
| Volume | 20 |
| Issue number | 27 |
| DOIs | |
| State | Published - 1 Jul 2014 |
Keywords
- aromatics
- lithiation
- magnesium
- metalation
- silyl reagents
All Science Journal Classification (ASJC) codes
- Catalysis
- Organic Chemistry