Sammanfattning
The equilibrium profiles for [1,5]-silatropic shifts in a series of 1,3-/1,1-disilyl substituted indenes were studied by NMR and computational methods based on density functional theory. Both methods indicate higher activation parameters for the [1,5]-shifts than observed in monosilyl substituted indene analogues.
| Originalspråk | Odefinierat/okänt |
|---|---|
| Sidor (från-till) | 9417–9422 |
| Antal sidor | 6 |
| Tidskrift | Tetrahedron |
| Volym | 62 |
| Nummer | 40 |
| DOI | |
| Status | Publicerad - 2006 |
| MoE-publikationstyp | A1 Tidskriftsartikel-refererad |
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