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 |