Abstract
Two [3+1] fragmentations of the Lewis acid stabilized bicyclo[1.1.0]tetraphosphabutanide Li[Mes*P4⋅ BPh3] (Mes*=2,4,6-tBu3C6H2) are reported. The reactions proceed by extrusion of a P1 fragment, induced by either an imidazolium salt or phenylisocyanate, with release of the transient triphosphirene Mes*P3, which was isolated as a dimer and trapped by 1,3-cyclohexadiene as a Diels–Alder adduct. DFT quantum chemical computations were used to delineate the reaction mechanisms. These unprecedented pathways grant access to both P1- and P3-containing organophosphorus compounds in two simple steps from white phosphorus.
| Original language | English |
|---|---|
| Pages (from-to) | 285-290 |
| Journal | Angewandte Chemie-International Edition |
| Volume | 56 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 2017 |
Keywords
- Anions
- fragmentation
- Lewis acids
- organophosphorus compounds
- Phosphorus