Aromatic dianionic oxy-Cope rearrangement of 1,2-dinaphthyl-1,2-diols of acyclic diketones
2008
We report the first instance where 1,2-dinaphthyl-1,2-diols of benzil and biacetyl undergo aromatic dianionic oxy-Cope rearrangement where the x bonds of the two naphthyl rings form the 1,5-hexadiene system necessary for oxy-Cope rearrangement.
- Correction
- Source
- Cite
- Save
- Machine Reading By IdeaReader
1
References
0
Citations
NaN
KQI