Further Information
Literature
Related Reactions
Claisen Condensation
Baker-Venkataraman Rearrangement
The base-induced transfer of the ester acyl group in an o-acylated phenol ester, which leads to a 1,3-diketone. This reaction is related to the Claisen Condensation, and proceeds through the formation of an enolate, followed by intramolecular acyl transfer.
Mechanism of the Baker-Venkataraman Rearrangement
Recent Literature
Directed ortho metalation - cross coupling links. Carbamoyl
rendition of the baker-venkataraman rearrangement. Regiospecific route to substituted 4-hydroxycoumarins
A. V. Kalinin, A. J. M. Da Silva, C. C. Lopes, R. S. C. Lopes, V. Snieckus, Tetrahedron. Lett., 1998, 39, 4995-4998.
A Convenient Method for Synthesizing 2-Aryl-3-hydroxy-4-oxo-4H-1-benzopyrans
or Flavonols
A. Fougerousse, E. Gonzalez, R. Brouillard, J. Org. Chem., 2000,
65, 583-586.