Kostanecki acylation

R] (a) Hauser, C. R. Swamer, F. W. Adams, J. T. Org. React. 1954, 8, 59. [R] (b) Ellis, G. P., Chromenes, Chromanones, and Chromones from The Chemistry of Hetereocylic Compounds, Weissberger, A. and Taylor, E. C., eds John Wiley Sons, 1977, vol. 31, New York, p.495. Note The author in the former reference refers to the formation of chromones, coumarins, and flavones as the Kostanecki acylation while the latter author calls the formation of chromones and coumarins the Kostanecki-Robinson reaction. 

Also known as Kostanecki-Robinson reaction. Transformation 1 2 represents an Allan—Robinson reaction (see page 8), whereas 1 3 is a Kostanecki (acylation) reaction ... 

There is competition between products from Allan - Robinson and Kostanecki Acylation. A search of literature shows that both product types are often classified as the latter. This is exemplified with examples, all of which are searchable under Kostanecki Acylation. 

Kostanecki acylation. Formation of chro-mones or coumarines by acylation of o-hydroxyaryl ketones with aliphatic acid anhydrides followed by cyclization. 

This reaction is related to the Allan-Robins on Annulation and Kostanecki Acylation in terms of the formation of flavones. In mechanism, this reaction is related to the Fries Rearrangement. 

Koch-Haaf Carboxylations Kochi Reaction Koenigs-Knorr Synthesis Kolbe Electrolytic Synthesis Kolbe-Schmitt Reaction Komer-Contardi Reaction Kostanecki Acylation Krafft Degradation Krapcho Decarbalkoxylation... 

Gripenberg in The Chemistry ofFlavonoid Compounds, Geissman, Ed. (New York, 1962) p 410. Mechanistic studies K. Bowden, M. Chehel-Amiran, J. Chem. Soc. Perkin Trans. II 1986, 2039. Synthetic applications P. K. Jain etal, Synthesis 1982, 221 J. Zhu etal., Chem. Commun. 1988,1549 A. V. Kalinin et al, Tetrahedron Letters 39,4995 (1998) D. C. G. Pinto et al, New J. Chem. 24, 85 (2000). Cf. Allan-Robinson Reaction Kostanecki Acylation. 

---