Abstract
2,4-Dihydroxyphenoxyacetophenones were obtained by the reaction of resorcinol with phenoxyacetonitrile under the conditions of the Houben-Hoesch reaction. Their cyclization under the conditions of acid and alkaline catalysis gave new derivatives of 3-phenoxychromone.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
References
N. V. Gorbulenko, A. V. Turov, and V. P. Khilya, Khim. Geterotsikl. Soedin., No. 4, 505 (1995).
P. J. Macander, Plant Flavonoids in Biology and Medicine, New York (1986), p. 489.
S. A. Vasil'ev, M. S. Luk'yanchikov, G. I. Molchanov, V. D. Turubarov, and V. P. Khilya, Khim. Farm. Zh.,25, No. 7, 34 (1991).
S. A. Vasil'ev, V. L. Boyarchuk, and M. S. Luk'yanchikov, Khim. Farm. Zh.,25, No. 11, 50 (1991).
V. P. Khilya, S. A. Vasil'ev, M. S. Luk'yanchikov, and V. V. Kabachnii, Visnik Kiivs'kogo Universitetu, 626 (1991).
Adams (ed.) Organic Reactions [Russian translation], Izdatinlit, Moscow (1951), p. 301.
Additional information
For Communication 18, see [1].
Chemical Faculty, Taras Shevchenko Kiev University, Kiev 252033. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 598–603, May, 1997.
Rights and permissions
About this article
Cite this article
Arkhipov, V.V., Smirnov, M.N. & Khilya, V.P. Chemistry of modified flavonoids. Chem Heterocycl Compd 33, 515–519 (1997). https://doi.org/10.1007/BF02291930
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF02291930