Chemistry of modified flavonoids. 19. Synthesis of phenoxyl analogs of isoflavone

Authors

  • B. B. Архипов Taras Shevchenko Kiev University, Kiev 252601
  • М. Н. Смирнов Taras Shevchenko Kiev University, Kiev 252601
  • B. П. Хиля Taras Shevchenko Kiev University, Kiev 252601

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.

How to Cite
Arkhipov, V. V.; Smirnov, M. N.; Khilya, V. P.  Chem. Heterocycl. Compd. 1997, 33, 515. [Khim. Geterotsikl. Soedin. 1997, 598.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02291930

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Published

1997-05-25

Issue

No. 5 (1997)

Section

Original Papers