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Chemistry of heteroanalogs of isoflavones. 16. Benzthiazole analogs of isoflavones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The reaction of a-(2-benzthiazolyl)-2, 4-dihydroxy-5-alkylacetophenones with anhydrides and chlorides of carboxylic acids yielded 3-(2-benzthiazolyl)chromones with electron-acceptor and electron-donor substituents, as well as chromones unsubstituted in the 2 -position. Their acylation, alkylation, and aminoacylation reactions and their interaction with electrophilic and nucleophilic reagents were studied.

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Authors
  1. N. V. Gorbulenko
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  2. M. S. Frasinyuk
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  3. V. P. Khilya
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Additional information

Taras Shevchenko Kiev University, Kiev 252017. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 464–471, April, 1994. Original article submitted March 5, 1994.

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Gorbulenko, N.V., Frasinyuk, M.S. & Khilya, V.P. Chemistry of heteroanalogs of isoflavones. 16. Benzthiazole analogs of isoflavones. Chem Heterocycl Compd 30, 405–412 (1994). https://doi.org/10.1007/BF01169932

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