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Synthesis of pyridine and quinoline analogs of chalcone. Study of their structure by the PMR method

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Substituted pyridine and 2-quinoline analogs of chalcone have been synthesized. The homonuclear Overhauser effect has been used to assign the PMR signals of the olefinic protons of the indicated pyridine derivatives and to elucidate their steric orientation.

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Authors
  1. V. P. Khilya
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  2. S. P. Bondarenko
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  3. A. V. Turov
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Additional information

Taras Shevchenko State University, Kiev 252033, Ukraine. Translated from Khimiya Geterotsiklicheskikh soedinenii, No. 5, pp. 666–670, May, 1998.

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Khilya, V.P., Bondarenko, S.P. & Turov, A.V. Synthesis of pyridine and quinoline analogs of chalcone. Study of their structure by the PMR method. Chem Heterocycl Compd 34, 587–591 (1998). https://doi.org/10.1007/BF02290943

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  • DOI: https://doi.org/10.1007/BF02290943

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