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

Authors

  • B. П. Хиля Taras Shevchenko State University, Kiev 252033
  • C. П. Бондарeнко Taras Shevchenko State University, Kiev 252033
  • А. В. Туров Taras Shevchenko State University, Kiev 252033

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.

How to Cite
Khilya, V. P.; Bondarenko, S. P.; Turov, A. V. Chem. Heterocycl. Compd. 1998, 34, 587. [Khim. Geterotsikl. Soedin. 1998, 34, 666.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02290943

Downloads

Published

1998-05-25

Issue

No. 5 (1998)

Section

Original Papers