Electrophilic substitution in benzo[[<i>b[</i>]thieno- and benzo[[<i>b[</i>]furo[2,3-[<i>c[</i>]pyridines. Use of the nuclear Overhauser effect for determination of substitution position

Authors

  • C. B. Толкyнов L. M. Litvinenko Institute for Physicoorganic Chemistry and Carbon Chemistry. Ukrainian Academy of Sciences, Donetsk 340114
  • M. Н. Кальницкий L. M. Litvinenko Institute for Physicoorganic Chemistry and Carbon Chemistry. Ukrainian Academy of Sciences, Donetsk 340114
  • B. И. Дуленко L. M. Litvinenko Institute for Physicoorganic Chemistry and Carbon Chemistry. Ukrainian Academy of Sciences, Donetsk 340114

Abstract

The site of electrophilic substitution in benzo[b]thieno- and benzo[b]furo[2,3-c]pyridines has been determined using the nuclear Overhauser effect and by a method based on the difference in reactivity of the isomeric products.

How to Cite
Tolkunov, S. V.; Kal'nitskii, M. N.; Dulenko, V. I. Chem. Heterocycl. Compd. 1997, 33, 1043. [Khim. Geterotsikl. Soedin. 1997, 1199.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02253218

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Published

1997-09-25

Issue

No. 9 (1997)

Section

Original Papers