ACYLATION OF 3-ACYL-2-METHYLBENZO[<i>b</i>]THIOPHENE

Authors

  • В. Н. Яровенко N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
  • Л. В. Христофорова N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
  • Л. И. Беленький N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
  • А. С. Шашков N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
  • Т. К. Барышникова N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
  • М. М. Краюшкин N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

DOI:

https://doi.org/10.1007/2129

Keywords:

3-acyl-2-methylbenzo[b]thiophene, diketeones, 2-methylbenzo[b]thiophene, X-ray diffraction structural analysis, electrophilic substitution

Abstract

The effect of the nature of the catalysts, reagents, and solvents on the acylation of 3-acyl-2-methyl-benzo[b]thiophene was studied. The structure of the products was supported by the two-dimensional 1H and 13C NMR spectra (2D, HMBC).

How to Cite
Yarovenko, V. N.; Khristoforova, L. V.; Belen’kii, L. I.; Shashkov, A. S.; Baryshnikova, T. K.; Krayushkin, M. M. Chem. Heterocycl. Compd. 2011, 47(2), 166. [Khim. Geterotsikl. Soedin. 2011, 211.]

For this article in the English edition see DOI 10.1007/s10593-011-0737-9

Downloads

Published

2014-12-03

Issue

No. 2 (2011)

Section

Original Papers