Acylation of 5-phenyl-2-(fur-2-yl)oxazole

Authors

  • Л. Д. Паценкер Institute of Monocrystals, Academy of Sciences (NAN) of Ukraine, Khar'kov 310001
  • А. И. Локшин Institute of Monocrystals, Academy of Sciences (NAN) of Ukraine, Khar'kov 310001
  • Т. Г. Друшляк Institute of Monocrystals, Academy of Sciences (NAN) of Ukraine, Khar'kov 310001
  • B. Н. Баyмер Institute of Monocrystals, Academy of Sciences (NAN) of Ukraine, Khar'kov 310001

Abstract

The ability of 5-phenyl-2-(fur-2-yl)oxazole to undergo acetylation and formylation is considered. It was established by X-ray structure analysis that electrophilic substitution proceeds at the position 5 of the furan ring. The direction of the reactions is analyzed from positions of the energy preference of transition states.

How to Cite
Patsenker, L. D.; Lokshin, A. I.; Drushlyak, T. G.; Baumer, V. N. Chem. Heterocycl. Compd. 1997, 33, 1266. [Khim. Geterotsikl. Soedin. 1997, 1466.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02320325

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Published

1997-11-25

Issue

No. 11 (1997)

Section

Original Papers