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.
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Additional information
Institute of Monocrystals, Academy of Sciences (NAN) of Ukraine, Khar'kov 310001. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1466–1471, November, 1997.
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Patsenker, L.D., Lokshin, A.I., Drushlyak, T.G. et al. Acylation of 5-phenyl-2-(fur-2-yl)oxazole. Chem Heterocycl Compd 33, 1266–1271 (1997). https://doi.org/10.1007/BF02320325
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DOI: https://doi.org/10.1007/BF02320325