Abstract
The transformation of propionic acid N,N-diarylhydrazides with electron-donor and electron-acceptor substituents in the aromatic rings under the conditions of the Kost reaction was studied. The ratios of the resulting isomeric N-aryl-2-aminoindoles were determined.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1213–1217, September, 1985.
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Barinova, V.N., Voronin, V.G., Zhestkov, V.P. et al. Regioselectivity of the rearrangement of propionic acid N,N-diarylhydrazides under the conditions of the kost reaction. Chem Heterocycl Compd 21, 1008–1012 (1985). https://doi.org/10.1007/BF00515024
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DOI: https://doi.org/10.1007/BF00515024