BROMINATION OF 3-ACYL-2-AMINOINDOLES

DOI: 10.1007/BF00497213

Source and publish data:

Chemistry of Heterocyclic Compounds p. 416 - 420 (1990)

Update date:2022-07-29

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Authors:

Golubeva, G. A.

Sviridova, L. A.

Besidskii, E. S.

Besidskaya, G. S.

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Article abstract of DOI:10.1007/BF00497213

Unlike 3-acylindoles, 3-acyl-2-aminoindoles display high selectivity on being electrophilically attacked in the benzene ring , and are substituted at the 6-position.At the same time, an unco-substitution of the acyl group takes place (to the greatest exte

Full text of DOI:10.1007/BF00497213

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