caa a22 4500 467992754 CHVBK 20180323112549.0 cr unu---uuuuu 170328e19900401xx s 000 0 eng 10.1007/BF00497213 doi (NATIONALLICENCE)springer-10.1007/BF00497213 Bromination of 3-acyl-2-aminoindoles [Elektronische Daten] [G. Golubeva, L. Sviridova, E. Besidskii, G. Besidskaya] 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-subsitution of the acyl group takes place (to the greatest extent — the formyl group). Direct bromination of 3-acyl- and 3-cyano-2-aminoindoles provides the 6-bromo- and 6,4-dibromo-2-aminoindoles and their derivatives. Plenum Publishing Corporation, 1990 Golubeva G. M. V. Lomonsov State University, 119899, Moscow aut Sviridova L. M. V. Lomonsov State University, 119899, Moscow aut Besidskii E. M. V. Lomonsov State University, 119899, Moscow aut Besidskaya G. M. V. Lomonsov State University, 119899, Moscow aut Chemistry of Heterocyclic Compounds Kluwer Academic Publishers-Plenum Publishers 26/4(1990-04-01), 416-420 0009-3122 26:4<416 1990 26 10593 https://doi.org/10.1007/BF00497213 text/html Onlinezugriff via DOI 1 research-article jats NATIONALLICENCE 856 40 https://doi.org/10.1007/BF00497213 text/html Onlinezugriff via DOI NATIONALLICENCE 700 1- Golubeva G. M. V. Lomonsov State University, 119899, Moscow aut NATIONALLICENCE 700 1- Sviridova L. M. V. Lomonsov State University, 119899, Moscow aut NATIONALLICENCE 700 1- Besidskii E. M. V. Lomonsov State University, 119899, Moscow aut NATIONALLICENCE 700 1- Besidskaya G. M. V. Lomonsov State University, 119899, Moscow aut NATIONALLICENCE 773 0- Chemistry of Heterocyclic Compounds Kluwer Academic Publishers-Plenum Publishers 26/4(1990-04-01), 416-420 0009-3122 26:4<416 1990 26 10593 Metadata rights reserved Springer special CC-BY-NC licence nationallicence BK010053 XK010053 XK010000 NATIONALLICENCE NATIONALLICENCE NL-springer