caa a22 4500 467993343 CHVBK 20180323112551.0 cr unu---uuuuu 170328e19900501xx s 000 0 eng 10.1007/BF00487425 doi (NATIONALLICENCE)springer-10.1007/BF00487425 Rearrangement of 1-acetylindoxyl oxime to 1-acetyl-2-chloro-3-iminoindoline hydrochloride [Elektronische Daten] [V. Velezheva, S. Ryabova] Rearrangement of 1-acetylindoxyl oxime upon treatment with hydrogen chloride in acetic acid results in the formation of 1-acetyl-2-chloro-3-iminoindoline hydrochloride. Hydrolysis and acylation of the latter have been studied, along with reaction of 1-acetyl-2-chloro-3-(Ω-chloroacetyl)aminoindole with N- and S-nucleophiles. Plenum Publishing Corporation, 1990 Velezheva V. S. Ordzhonikidze All-Union Scientific Research Chemical Pharmaceutical Institute, Moscow aut Ryabova S. S. Ordzhonikidze All-Union Scientific Research Chemical Pharmaceutical Institute, Moscow aut Chemistry of Heterocyclic Compounds Kluwer Academic Publishers-Plenum Publishers 26/5(1990-05-01), 520-524 0009-3122 26:5<520 1990 26 10593 https://doi.org/10.1007/BF00487425 text/html Onlinezugriff via DOI 1 research-article jats NATIONALLICENCE 856 40 https://doi.org/10.1007/BF00487425 text/html Onlinezugriff via DOI NATIONALLICENCE 700 1- Velezheva V. S. Ordzhonikidze All-Union Scientific Research Chemical Pharmaceutical Institute, Moscow aut NATIONALLICENCE 700 1- Ryabova S. S. Ordzhonikidze All-Union Scientific Research Chemical Pharmaceutical Institute, Moscow aut NATIONALLICENCE 773 0- Chemistry of Heterocyclic Compounds Kluwer Academic Publishers-Plenum Publishers 26/5(1990-05-01), 520-524 0009-3122 26:5<520 1990 26 10593 Metadata rights reserved Springer special CC-BY-NC licence nationallicence SWISSBIB 467992118 BK010053 XK010053 XK010000 NATIONALLICENCE NATIONALLICENCE NL-springer