Russian Chemical Bulletin

, Volume 57, Issue 7, pp 1539–1542

Functionalization of 4,6-dinitro-2-phenylindole at position 7

  • M. A. Bastrakov
  • A. M. Starosotnikov
  • A. Kh. Shakhnes
  • S. A. Shevelev
Full Articles

DOI: 10.1007/s11172-008-0198-1

Cite this article as:
Bastrakov, M.A., Starosotnikov, A.M., Shakhnes, A.K. et al. Russ Chem Bull (2008) 57: 1539. doi:10.1007/s11172-008-0198-1

Abstract

Transformation of the amino group in 7-amino-1-methyl-4,6-dinitro-2-phenylindole afforded a number of new 7-R-4,6-dinitroindoles and a first representative of a novel tricyclic heteroaromatic system of [1,2,5]oxadiazolo[4,3-g]indole.

Key words

indolesnitro compoundsamino groupdiazotizationnucleophilic substitution

Copyright information

© Springer Science+Business Media, Inc.  2008

Authors and Affiliations

  • M. A. Bastrakov
    • 1
  • A. M. Starosotnikov
    • 1
  • A. Kh. Shakhnes
    • 1
  • S. A. Shevelev
    • 1
  1. 1.N. D. Zelinsky Institute of Organic ChemistryRussian Academy of SciencesMoscowRussian Federation