Electrophilic substitution of 1-methylindeno-1H-[2,1-b]pyridine

It is shown that electrophilic substitution of 1-methylindeno-1H-[2,1-b]pyridine takes place at the C9 atom in the case of acylation (acetylation, benzoylation, and formylation), bromination, and nitration. Data from the 13C NMR spectrum of this pseudoazulene confirm sp2 hybridization of the C9 atom. © 1983 Plenum Publishing Corporation.

Authors
Prostakov N.S. 1 , Soldatenkov A.T. 1 , Bagdadi M.V. 1 , Fomichev A.A. 1 , Golovtsov N.I. 1
Journal
Chemistry of Heterocyclic Compounds
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
9
Language
English
Pages
954-956
Status
Published
Link
External link
DOI
10.1007/BF00513440
Volume
18
Year
1982
Organizations
  • 1 Patrice Lumumba Peoples' Friendship University, Moscow, 117923, Russian Federation
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/1449/
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Other records

N-OXIDES OF 2- AND 4-AZAFLUORENONES AND NITRO DERIVATIVES OF 2- AND 4-AZAFLUORENES

Article
Prostakov N.S., Shendrik I.V., Anisimov B.N., Varlamov A.V., Fomichev A.A., Lavani-Édogiaverie S.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 18. 1982. P. 1085-1088