Substituted 2- and 4-benzylpyridines in the synthesis of benzo[g]quinolines and benzo[g]isoquinolines

Nitrogen-containing heterocyclic analogs of anthracene, viz., benzo[g]isoquinolines and benzo[g]quinolines, were obtained by dehydrocyclization on a K-16 catalyst of mixtures of methyl-substituted 2- and 4-benzylpyridines with methyl groups in various positions of the pyridine and benzyl rings, which are formed by benzylation of β-picoline, as well as pyridine, by the Ladenburg method. The spectral characteristics of the synthesized compounds are presented. © 1980 Plenum Publishing Corporation.

Authors
Prostakov N.S. 1 , Kuznetsov V.I. 1 , Datta Rai G.
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
5
Language
English
Pages
525-529
Status
Published
Volume
16
Year
1980
Organizations
  • 1 P. Lumumba International-Friendship University, Moscow, 117923, Russian Federation
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