Synthesis, structure, and biological activity of [2.2]paracyclophanes. 6. Synthesis of 2-([2.2]paracyclophan-4-yl)(benzo[g])indoles

Cyclocondensation of 2-([2.2]paracyclophan-4-yl)-2-oxoethyltriethylammonium bromide with aniline and α-naphthylamine gives 2-(paracyclophan-4-yl)indoles and benzo[g]indole respectively. ©1998 Plenum Publishing Corporation.

Authors
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
8
Language
English
Pages
929-932
Status
Published
Volume
33
Year
1997
Organizations
  • 1 Russian University of National Friendship, Moscow 117198, Russian Federation
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