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
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/740/