Cyanoethylation of 3-methyl-2-azafluorene

3-Methyl-9,9-di(β-cyanoethyl)-2-azafluorene was obtained from 3-methyl-2-azafluorene via the Michael reaction and was converted to the dibasic acid and its diester. Dieckmann condensation of the latter and subsequent hydrolysis gave 3-methyl-4′-oxospiro(2-azafluorene-9,1′-cyclohexane). © 1974 Consultants Bureau, a division of Plenum Publishing Corporation.

Editors
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Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
12
Language
English
Pages
1513-1515
Status
Published
Department
-
Number
-
Volume
8
Year
1974
Organizations
  • 1 Patrice Lumumba University, Moscow, Russian Federation
Keywords
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Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/1791/