Cyanoethylation of azafluorenes and syntheses of alcohols containing an azafluorene fragment

Isomeric (with respect to the position of the nitrogen atom) azafluorenes were cyanoethylated. The resulting 9,9-bis(β-cyanoethyl) derivatives were converted to the corresponding dibasic acids and their diesters. The latter were subjected to the Dieckmann reaction to obtain spiro compounds with azafluorene and cyclohexene fragments. The analogous spirans with 1,3-dioxalane and 1,3-dioxane rings were obtained from 3-methyl-2-azafluorenone. © 1983 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
1290-1294
Status
Published
Department
-
Number
-
Volume
18
Year
1982
Organizations
  • 1 Patrice Lumumba People's Friendship University, Moscow, 117923, 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/1441/