Synthesis of spiro analogs of lilolidine alkaloids

The Friedel-Krafts intramolecular cyclization of N-chloroacetyl- and N-α-bromopropionyl-4-methylspiro[tetrahydroquinoline-2-cyclohexanes] was used to obtain 2-oxo-1,2,5,6-tetrahydro-4H-spiro[pyrrolo(3,2,1-i,j)quinoline-4,1′-cyclohexanes]- spiro analogs of lilolidine alkaloids. © 1994 Plenum Publishing Corporation.

Authors
Kuznetsov V.V. 1 , Pal'ma A.R. 1 , Prostakov N.S. 1 , Varlamov A.V. 1
Journal
Chemistry of Heterocyclic Compounds
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
11
Language
English
Pages
1296-1299
Status
Published
Link
External link
DOI
10.1007/BF00532028
Volume
29
Year
1993
Organizations
  • 1 Russian University of People's 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/977/
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