Proceedings of the Steklov Institute of Mathematics.
Vol. 284.
2014.
P. 133-147
New heterocyclic systems based on substituted 3,4-dihydro-1H-spiro[quinoline-2,1'-cycloalkanes]
The Stollé type reaction of 3,4-dihydro-1H-spiro[quinoline-2,1'-cycloalkane] hydrochlorides with oxalyl chloride gave 6-methyl-5,6-dihydrospiro[pyrrolo[3,2,1-ij]quinoline-4,1'-cycloalkane]-1,2-diones, which were used in cyclocondensation with various 1,2- and 1,3-dinucleophiles and in a three-component cyclocondensation with malononitrile (or ethyl cyanoacetate) and several carbonyl compounds with activated methylene group. © 2014 Springer Science+Business Media New York.
Authors
Medvedeva S.M.1
,
Krysin M.Y.1
,
Zubkov F.I.
2
,
Nikitina E.V.
2
,
Shikhaliev K.S.1
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
9
Language
English
Pages
1280-1290
Status
Published
Link
Volume
50
Year
2014
Organizations
- 1 Voronezh State University, 1 Universitetskaya Sq., Voronezh, 394006, Russian Federation
- 2 Peoples' Friendship University of Russia, 6 Miklukho-Maklaya St., Moscow, 117198, Russian Federation
Keywords
1 2-dinucleophiles; 1 3-dinucleophiles; 3 4-dihydro-1H-spiro[quinoline-2 1-cycloalkanes]; 6-methyl-5 6-dihydrospiro[pyrrolo[3 2 1-ij]quinoline-4 1-cycloalkane]-1 2-diones; cyclocondensation; oxalyl chloride; Stollé reaction; three-component cyclocondensation
Date of creation
19.10.2018
Date of change
13.08.2021
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Other records
Current Medical Research and Opinion.
Vol. 30.
2014.
P. 805-811