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.

Авторы
Medvedeva S.M.1 , Krysin M.Y.1 , Zubkov F.I. 2 , Nikitina E.V. 2 , Shikhaliev K.S.1
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
9
Язык
Английский
Страницы
1280-1290
Статус
Опубликовано
Том
50
Год
2014
Организации
  • 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
Ключевые слова
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
Дата создания
19.10.2018
Дата изменения
13.08.2021
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/4963/
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