Methods of synthesis of natural indoloquinolines isolated from Cryptolepis sanguinolenta

[Figure not available: see fulltext.] The review summarizes the approaches to the synthesis of natural biologically active indoloquinoline systems isolated from Cryptolepis sanguinolenta published over the past twenty years. The classification of the existing methods was carried out according to the principle of building of the heterocyclic system: annulation to an already existing indole or quinoline ring or tandem formation of both rings. © 2019, Springer Science+Business Media, LLC, part of Springer Nature.

Авторы
Nadein O.N.1 , Aksenov D.А.1 , Abakarov G.M.2 , Aksenov N.А.1 , Voskressensky L.G. 3 , Aksenov A.V. 1
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
10
Язык
Английский
Страницы
905-932
Статус
Опубликовано
Том
55
Год
2019
Организации
  • 1 North Caucasus Federal University, 1a Pushkina St., Stavropol, 355009, Russian Federation
  • 2 Dagestan State Technical University, 70 Imama Shamilya Ave., Makhachkala, Dagestan 367015, Russian Federation
  • 3 RUDN University, 6 Miklukho-Maklaya St., Moscow, 117198, Russian Federation
Ключевые слова
annulation; cryptolepine; cryptosanguinolentine; cryptotackieine; heteroannulation; indoloquinolines; isocryptolepine; isoneocryptolepine; neocryptolepine; polycyclic indoles; polyheteroindoles; quindoline
Дата создания
24.12.2019
Дата изменения
24.12.2019
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/54987/
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