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.

Authors
Nadein O.N.1 , Aksenov D.А.1 , Abakarov G.M.2 , Aksenov N.А.1 , Voskressensky L.G. 3 , Aksenov A.V. 1
Editors
-
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
10
Language
English
Pages
905-932
Status
Published
Department
-
Number
-
Volume
55
Year
2019
Organizations
  • 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
Keywords
annulation; cryptolepine; cryptosanguinolentine; cryptotackieine; heteroannulation; indoloquinolines; isocryptolepine; isoneocryptolepine; neocryptolepine; polycyclic indoles; polyheteroindoles; quindoline
Date of creation
24.12.2019
Date of change
24.12.2019
Short link
https://repository.rudn.ru/en/records/article/record/54987/