A New Method for the Synthesis of Substituted 8,9,10,11-Tetrahydroindolo[1,2-a]Quinoxalin-6(5H)-Ones

Autor:	E. A. Khafizova, Il'dar Kh. Rizvanov, Dmitry B. Krivolapov, Vakhid A. Mamedov, Anastasiya I. Zamaletdinova, Oleg G. Sinyashin, Julia K. Voronina, Ekaterina V. Mironova, Saniya F. Kadyrova
Rok vydání:	2017
Předmět:	Stork enamine alkylation Annulation Tandem 010405 organic chemistry Chemistry Stereochemistry Intramolecular force Organic Chemistry Dehydrogenation 010402 general chemistry 01 natural sciences 0104 chemical sciences Sequence (medicine)
Zdroj:	Chemistry of Heterocyclic Compounds. 53:560-567
ISSN:	1573-8353 0009-3122
Popis:	The reaction of 1-(cyclohexen-1-yl)pyrrolidines with 3-(α-chlorobenzyl)quinoxalin-2(1H)-ones resulted in the formation of 8,9,10,11-tetrahydroindolo[1,2-a]quinoxalin-6(5H)-ones via a tandem sequence of Stork enamine alkylation and intramolecular annulation. Oxidative dehydrogenation gave indolo[1,2-a]quinoxalin-6(5H)-one.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::f5cdd4c464bd29d358270c1247b9be78 https://doi.org/10.1007/s10593-017-2090-0 Zobrazit plný text záznamu Plný text ve formátu PDF