A facile route to imidazo[1,2-a]quinolines via a domino reaction

Synthesis

Volumn , Issue 10, 2008, Pages 1535-1540

  Iminov, Rustam T ^a   Tverdokhlebov, Anton V ^b   Tolmachev, Andrey A ^b   Volovenko, Yulian M ^a   Kostyuk, Alexander N ^c   Chernega, Alexander N ^c   Rusanov, Eduard B ^c  

^a TARAS SHEVCHENKO NATIONAL UNIVERSITY OF KYIV   (Ukraine)

^b ENAMINE LTD   (Ukraine)

^c INSTITUTE OF ORGANIC CHEMISTRY   (Ukraine)

Author keywords

Cyclizations; Domino reactions; Heterocycles; Imidazo 1,2 a quinolines; Nitriles

Indexed keywords

ACETONITRILE; REACTION KINETICS;

ACETONITRILES; BENZOXAZINE; DOMINO REACTIONS;

MICROFLUIDICS;

1 (2 OXOPROPYL) 2H 3,1 BENZOXAZINE 2,4 (1H) DIONE; 1, (3,3 DIMETHYL 2 OXOBUTYL); 2 METHYLIMIDAZO[1,2 A]QUINOLIN 5(3H) ONE; ACETIC ACID; ACETONITRILE; BENZOXAZINE DERIVATIVE; IMIDAZO[1,2 A]QUINOLINE; IMIDAZO[1,2 A]QUINOLINE 2,5(1H,3H) DIONE; METHYL 2,4 DIOXO 2H 3,1 BENZOXAZINE 1 (4H) ACETATE; QUINOLINE DERIVATIVE;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL INTERACTION; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; ISOLATION PROCEDURE; X RAY CRYSTALLOGRAPHY;

EID: 44949157818     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1072572     Document Type: Article

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