Reaction of 1-substituted 3-aminoquinoline-2,4-diones with isothiocyanates. An easy pathway to generate novel 2-thioxo-1′H-spiro[imidazoline-5,3′-indole]-2,2′-diones

Tetrahedron

Volumn 65, Issue 25, 2009, Pages 4908-4916

  Klásek, Antonín ^a   Mrkvička, Vladimír ^a   Lyčka, Antonín ^b,c   Mikšík, Ivan ^c,d   Růžička, Aleš ^e  

^a TOMAS BATA UNIVERSITY IN ZLIN   (Czech Republic)

^b Vyzkumny ustav organickych syntez as   (Czech Republic)

^c UNIVERSITY OF HRADEC KRALOVE   (Czech Republic)

^d INSTITUTE OF PHYSIOLOGY   (Czech Republic)

^e UNIVERSITY OF PARDUBICE   (Czech Republic)

Author keywords

Aminoketones; Enamides; Rearrangement; Spiro heterocycles; Thiourea derivatives

Indexed keywords

ACETIC ACID; HYDROCHLORIC ACID; HYDROGEN; IMIDAZOLINE DERIVATIVE; ISOTHIOCYANIC ACID; QUINOLINE DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CRYSTAL STRUCTURE; INFRARED RADIATION; MASS SPECTROMETRY; NITROGEN NUCLEAR MAGNETIC RESONANCE; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; REACTION ANALYSIS; SUBSTITUTION REACTION; X RAY DIFFRACTION;

EID: 65549140188     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.04.009     Document Type: Article

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