Publikace detail

Reaction of 1-Alkyl/aryl-3-Amino-1H,3H-quinoline-2,4-diones with Urea. Synthetic Route to Novel 3-Amino-1,3-dihydro-2H-indol-2-ones, 1H-spiro[imidazolidine-5,3´-indole]-2,2´-diones, and 3,3a-dihydro-5H-imidazo[4,5-c]quinoline-2,4-diones

Autoři: Klásek A. | Kořistek K. | Lyčka A. | Holčapek Michal

Rok: 2003

Druh publikace: článek v odborném periodiku

Název zdroje: Tetrahedron

Název nakladatele: Pergamon-Elsevier Science Ltd.

Místo vydání: Oxford

Strana od-do: 5279-5288

Tituly:

Jazyk	Název	Abstrakt	Klíčová slova
cze	Reaction of 1-Alkyl/aryl-3-Amino-1H,3H-quinoline-2,4-diones with Urea. Synthetic Route to Novel 3-Amino-1,3-dihydro-2H-indol-2-ones, 1H-spiro[imidazolidine-5,3´-indole]-2,2´-diones, and 3,3a-dihydro-5H-imidazo[4,5-c]quinoline-2,4-diones	Reaction of 1-Alkyl/aryl-3-Amino-1H,3H-quinoline-2,4-diones with Urea. Synthetic Route to Novel 3-Amino-1,3-dihydro-2H-indol-2-ones, 1H-spiro[imidazolidine-5,3´-indole]-2,2´-diones, and 3,3a-dihydro-5H-imidazo[4,5-c]quinoline-2,4-diones.	molecular rearrangement, urea derivatives, -aminoketones, reaction mechanism, NMR, MS
eng	Reaction of 1-Alkyl/aryl-3-Amino-1H,3H-quinoline-2,4-diones with Urea. Synthetic Route to Novel 3-Amino-1,3-dihydro-2H-indol-2-ones, 1H-spiro[imidazolidine-5,3´-indole]-2,2´-diones, and 3,3a-dihydro-5H-imidazo[4,5-c]quinoline-2,4-diones	Reaction of 1-Alkyl/aryl-3-Amino-1H,3H-quinoline-2,4-diones with Urea. Synthetic Route to Novel 3-Amino-1,3-dihydro-2H-indol-2-ones, 1H-spiro[imidazolidine-5,3´-indole]-2,2´-diones, and 3,3a-dihydro-5H-imidazo[4,5-c]quinoline-2,4-diones.	molecular rearrangement, urea derivatives, -aminoketones, reaction mechanism, NMR, MS

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