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Volumn 60, Issue 44, 2004, Pages 9953-9961
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Reaction of 3-aminoquinoline-2,4-diones with nitrourea. Synthetic route to novel 3-ureidoquinoline-2,4-diones and imidazo[4,5-c]quinoline-2,4-diones
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Author keywords
Aminoketones; Ureidoketones; Molecular rearrangement; Nitrourea; Urea derivatives
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Indexed keywords
1 BUTYL 2,6 DIHYDROIMIDAZO[1,5 C]QUINAZOLINE 3,5 DIONE;
1 PHENYL 2,6 DIHYDROIMIDAZO[1,5 C]QUINAZOLINE 3,5 DIONE;
1,2 DIBUTYL 2,6 DIHYDROIMIDAZO[1,5 C]QUINAZOLINE 3,5 DIONE;
2 BENZYL 1 BUTYL 2,6 DIHYDROIMIDAZO[1,5 C]QUINAZOLINE 3,5 DIONE;
2 BENZYL 1 PHENYL 2,6 DIHYDROIMIDAZO[1,5 C]QUINAZOLINE 3,5 DIONE;
2 BUTYL 1 PHENYL 2,6 DIHYDROIMIDAZO[1,5 C]QUINAZOLINE 3,5 DIONE;
3 BENZYL 3A BUTYL 3,3A DIHYDRO 5H IMIDAZO[4,5 C]QUINOLINE 2,4 DIONE;
3 BENZYL 3A BUTYL 9B HYDROXY 3,3A,5,9B TETRAHYDRO 1H IMIDAZO[4,5 C]QUINOLINE 2,4 DIONE;
3 BENZYL 3A PHENYL 3,3A DIHYDRO 5H IMIDAZO[4,5 C]QUINOLINE 2,4 DIONE;
3 BENZYL 9B HYDROXY 3A PHENYL 3,3A,5,9B TETRAHYDRO 1H IMIDAZO[4,5 C]QUINOLINE 2,4 DIONE;
3 BUTYL 3 UREIDO 1H,3H QUINOLINE 2,4 DIONE;
3 BUTYL 3A PHENYL 3,3A DIHYDRO 5H IMIDAZO[4,5 C]QUINOLINE 2,4 DIONE;
3 BUTYL 9B HYDROXY 3A PHENYL 3,3A,5,9B TETRAHYDRO 1H IMIDAZO[4,5 C]QUINOLINE 2,4 DIONE;
3,3A DIBUTYL 3,3A DIHYDRO 5H IMIDAZO[4,5 C]QUINOLINE 2,4 DIONE;
3,3A DIBUTYL 9B HYDROXY 3,3A,5,9B TETRAHYDRO 1H IMIDAZO[4,5 C]QUINOLINE 2,4 DIONE;
9B HYDROXY 3A PHENYL 3,3A,5,9B TETRAHYDRO 1H IMIDAZO[4,5 C]QUINOLINE 2,4 DIONE;
AMINOQUINOLINE DERIVATIVE;
IMIDAZOQUINOLINE DERIVATIVE;
QUINOLINE DERIVATIVE;
UNCLASSIFIED DRUG;
UREA DERIVATIVE;
ANALYTIC METHOD;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CHEMICAL PROCEDURES;
CHEMICAL REACTION;
COLUMN CHROMATOGRAPHY;
DRUG SYNTHESIS;
NITROGEN NUCLEAR MAGNETIC RESONANCE;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
REACTION ANALYSIS;
STRUCTURE ANALYSIS;
STAPHYLOCOCCUS PHAGE 3A;
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EID: 4644349893
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/j.tet.2004.07.106 Document Type: Article |
Times cited : (21)
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References (10)
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