Indexed keywords
CHEMISTRY;
DIVERSITY-ORIENTED SYNTHESIS;
ONE-POT PROTOCOL;
POLYHETEROCYCLES;
SALIENT FEATURES;
ORGANIC COMPOUNDS;
(3 BROMOINDOLO[1,2 A]QUINOXALIN 6 YL)[4 (TERT BUTYL)PHENYL]METHANONE;
(3 METHYLINDOLO[1,2 A]QUINOXALIN 6 YL)(PHENYL)METHANONE;
(9 CHLOROINDOLO[1,2 A]QUINOXALIN 6 YL)(4 TOLYL)METHANONE;
(9,10 DIMETHOXYINDOLO[1,2 A]QUINOXALIN 6 YL)(PHENYL)METHANONE;
(INDOLO[1,2 A]QUINOXALIN 6 YL)(PHENYL)METHANONE;
(PHENYL)[3 (TRIFLUOROMETHYL)INDOLO[1,2 A]QUINOXALIN 6 YL]METHANONE;
([1,3]DIOXOLO[4',5':5,6]INDOLO[1,2 A]QUINOXALIN 6 YL)(PHENYL)METHANONE;
([1,3]DIOXOLO[4',5':5,6]INDOLO[1,2 A]QUINOXALIN-6-YL)[4 (TERT BUTYL)PHENYL]METHANONE;
1 PHENYL 6 (TRIFLUOROMETHYL)INDOLO[1,2 A][1,2,3]TRIAZOLO[5,1 C]QUINOXALINE;
1 PHENYLINDOLO[1,2 A][1,2,3]TRIAZOLO[5,1 C]QUINOXALINE;
1 [4 (TERT BUTYL)PHENYL] 11,12 DIMETHOXYINDOLO[1,2 A][1,2,3]TRIAZOLO[5,1 C]QUINOXALINE;
1 [4 (TERT BUTYL)PHENYL] 6 (TRIFLUOROMETHYL)INDOLO[1,2 A][1,2,3]TRIAZOLO[5,1 C]QUINOXALINE;
1 [4 (TERT BUTYL)PHENYL]INDOLO[1,2 A][1,2,3]TRIAZOLO[5,1 C]QUINOXALINE;
1 [4 (TERT BUTYL)PHENYL][1,3]DIOXOLO[4',5':5,6]INDOLO[1,2 A][1,2,3]TRIAZOLO[5,1 C]QUINOXALINE;
11,12 DIMETHOXY 1 PHENYL 6 (TRIFLUOROMETHYL)INDOLO[1,2 A][1,2,3]TRIAZOLO[5,1 C]QUINOXALINE;
12 CHLORO 1 (4 TOLYL)INDOLO[1,2 A][1,2,3]TRIAZOLO[5,1 C]QUINOXALINE;
6 BROMO 1 [4 (TERT BUTYL)PHENYL]INDOLO[1,2 A][1,2,3]TRIAZOLO[5,1 C]QUINOXALINE;
6 BROMO 12 CHLORO 1 (4 TOLYL)INDOLO[1,2 A][1,2,3]TRIAZOLO[5,1 C]QUINOXALINE;
6 FLUORO 1 PHENYLINDOLO[1,2 A][1,2,3]TRIAZOLO[5,1 C]QUINOXALINE;
6 FLUORO 1 PHENYL[1,3]DIOXOLO[4',5':5,6]INDOLO[1,2 A][1,2,3]TRIAZOLO[5,1 C]QUINOXALINE;
INDOLE DERIVATIVE;
INDOLOTRIAZOLOQUINOXALINE DERIVATIVE;
KETOINDOLOQUINOXALINE DERIVATIVE;
QUINOXALINE DERIVATIVE;
UNCLASSIFIED DRUG;
[4 (TERT BUTYL)PHENYL](3 FLUOROINDOLO[1,2 A]QUINOXALIN 6 YL)METHANONE;
[4 (TERT BUTYL)PHENYL](9,10 DIMETHOXYINDOLO[1,2 A]QUINOXALIN 6YL)METHANONE;
[4 (TERT BUTYL)PHENYL](INDOLO[1,2 A]QUINOXALIN 6 YL)METHANONE;
AMINOOXYGENATION;
ANNULATION REACTION;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CATALYSIS;
CHEMICAL MODIFICATION;
CHEMICAL REACTION;
CYCLIZATION;
CYCLOADDITION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
PROTON NUCLEAR MAGNETIC RESONANCE;
SUBSTITUTION REACTION;
CATALYSIS;
CYCLOADDITION REACTION;
HETEROCYCLIC COMPOUNDS WITH 4 OR MORE RINGS;
INDOLES;
QUINOXALINES;
1
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The CCDC file 958098 (2a) contains supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
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