Indexed keywords
ARYLATIONS;
CARBON-CARBON BOND FORMATION;
ELECTRON-RICH ARENES;
FRIEDEL-CRAFTS;
CHEMICAL REACTIONS;
AROMATIC COMPOUNDS;
BENZOXAZINE DERIVATIVE;
METHYL 2 [2 (2 HYDROXY 5 METHYLPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [2 (2 HYDROXY 5 METHYLPHENYL) 6 METHYL 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [2 (2 HYDROXY 5 METHYLPHENYL) 7 METHYL 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [2 (2,4 DIMETHOXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [2 (2,4 DIMETHOXYPHENYL) 6 METHYL 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [2 (2,4 DIMETHOXYPHENYL) 7 METHYL 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [2 (2,4,6 TRIMETHOXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [2 (3 HYDROXY 2,4 DIMETHOXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [2 (3 HYDROXY 2,4 DIMETHOXYPHENYL) 6 METHYL 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [2 (3 HYDROXY 2,4 DIMETHOXYPHENYL) 7 METHYL 2H BENZO[B][1,4]OXACIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [2 (3,5 DI TERT BUTYL 4 HYDROXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [2 (3,5 DI TERT BUTYL 4 HYDROXYPHENYL) 6 METHYL 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [2 (3,5 DI TERT BUTYL 4 HYDROXYPHENYL) 7 METHYL 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 BROMO 2 (2 HYDROXY 5 METHYLPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 BROMO 2 (2,4 DIMETHOXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 BROMO 2 (2,4,6 TRIMETHOXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 BROMO 2 (3 HYDROXY 2,4 DIMETHOXYPHENYL) 6 METHYL 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 BROMO 2 (3,5 DI TERT BUTYL 4 HYDROXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 CHLORO 2 (2 HYDROXY 5 METHYLPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 CHLORO 2 (2,4 DIMETHOXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 CHLORO 2 (2,4,6 TRIMETHOXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 CHLORO 2 (3 HYDROXY 2,4 DIMETHOXYPHENYL) 6 METHYL 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 CHLORO 2 (3,5 DI TERT BUTYL 4 HYDROXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 METHYL 2 (2,4,6 TRIMETHOXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 TERT BUTYL (3,5 DI TERT BUTYL 4 HYDROXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 TERT BUTYL 2 (2 HYDROXY 5 METHYLPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 TERT BUTYL 2 (2,4 DIMETHOXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [6 TERT BUTYLL 2 (2,4,6 TRIMETHOXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
METHYL 2 [7 METHYL 2 (2,4,6 TRIMETHOXYPHENYL) 2H BENZO[B][1,4]OXAZIN 3 (4H) YLIDENE]ACETATE;
UNCLASSIFIED DRUG;
ARTICLE;
ARYLATION;
CARBON NUCLEAR MAGNETIC RESONANCE;
COLUMN CHROMATOGRAPHY;
DRUG SYNTHESIS;
ELECTRON;
FRIEDEL CRAFTS REACTION;
INFRARED SPECTROSCOPY;
PROTON NUCLEAR MAGNETIC RESONANCE;
THIN LAYER CHROMATOGRAPHY;
X RAY ANALYSIS;
2
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