iron (III) acetylacetonate; hydrazine hydrate in methanol T=150°C; Microwave irradiationGreen chemistry;

palladium diacetate; sodium carbonate in water; acetone T=35°C; 12 h;

sodium hydroxide in water T=75°C;

1: bis(4-chlorophenyl)borinic acid With sodium hydroxide in tetrahydrofuran; water T=20°C; 1 h; 2: With triphenylphosphine in tetrahydrofuran; water T=20°C; 0.5 h; 3: 1-Bromo-2-aminobenzene With hydrogenchloride; palladium dichloride in tetrahydrofuran; water T=100°C; P=2625.26 Torr; 12 h;

1: para-dichlorobenzene With magnesium; ethylene dibromide; lithium chloride in tetrahydrofuran T=25°C; Negishi coupling reaction; 0.5 h; 2: With zinc(II) chloride in tetrahydrofuran T=25°C; Negishi coupling reaction; 0.5 h; 3: 1-Bromo-2-aminobenzene With dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine; palladium diacetate in tetrahydrofuran T=25°C; Negishi coupling reaction; 3 h;

10 palladium on activated carbon; hydrogen in methanol T=40°C; P=37503.8 Torr;

1: With dihydrogen peroxide; sodium hydroxide in ethanol; water 2: With sodium hypochlorite; sodium hydroxide in ethanol; water Hofmann rearrangement;

sodium methylate in 1,4-dioxane T=100°C; Suzuki-Miyaura Coupling; 25 h; Schlenk technique;

oxygen; sodium hydroxide in water T=60°C; 33 h; regioselective reaction;

manganese(IV) oxide in acetonitrile T=20°C; Overall yield = 54 percent; regioselective reaction;