[N-butylthiazolium][Br] T=200 - 220°C; 0.0416667 h; Microwave irradiationInert atmosphere; TemperatureTime;

1: (3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)bis(naphthalen-2-ylmethyl)phenylgermane With Cu(BF4)2 in methanol; acetonitrile 2 h; Irradiation; 2: 4-bromo-1-benzyloxybenzene With copper(l) iodide; tetrabutyl ammonium fluoride; tris-(o-tolyl)phosphine; dichloro bis(acetonitrile) palladium(II) in N,N-dimethyl-formamide T=120°C; 16 h; Further stages.;

potassium tert-butylate; 1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-3-ol T=20 - 110°C; 48 h; Schlenk techniqueInert atmosphere;

NiCl2[(4-MeOPh)3P]2; K3PO4*3H2O; tris(4-methoxyphenyl)-phosphine in toluene T=110°C; 10 h; Inert atmosphere;

potassium phosphate; Ni(PCy3)2Cl2; tri-cyclo-hexyl-phosphine in 1,4-dioxane T=80°C; Suzuki cross-coupling; 14 h;

caesium carbonate in N,N-dimethyl-formamide T=23°C; Alkylation; 1 h;

trifluorormethanesulfonic acid in 1,4-dioxane T=20°C; 6 h; Inert atmosphere;

magnesium oxide in α,α,α-trifluorotoluene T=80°C; 24 h;

triphenyl phosphite; K3PO4*3H2O; Ipr.HCl; palladium diacetate in tert-butyl alcohol T=80°C; 12 h; Inert atmosphere; Reagent/catalystSolventTemperature;

sodium carbonate in ethanol; water T=20°C; Suzuki Coupling; Green chemistry;