Abstract:Die aromatischen Halogenverbindungen (I) reagieren mit Trimethylsilylacetylen (II) in Gegenwart von Pd(II)‐Komp1exen wie (III) zu den Substitutionsprodukten (IV), die z.B. mit Methanol/Carbonat zu den Arylacetylenen Ff (V) gespalten werden.
“…The organics were washed twice with water and once with brine solution. The organics were dried over MgSO 4 , and the solvent and excess electrophiles were removed under reduced pressure to give a slightly viscous, yellow liquid.…”
Section: Reaction Of Allyl Chloride and Propargyl Bromide With Fluorenementioning
“…The organics were washed twice with water and once with brine solution. The organics were dried over MgSO 4 , and the solvent and excess electrophiles were removed under reduced pressure to give a slightly viscous, yellow liquid.…”
Section: Reaction Of Allyl Chloride and Propargyl Bromide With Fluorenementioning
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