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10744226592
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For an example of aryne-type aminations of chloropyridines see:
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For an example of aryne-type aminations of chloropyridines see: Sun Q., Tafesse L., Islam K., Zhou X.M., Victory S.F., Zhang C.W., Hachicha M., Schmid L.A., Patel A., Rotshteyn Y., Valenzano K.J., Kyle D.J. Bioorg. Med. Chem. Lett. 13:2003;3611-3616.
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38
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85030907135
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note
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2 (1 mol %), ligand (2 mol %), N-benzylpiperazine (1.5 mmol), (hetero)aryl halide (1.25 mmol), and hexadecane (100 μL; as internal standard for GC) were transferred subsequently from inert stock solutions (anhydrous toluene) and diluted with anhydrous toluene (total volume of toluene: 3 mL). The reactor was kept shaking with 350 rpm over 20 h at 110 °C. After cooling to rt and automatical filtration using a cleavage block, reaction mixtures were removed from reactor, analyzed by GC and/or chromatographed on silica using eluent mixtures of hexane/ethyl acetate in different ratios. The identity of the products was confirmed by GC-MS and NMR data.
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39
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0001211425
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Commercially available at Strem or Degussa Homogeneous Catalysts;
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Zapf, A.1
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Heinrich, T.7
Böttcher, H.8
Beller, M.9
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