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Typical procedure: To a solution of 2 (0.75 mmol, 6a (0.5mmol, and TEA (3.0mmol) in CH2Cl2 (5 ml) was added Cu(OAc)2 (0.55 mmol, and the mixture was stirred for 6h at 40°C (bath temperature, The mixture was diluted with CH2Cl2 (50 ml) and NH3 aq, 1.5mol/l, 50 ml) and then stirred for 30min. The organic layer was separated, washed with brine and dried over anhydrous MgSO4. After removal of the solvent in vacuo, the residue was separated by SiO2 column chromatography (hexane: CH 2Cl2=3 :1) to give 7a 77 mg, 84% yield
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2=3 :1) to give 7a (77 mg, 84% yield).
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The tetraarylantimony acetates (2, 10, 11) were prepared by dis-proportination reaction on heating 1 :1 mixture of Ar 5Sb and Ar3Sb(OAc)2 in toluene (100 °C) for 3-6h. 2: (C6H5)4SbOAc, mp 135-136°C (lit.37) 129-131 °C, 10: (4-CH3C 6H4)4SbOAc, mp 160-163 °C (lit. 38) 157-158.1 °C, 11: (4-ClC6H4) 4SbOAc, mp 184-187°C
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4SbOAc, mp 184-187°C.
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