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2), 5.59 (1H, s, Ar-CH), 6.58-6.59 (1H, m, ArH), 6.68
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2 (136 mg, 1 mmol) or (b) anhydrous aluminum chloride (133 mg, 1 mmol) were successively added and heated in the oil bath at 140 C for 5 h. The product was isolated from the reaction mixture as stated in 3-diarylmethyl indole synthesis above. (a) Yield = 176 mg (54%) (b) Yield = 232 mg (71%).
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Representative Procedure for 3-diarylmethyl Indole Synthesis
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