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Palladium-Catalyzed Reaction of 2-Hydroxy-2-methylpropiophenone with Aryl Bromides: A Unique Multiple Arylation via Successive C−C and C−H Bond Cleavages

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https://figshare.com/articles/dataset/Palladium_Catalyzed_Reaction_of_2_Hydroxy_2_methylpropiophenone_with_Aryl_Bromides_A_Unique_Multiple_Arylation_via_Successive_C_C_and_C_H_Bond_Cleavages/3331576
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2-Hydroxy-2-methylpropiophenone undergoes a unique multiple arylation via C−C and C−H bond cleavages upon treatment with excess aryl bromides in the presence of a palladium catalyst to give 1,1,2,2-tetraarylethanes and 4,4-diaryl-1-phenylisochroman-3-ones.
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2016-05-06
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