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首页> 外文期刊>European journal of organic chemistry >Synthesis of 2′,4-diarylbenzophenones through site-selective suzuki-miyaura reactions of bis(triflates) of 2′,4-dihydroxybenzophenones
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Synthesis of 2′,4-diarylbenzophenones through site-selective suzuki-miyaura reactions of bis(triflates) of 2′,4-dihydroxybenzophenones

机译:通过2',4-二羟基二苯甲酮双(三氟甲磺酸酯)的位点选择性铃木-宫浦反应合成2',4-二芳基二苯甲酮

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摘要

Palladium(0)-catalyzed Suzuki cross-coupling reactions of the bis(triflates) of 2′,4-dihydroxybenzophenones afforded 2′,4-diarylbenzophenones. The reactions proceeded with very good site selectivity in favour of the 4-position. Palladium(0)-catalyzed Suzuki cross-coupling reactions of the bis(triflates) of 2′,4- dihydroxybenzophenones afforded 2′,4-diarylbenzophenones. The reactions proceeded with very good site selectivity infavour of the 4-position.
机译:2',4-二羟基二苯甲酮的双(三氟甲磺酸酯)的钯(0)催化的Suzuki交叉偶联反应得到2',4-二芳基二苯甲酮。反应以有利于4-位的非常好的位点选择性进行。 2',4-二羟基二苯甲酮的双(三氟甲磺酸酯)的钯(0)催化的Suzuki交叉偶联反应得到2',4-二芳基二苯甲酮。反应以4-位非常好的位点选择性进行。

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