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首页> 外文期刊>Chemistry - A European Journal >Palladium-Catalyzed Cross-Coupling Reactions of Organogold(I) Reagents with Organic Electrophiles
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Palladium-Catalyzed Cross-Coupling Reactions of Organogold(I) Reagents with Organic Electrophiles

机译:钯催化有机金(I)试剂与有机亲电试剂的交叉偶联反应

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摘要

The palladium-catalyzed cross-coupling reaction of organogold(I) reagents (alkyl, alkenyl, aryl, and alkynyl) with organic electrophiles, such as aryl and alkenyl halides, aryl triflates, benzyl bromide, and benzoyl chloride is reported. The reaction takes place, under palladium catalysis, at room temperature with short reaction times to give the corresponding cross-coupling products in high yields.
机译:据报道,有机金(I)试剂(烷基,烯基,芳基和炔基)与有机亲电子试剂(如芳基和烯基卤化物,芳基三氟甲磺酸酯,苄基溴和苯甲酰氯)的钯催化交叉偶联反应。该反应在钯催化下于室温下以短反应时间进行,从而以高收率得到相应的交叉偶联产物。

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