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首页> 外文期刊>Angewandte Chemie >Palladium(0)-Catalyzed Intermolecular Carbocyclization of (1,n)-Diynes and Bromophenols: An Efficient Route to Tricyclic Scaffolds
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Palladium(0)-Catalyzed Intermolecular Carbocyclization of (1,n)-Diynes and Bromophenols: An Efficient Route to Tricyclic Scaffolds

机译:钯(0)催化的(1,n)-二炔和溴酚的分子间碳环化:一种有效的途径到三环支架。

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摘要

A novel palladium(0)-catalyzed dearomative cyclization reaction of bromophenols with (1,n)-diynes has been developed for building two new types of tricyclic architectures containing a quaternary carbon center. This method employs inexpensive bromophenols, and easily accessible tethered diynes. It exhibits a broad substrate scope and tolerates various functional groups. Preliminary results with commercially available chiral ligands indicate that enantioselective variants are feasible for both cyclization processes.
机译:一种新型的钯(0)催化的溴酚与(1,n)-二炔的脱芳香环化反应已经开发出来,用于构建两种新型的包含季碳中心的三环结构。该方法使用廉价的溴酚和易于连接的二炔。它具有广泛的底物范围,并能耐受各种官能团。商业上可获得的手性配体的初步结果表明对映选择性变体对于两种环化过程都是可行的。

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