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One-carbon homologation of arylboronic acids: a convenient approach to the synthesis of pinacol benzylboronates
Wu, Chaoqiang ; Wu, Guojiao ; Zhang, Yan ; Wang, Jianbo
刊名ORGANIC CHEMISTRY FRONTIERS
2016
关键词IRIDIUM-CATALYZED BORYLATION CROSS-COUPLING REACTIONS C-H BONDS BENZYL HALIDES ALKENYLBORONIC ACIDS ALKYLBORON COMPOUNDS ESTERS METAL ORGANOBORANES BIS(PINACOLATO)DIBORON
DOI10.1039/c6qo00141f
英文摘要A transition-metal-free method for the synthesis of benzylic boronate esters with arylboronic acids and trimethylsilyldiazomethane (TMSCHN2) has been developed. This transformation is a straightforward homologation of arylboronic acids, which represents a unique approach toward the preparation of pinacol benzylboronates. The reaction has a wide substrate scope and good functional-group tolerance, and it can be scaled up easily.; 973 Program [2012CB821600]; National Nature Science Foundation of China [21272010, 21332002]; SCI(E); ARTICLE; wangjb@pku.edu.cn; 7; 817-822; 3
语种英语
内容类型期刊论文
源URL[http://ir.pku.edu.cn/handle/20.500.11897/492441]  
专题化学与分子工程学院
推荐引用方式
GB/T 7714
Wu, Chaoqiang,Wu, Guojiao,Zhang, Yan,et al. One-carbon homologation of arylboronic acids: a convenient approach to the synthesis of pinacol benzylboronates[J]. ORGANIC CHEMISTRY FRONTIERS,2016.
APA Wu, Chaoqiang,Wu, Guojiao,Zhang, Yan,&Wang, Jianbo.(2016).One-carbon homologation of arylboronic acids: a convenient approach to the synthesis of pinacol benzylboronates.ORGANIC CHEMISTRY FRONTIERS.
MLA Wu, Chaoqiang,et al."One-carbon homologation of arylboronic acids: a convenient approach to the synthesis of pinacol benzylboronates".ORGANIC CHEMISTRY FRONTIERS (2016).
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