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铱催化邻位碳硼烷笼状硼烯的区域选择性烯丙基化反应:通过直接笼状 B-H 活化。

Iridium catalyzed regioselective cage boron alkenylation of o-carboranes via direct cage B-H activation.

机构信息

Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The Chinese University of Hong Kong , Shatin, N. T., Hong Kong, China.

出版信息

J Am Chem Soc. 2014 Nov 5;136(44):15513-6. doi: 10.1021/ja509557j. Epub 2014 Oct 22.

Abstract

Iridium catalyzed alkyne hydroboration with o-carborane cage B-H has been achieved, leading to the formation of a series of 4-B-alkenylated-o-carborane derivatives in high yields with excellent regioselectivity via direct B-H bond activation. In this reaction the carboxy group is used as a traceless directing group, which is removed during a one-pot process. After the confirmation of a key intermediate, a possible mechanism is proposed, involving a tandem sequence of Ir-mediated B-H activation, alkyne insertion, protonation, and decarboxylation.

摘要

铱催化的炔烃与 o-笼型碳硼烷 B-H 的氢硼化反应已经实现,通过直接 B-H 键活化,以高产率和优异的区域选择性得到了一系列 4-B-烯基化-o-碳硼烷衍生物。在这个反应中,羧基被用作无痕迹导向基团,在一锅法过程中被去除。在确认了一个关键中间体后,提出了一个可能的机理,涉及 Ir 介导的 B-H 活化、炔烃插入、质子化和脱羧的串联序列。

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