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1,3-去氢-o-碳硼烷:生成与芳族化合物的反应。

1,3-Dehydro-o-carborane: generation and reaction with arenes.

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

Angew Chem Int Ed Engl. 2014 Aug 4;53(32):8488-91. doi: 10.1002/anie.201405023. Epub 2014 Jul 1.

Abstract

Like the importance of benzyne, witnessed in modern arene chemistry for decades, 1,2-dehydro-o-carborane (o-carboryne), a three-dimensional relative of benzyne, has been used as a synthon for generating a wide range of cage, carbon-functionalized carboranes over the past 20 years. However, the selective B functionalization of the cage still represents a challenging task. Disclosed herein is the first example of 1,3-dehydro-o-carborane featuring a cage C-B bond having multiple bonding characters, and is successfully generated by treatment of 3-diazonium-o-carborane tetrafluoroborate with non-nucleophilic bases. This presents a new methodology for simultaneous functionalization of both cage carbon and boron vertices.

摘要

类似于苯炔在现代芳环化学中几十年来的重要性,1,2-去氢-o-卡硼烷(o-卡宾),苯炔的三维类似物,在过去的 20 年中被用作生成广泛的笼状、碳官能化卡硼烷的前体。然而,笼的选择性 B 官能化仍然是一项具有挑战性的任务。本文首次报道了具有笼 C-B 键的 1,3-去氢-o-卡硼烷,其特征在于具有多种成键性质,并通过 3-重氮-o-卡硼烷四氟硼酸盐与非亲核碱的处理成功生成。这为同时对笼碳原子和硼顶点进行官能化提供了一种新的方法。

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