Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong (China).
Angew Chem Int Ed Engl. 2014 Aug 4;53(32):8488-91. doi: 10.1002/anie.201405023. Epub 2014 Jul 1.
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.
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。