Hwang Chiwon, Lee Yeosan, Kim Minjae, Seo Younggyu, Cho Seung Hwan
Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
Institute for Convergence Research and Education in Advanced Technology (I-CREATE), Yonsei University, Seoul, 03722, Republic of Korea.
Angew Chem Int Ed Engl. 2022 Sep 12;61(37):e202209079. doi: 10.1002/anie.202209079. Epub 2022 Aug 1.
The development of new approaches to installing diverse carbon fragments to a nitrogen atom has attracted considerable attention in chemical science. While numerous strategies have been devised to forge C(sp )-N bonds, one conceptually powerful and straightforward approach is to insert a transformable sp -carbon unit onto a nitrogen atom for modular diversification. Here we describe the successful synthesis of halo-diborylmethanes and their applications to the preparation of nitrogen-substituted diborylmethanes through their homologative coupling with a variety of nitrogen nucleophiles including biologically relevant molecules. This process exhibits a remarkably broad substrate scope, and the usefulness of the obtained compounds is demonstrated by the modular diversification of the diborylmethyl group to access various nitrogen-containing molecules.
在化学科学领域,开发将各种碳片段连接到氮原子上的新方法已引起了相当大的关注。虽然已经设计出许多策略来形成C(sp )-N键,但一种概念上强大且直接的方法是将一个可转化的sp -碳单元插入到氮原子上,以实现模块化多样化。在此,我们描述了卤代二硼甲烷的成功合成及其通过与包括生物相关分子在内的各种氮亲核试剂进行同系偶联来制备氮取代二硼甲烷的应用。该过程展现出非常广泛的底物范围,并且通过二硼甲基基团的模块化多样化来获得各种含氮分子,证明了所得化合物的实用性。