Diborylmethyl Group as a Transformable Building Block for the Diversification of Nitrogen-Containing Molecules

被引:35
作者
Hwang, Chiwon [1 ]
Lee, Yeosan [1 ]
Kim, Minjae [1 ]
Seo, Younggyu [1 ]
Cho, Seung Hwan [1 ,2 ]
机构
[1] Pohang Univ Sci & Technol POSTECH, Dept Chem, Pohang 37673, South Korea
[2] Yonsei Univ, Inst Convergence Res & Educ Adv Technol I CREATE, Seoul 03722, South Korea
基金
新加坡国家研究基金会;
关键词
Boron; Diversification; Halo-Diborylmethane; Homologation; Nitrogen; ASYMMETRIC TRANSFER HYDROGENATION; ALPHA-AMINO-ACIDS; ORGANIC-SYNTHESIS; BORONIC ESTERS; HYDROAMINATION; ALKYLATION; REAGENTS; LIGANDS; BOND; 1,1-DIBORYLALKANES;
D O I
10.1002/anie.202209079
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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(3))-N bonds, one conceptually powerful and straightforward approach is to insert a transformable sp(3)-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.
引用
收藏
页数:7
相关论文
共 8 条