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通过亲电芳香硼化反应合成吡啶硼烷配合物。

Synthesis of pyridine-borane complexes via electrophilic aromatic borylation.

机构信息

Department of Synthetic Chemistry and Biological Chemistry, Kyoto University, Katsura, Kyoto 615-8510, Japan.

出版信息

J Org Chem. 2010 Dec 17;75(24):8709-12. doi: 10.1021/jo101920p. Epub 2010 Nov 23.

DOI:10.1021/jo101920p
PMID:21090764
Abstract

Pyridine-borane complexes were synthesized from 2-arylpyridines through an electrophilic aromatic borylation reaction with BBr(3). The intermediate 2-(2-dibromoborylaryl)pyridines were stable enough to be handled in air and served as the synthetic platform for variously substituted pyridine-borane complexes. This facile method would be useful for the synthesis of aza-π-conjugated materials having boron-nitrogen coordination.

摘要

通过三溴化硼(BBr(3))的亲电芳香硼酸化反应,从 2-芳基吡啶合成了吡啶硼烷配合物。中间体 2-(2-二溴硼基芳基)吡啶足够稳定,可以在空气中处理,并且可用作各种取代的吡啶硼烷配合物的合成平台。这种简便的方法将有助于合成具有硼-氮配位的氮杂-π 共轭材料。

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