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对映选择性合成和 S 型双氮杂薁的圆偏振发光增强。

Enantioselective synthesis and enhanced circularly polarized luminescence of S-shaped double azahelicenes.

机构信息

Department of Applied Chemistry, Graduate School of Engineering, Tokyo University of Agriculture and Technology , Koganei, Tokyo 184-8588, Japan.

出版信息

J Am Chem Soc. 2014 Apr 16;136(15):5555-8. doi: 10.1021/ja500841f. Epub 2014 Apr 4.

Abstract

The enantioselective synthesis of azahelicenes and S-shaped double azahelicenes has been achieved via the Au-catalyzed sequential intramolecular hydroarylation of alkynes. The use of excess AgOTf toward a Au(I) complex is crucial for this transformation. Interestingly, the circularly polarized luminescence activity of the S-shaped double azahelicenes was significantly higher than that of the azahelicenes.

摘要

通过金催化的炔烃顺序分子内氢芳化反应,实现了氮杂薁和 S 型双氮杂薁的对映选择性合成。该转化中使用过量的 AgOTf 对于 Au(I) 配合物至关重要。有趣的是,S 型双氮杂薁的圆偏振发光活性明显高于氮杂薁。

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