One-Step Annulative π-Extension of Alkynes with Dibenzosiloles or Dibenzogermoles by Palladium/o-chloranil Catalysis

被引:59
作者
Ozaki, Kyohei [1 ]
Murai, Keiichiro [1 ]
Matsuoka, Wataru [1 ]
Kawasumi, Katsuaki [1 ]
Ito, Hideto [1 ]
Itami, Kenichiro [1 ,2 ,3 ]
机构
[1] Nagoya Univ, Grad Sch Sci, Nagoya, Aichi 4648602, Japan
[2] Nagoya Univ, Inst Transformat Biomol WPI ITbM, Nagoya, Aichi 4648601, Japan
[3] Nagoya Univ, JST ERATO, Itami Mol Nanocarbon Project, Nagoya, Aichi 4648602, Japan
关键词
alkynes; dibenzosiloles; palladium; polycyclic aromatic hydrocarbons; pi-extension; POLYCYCLIC AROMATIC-HYDROCARBONS; C-C-BOND; GRAPHENE NANORIBBONS; ACTIVATION; BENZANNULATION; PHENANTHRENES; NANOGRAPHENE; BIPHENYLENE; DERIVATIVES; COMPLEXES;
D O I
10.1002/anie.201610374
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Reliable and short synthetic routes to polycyclic aromatic hydrocarbons and nanographenes are important in materials science. Herein, we report an efficient one-step annulative p-extension reaction of alkynes that provides access to diarylphenanthrenes and related nanographene precursors. In the presence of a cationic palladium/o-chloranil catalyst system and dibenzosiloles or dibenzogermoles as p-extending agents, a variety of diarylacetylenes are transformed successfully into 9,10-diarylphenanthrenes in a single step with good functional-group tolerance. Furthermore, double p-extension reactions of 1,4-bis(phenylethynyl) benzene and diphenyl-1,3-butadiyne are demonstrated, affording oligoarylene products, which show potential for application in the synthesis of larger polycyclic aromatic hydrocarbons and nanographenes.
引用
收藏
页码:1361 / 1364
页数:4
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