Selective Dimerization of Aryl-substituted Terminal Alkynes on Bis(indenyl)zirconocene Derivatives

被引:7
|
作者
Ren, Shenyong [1 ,2 ,3 ]
Seki, Takashi [4 ]
Necas, David [1 ,2 ,3 ]
Shimizu, Hiroyuki [5 ]
Nakajima, Kiyohiko [6 ]
Kanno, Ken-ichiro [1 ,2 ,3 ]
Song, Zhiying [1 ,2 ,3 ]
Takahashi, Tamotsu [1 ,2 ,3 ]
机构
[1] Hokkaido Univ, Catalysis Res Ctr, Kita Ku, Sapporo, Hokkaido 0010021, Japan
[2] Hokkaido Univ, Grad Sch Pharmaceut Sci, Kita Ku, Sapporo, Hokkaido 0600812, Japan
[3] Japan Sci & Technol Agcy JST, SORST, Chiyoda Ku, Tokyo 1020075, Japan
[4] JX Nippon Oil & Energy Corp, Naka Ku, Yokohama, Kanagawa 2310815, Japan
[5] Japan Polyethylene Corp, Kawasaki Ku, Kawasaki, Kanagawa 2100865, Japan
[6] Aichi Univ Educ, Dept Chem, Kariya, Aichi 4488542, Japan
关键词
INDENYL COMPLEXES; BENZENE-DERIVATIVES; COUPLING REACTIONS; RING-SLIPPAGE; CYCLOADDITION; ACETYLENES; REACTIVITY; CONVERSION; CHEMISTRY; ZIRCONACYCLOPENTADIENES;
D O I
10.1246/cl.2011.1443
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dimerization of aryl-substituted terminal alkynes on indenyl zirconium complexes occurred in a selective way. 1,4-Aryl-1,3-diene derivatives were formed exclusively after hydrolysis. It is in sharp contrast to the reaction on [Cp2Zr] complexes.
引用
收藏
页码:1443 / 1444
页数:2
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