Regioselective synthesis of carbon- and silicon-bridged 2-(N,N-Dialkylamino)ethyl-substituted cyclopentadienes

被引:0
|
作者
Müller, C [1 ]
Jutzi, P [1 ]
机构
[1] Univ Bielefeld, Fak Chem, D-33615 Bielefeld, Germany
来源
SYNTHESIS-STUTTGART | 2000年 / 03期
关键词
amino-functionalized cyclopentadienes; ansa-metallocenes; fulvenes; regioselectivity;
D O I
暂无
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[2-(N,N-Dialkylamino)ethy]cyclopentadienes have been used for the synthesis of the novel amino-functionalized silicon- and carbon-bridged cyclopentadiene derivatives 3a-c, 7, 10 and 13a-c. The C-C and C-Si coupling reactions described here are regioselective leading exclusively to the formation of 1,3-disubstituted isomers, as proven by H-1 NMR spectroscopy. The bis-cyclopentadienes 3a-c, 7, 10 and 13a-c can be deprotonated to the corresponding dianionic species.
引用
收藏
页码:389 / 394
页数:6
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