Unusual structure and reactivity of a homoleptic "super-ate" complex of iron:: Implications for Grignard additions, cross-coupling reactions, and the Kharasch deconjugation

被引:137
作者
Fürstner, A [1 ]
Krause, H [1 ]
Lehmann, CW [1 ]
机构
[1] Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
关键词
ate complexes; cross-coupling; Grignard reaction; iron; single-electron transfer;
D O I
10.1002/anie.200502859
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The additional molecule of methyllithium present in [(Me 4Fe)(MeLi)][Li(OEt2)]2 (1), the first structurally characterized ate complex of FeII bearing only alkyl substituents without any further stabilizing ligands (see picture: Fe: magenta; Li: cyan; O: red; C and H: gray), is a particularly remarkable structural feature and contributes to the fascinating reactivity profile of 1 in the title reactions. (Chemical Equation Presented). © 2006 Wiley-VCH Verlag GmbH & Co. KGaA.
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页码:440 / 444
页数:5
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