New efficient nickel-catalyzed cross-coupling reaction between two Csp3 centers
New efficient nickel-catalyzed cross-coupling reaction between two Csp3 centers
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DOI:
10.1021/jo982317b
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发表时间:
1999-05-14
影响因子:
3.6
通讯作者:
Knochel, P
中科院分区:
文献类型:
--
作者:
Giovannini, R;Stüdemann, T;Knochel, P
The presence of a remote unsaturation (double bond, carbonyl group, cyano group) in an alkyl halide facilitates its cross-coupling reaction with various diorganozincs in the presence of Ni(acac)(2) (7.5-10 mol % in THF/NMP mixtures). These results were used to develop a new general cross-coupling reaction between functionalized diorganozincs and alkyl iodides using m- or p-trifluoromethylstyrene as a reaction promotor and Ni(acac)(2) as a catalyst (7.5-10 mol %; -35 degrees C, 5-10 h) leading to a broad range of polyfunctional cross-coupling products'.