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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Highly regioselective allylic substitution reactions catalyzed by an air-stable (π-Allyl)iridium complex derived from dinaphthocyclooctatetraene and a phosphoramidite ligand
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Highly regioselective allylic substitution reactions catalyzed by an air-stable (π-Allyl)iridium complex derived from dinaphthocyclooctatetraene and a phosphoramidite ligand

机译:通过衍生自二甲萘CloocoCtattaene和亚磷酰胺配体的空气稳定(π-烯丙基)铱络合物催化的高度区域选择性烯丙基取代反应

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摘要

An air-stable (π-allyl)iridium complex derived from dinaphthocyclooctatetraene and a phosphoramidite ligand has been synthesized and found to be highly efficient in iridium-catalyzed allylic substitution reactions. This catalyst features excellent regioselectivity and high stability. When NaCH(CO2Me)2 was used as the nucleophile, the catalyst loading in allylic alkylation reactions can be as low as 0.01 mol%.
机译:已经合成了来自Dinaphthocycloococtettraene和磷酰胺酰亚胺配体的空气稳定(π-烯丙基)铱络合物,发现在铱催化的烯丙基替代反应中具有高效。 该催化剂具有优异的区域选择性和高稳定性。 当NACH(CO2ME)2用作亲核试剂时,烯丙基烷基化反应中的催化剂负载可以低至0.01mol%。

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