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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:衍生自二萘并环辛酸酯和亚磷酰胺配体的空气稳定的(π-烯丙基)铱络合物催化的高度区域选择性的烯丙基取代反应

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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:合成了衍生自二萘并环辛酸酯和亚磷酰胺配体的空气稳定的(π-烯丙基)铱络合物,发现该化合物在铱催化的烯丙基取代反应中非常有效。该催化剂具有优异的区域选择性和高稳定性。当使用NaCH(CO2Me)2作为亲核试剂时,烯丙基烷基化反应中的催化剂负载量可低至0.01 mol%。

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