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Palladium-catalyzed tandem allylic substitution/cyclization and cascade hydrosilylated reduction: the influence of reaction parameters and hydrosilanes on the stereoselectivity

机译:钯催化串联烯丙基取代/环化和级联氢化硅烷化还原:反应参数和氢化硅烷对立体选择性的影响

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To shed light on the influence of reaction parameters on palladium-catalyzed tandem allylic alkylation in the presence of Fei-Phos (a chiral trans -1,2-diaminocyclohexane-derived phosphine ligand), the effect of different phosphine ligands, inorganic or organic bases, Br?nsted acids, and other additives on the asymmetric palladium-catalysed alkylation of catechol with allylic diacetate was investigated. In this reaction, 2-vinyl-2,3-dihydro-benzo[1,4]dioxin products with promising enantioselectivity were achieved in good yields. In addition, a novel palladium-catalyzed three-component and one-pot allylic substitution/cyclization/reduction reaction assisted by methylphenylsilane was reported with good selectivity.
机译:为了阐明在Fei-Phos(手性反式-1,2-二氨基环己烷衍生的膦配体)存在下反应参数对钯催化的串联烯丙基烷基化的影响,不同膦配体,无机或有机碱的影响,布朗斯台德酸和其他添加剂对烯丙基二乙酸酯在不对称钯催化的邻苯二酚烷基化反应中的作用进行了研究。在该反应中,以良好的收率获得了具有希望的对映选择性的2-乙烯基-2,3-二氢-苯并[1,4]二恶英产物。另外,报道了一种新型的钯催化的三组分和甲基苯基硅烷辅助的单锅烯丙基取代/环化/还原反应。

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