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Hf(OTf)4 as a Highly Potent Catalyst for the Synthesis of Mannich Bases under Solvent-Free Conditions

机译:Hf(OTf)4作为无溶剂条件下合成曼尼希碱的高效催化剂

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摘要

Hf(OTf) was identified as a highly potent catalyst (0.1–0.5 mol%) for three-component Mannich reaction under solvent-free conditions. Hf(OTf) -catalyzed Mannich reaction exhibited excellent regioselectivity and diastereoselectivity when alkyl ketones were employed as substrates. H NMR tracing of the H/D exchange reaction of ketones in MeOH- indicated that Hf(OTf) could significantly promote the keto-enol tautomerization, thereby contributing to the acceleration of reaction rate.
机译:Hf(OTf)被确定为无溶剂条件下三组分曼尼希反应的高效催化剂(0.1-0.5 mol%)。当使用烷基酮作为底物时,Hf(OTf)催化的曼尼希反应表现出极好的区域选择性和非对映选择性。酮在MeOH中的H / D交换反应的1 H NMR示踪表明,Hf(OTf)可以显着促进酮-烯醇互变异构,从而有助于加快反应速率。

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