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首页> 外文期刊>The Journal of Organic Chemistry >Silver-Catalyzed Enantioselective Mannich Reaction of Diazoacetate Esters with N-Boc Aldimines
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Silver-Catalyzed Enantioselective Mannich Reaction of Diazoacetate Esters with N-Boc Aldimines

机译:用N-BOC醛氨对二氮杂乙酸酯酯的银催化的映选择性曼尼奇反应

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摘要

The highly enantioselective Mannich reaction of diazoacetate esters with N-Boc aldimines catalyzed by silver(I) triflate in the presence of (R)-DM-SEGPHOS is reported. The reaction is broad in scope with respect to the (hetero)aromatic aldehyde-derived aldimine and tolerates significant variability of the diazoacetate ester component. Yields and enantioselectivities are good to excellent, and the reaction can be performed on a gram scale with catalyst loadings as low as 1 mol %.
机译:报道,在(R)-DM-SEGPHOS存在下,用银(I)催化的N-BOC醛胺与N-BOC醛亚胺的高辅助选择性曼尼希反应。 该反应范围相对于(杂)芳族醛衍生的醛亚胺宽,并耐受二氮酸酯组分的显着变化。 产率和对映选择性好于优异,并且可以在克兰垢与催化剂载量低至1摩尔%的克兰垢进行反应。

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