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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Enantioselective aza-Diels-Alder reaction of Brassard's diene with aldimines catalyzed by chiral N,N'-dioxide-Yb(OTf)3 complex
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Enantioselective aza-Diels-Alder reaction of Brassard's diene with aldimines catalyzed by chiral N,N'-dioxide-Yb(OTf)3 complex

机译:N,N'-二氧化物-Yb(OTf)3配合物催化布拉萨德二烯与醛亚胺的对映选择性氮杂-Diels-Alder反应

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摘要

The chiral N,N'-dioxide-Yb(OTf)3 complex-catalyzed enantioselective aza-Diels-Alder reaction of Brassard's diene with aldimines has been developed, giving the corresponding α,β-unsaturated 8-lactam derivatives in moderate yields with good enantioselectivities (up to 81% ee and up to 99% ee by single recrystallization) under mild conditions. Isolation of the reaction intermediate indicates that this asymmetric aza-Diels-Alder reaction proceeds through a stepwise Mannich-type pathway.
机译:已开发了Brassard's二烯与醛亚胺的手性N,N'-二氧化物-Yb(OTf)3络合物催化的对映选择性aza-Diels-Alder反应,得​​到中等产率的相应α,β-不饱和8-内酰胺衍生物在温和条件下的对映选择性(高达81%ee,单重结晶高达99%ee)。分离反应中间体表明该不对称的氮杂-Diels-Alder反应通过逐步的曼尼希型途径进行。

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