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首页> 外文期刊>Organic letters >Asymmetric Catalytic Conjugate Addition of Acetaldehyde to Nitrodienynes/Nitroenynes: Applications to the Syntheses of (+)-α- Lycorane and Chiral β?Alkynyl Acids
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Asymmetric Catalytic Conjugate Addition of Acetaldehyde to Nitrodienynes/Nitroenynes: Applications to the Syntheses of (+)-α- Lycorane and Chiral β?Alkynyl Acids

机译:乙二醛/硝基乙炔的不对称催化共轭加成反应:在(+)-α-番红烷和手性β?炔酸合成中的应用

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摘要

The catalytic enantioselective conjugate addition of acetaldehyde to polyconjugated substrates, nitrodienynes and nitroenynes, has been accomplished using organocatalysis. Various functionalized 1,3-enynes and propargylic compounds were obtained in moderate to good yields with high enantioselectivity. The synthetic utilities of the conjugate addition reactions have been highlighted in the concise total synthesis of (+)-α-lycorane and the metal-free synthesis of chiral β-alkynyl acids.
机译:乙醛向多共轭底物硝基二炔和亚硝基炔的催化对映体选择性共轭加成反应已使用有机催化完成。以中等至良好的产率和高对映选择性获得了各种官能化的1,3-烯炔和炔丙基化合物。共轭加成反应的合成效用已在(+)-α-二十烷的简明全合成和手性β-炔酸的无金属合成中得到了强调。

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