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Asymmetric Palladium-Catalyzed Intramolecular α-Arylation of Aldehydes

机译:不对称钯催化的醛内分子内α-芳基化

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摘要

The prevalence of chiral quaternary stereocenters in many natural products has attracted a growing interest in the development of methods for their construction with absolute stereocontrol. In recent years, the α-arylation of carbonyl compounds has received a great deal of attention. Despite substantial advances, the asymmetric metal-catalyzed α-arylation of carbonyl compounds remains a formidable challenge, and few examples have been described.To the best of our knowledge, no examples of asymmetric metal-catalyzed α-arylation of aldehydes have yet been reported. Herein, we present the first asymmetric metal-catalyzed α-arylation of aldehydes forming all-carbon-substituted asymmetric centers in high yields and enantioselectivities (Scheme 1).
机译:在许多天然产物中,手性四元立体中心的盛行引起了人们对开发具有绝对立体控制作用的手性四元立体中心的兴趣。近年来,羰基化合物的α-芳基化受到了广泛的关注。尽管取得了重大进展,羰基化合物的不对称金属催化的α-芳基化仍然是一个艰巨的挑战,很少有实例被描述。据我们所知,尚未报道醛的不对称金属催化的α-芳基化的实例。 。本文中,我们提出了醛的第一个不对称金属催化的α-芳基化反应,形成高收率和对映选择性的全碳取代的不对称中心(方案1)。

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