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Chiral Bronsted Acid-Catalyzed Formal α-Vinylation of Ketones for the Enantioselective Construction of Quaternary Carbon Centre

机译:酮的手性抗正囊催化正式α-乙烯基化用于季碳中心的映选择性建设

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摘要

α-Vinyl ketones having an all carbon quaternary stereogenic centre at the α-position are important structural motif due to its prevalence in natural products and bioactive compounds. Therefore, the development of efficient methods for the construction of them is one of the important subjects in organic synthesis. Whereas the direct coupling of an enolate nucleophile with a vinyl electrophile by transition metal catalysis has particularly emerged as a potent strategy for the enantioselective construction of the α-vinyl ketones having all carbon quaternary stereogenic centre, the organocatalytic method has not been established.
机译:具有在α-位置的所有碳季型立体元素中心的α-乙烯基酮是重要的结构基质,因为它在天然产物和生物活性化合物中的流行率。因此,开发有效的构建方法是有机合成中的重要科目之一。然而,通过过渡金属催化与乙烯基亲电性的直接偶联含有乙烯基亲液的直接偶联特别出现为具有所有碳季型立体中心的α-乙烯基酮的对映选择性构建的有效策略,但尚未建立有机催化方法。

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