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Tandem Aldol Condensation – Platinacycle-Catalyzed Addition Reactions of Aldehydes Methyl Ketones and Arylboronic Acids

机译:串联醛醇缩合 - 醛糖催化的醛甲基酮和芳基硼酸的添加反应

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摘要

Tandem aldol condensation of aldehydes with methyl ketones followed by anionic four-electron donor-based (Type I) platinacycle-catalyzed addition reactions of arylboronic acids to form β-arylated ketones is described. Good to excellent yields of β-arylated ketones were obtained for the tandem reactions of aromatic/aliphatic aldehydes, methyl ketones and arylboronic acids, and moderate yields were observed for the tandem reaction with α, β-unsaturated aldehydes as the aldehyde source.
机译:描述了醛与甲基酮的串联醇醛缩合,然后是阴离子四电子供体基(I型)铂金环催化的芳基硼酸加成反应,形成β-芳基化酮。对于芳族/脂肪族醛,甲基酮和芳基硼酸的串联反应,获得的β-芳基化酮的收率良好至优异,对于以α,β-不饱和醛为醛源的串联反应,获得的收率中等。

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