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Catalytic asymmetric hydroxylative dearomatization of 2-naphthols: synthesis of lacinilene derivatives

机译:2-萘酚的催化不对称羟基脱芳香化作用:拉西尼衍生物的合成

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摘要

An enantioselective hydroxylative dearomatization of 2-naphthols with oxaziridines has been accomplished using a N,N′-dioxide–scandium(III) complex catalyst. Various substituted ortho-quinols could be obtained in high yields (up to 99%) and enantioselectivities (up to 95?:?5 er). This methodology could be applied in the synthesis of bioactive lacinilenes in a gram-scale reaction. Based on the experimental investigations and previous work, a possible catalytic model was proposed.
机译:使用 N N '-二氧化-(( III )络合物催化剂,完成了使用恶唑烷对2-萘酚进行对映体选择性羟基化脱芳香化反应。可以以高收率(高达99%)和对映选择性(高达95?:?5 er)获得各种取代的-喹诺醇。该方法可用于克级反应中的生物活性乳菌素的合成。基于实验研究和先前的工作,提出了一种可能的催化模型。

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