双生的
对映选择合成
酮
反应性(心理学)
催化作用
化学
基质(水族馆)
有机化学
联苯
医学
海洋学
替代医学
病理
地质学
作者
Scott E. Denmark,Hayao Matsuhashi
摘要
Two structurally dissimilar, chiral fluoro ketones have been prepared and their potential as enantioselective catalysts for asymmetric epoxidation with Oxone has been evaluated. The tropinone-based ketone (−)-5 was easily prepared and showed excellent reactivity but only modest enantioselectivity. The biphenyl-based ketone (−)-6 was prepared in a somewhat lengthy synthesis (along with its monofluoro and geminal fluoro analogues). This ketone exhibited only modest reactivity; 30 mol % of (−)-6 was needed to bring about complete conversion in a reasonable time. The enantioselectivity of this catalyst was generally much higher, but again very substrate dependent.
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