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Aerobic Direct Dioxygenation of Terminal/Internal Alkynes to α-Hydroxyketones by an Fe Porphyrin Catalyst
Chemistry - An Asian Journal ( IF 3.5 ) Pub Date : 2021-09-14 , DOI: 10.1002/asia.202101019 Kento Kimura 1 , Takuya Kurahashi 1 , Seijiro Matsubara 1
Chemistry - An Asian Journal ( IF 3.5 ) Pub Date : 2021-09-14 , DOI: 10.1002/asia.202101019 Kento Kimura 1 , Takuya Kurahashi 1 , Seijiro Matsubara 1
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The synthesis of α-hydroxyketones through the dioxygenation of alkynes is reported. The reaction is mediated by an Fe porphyrin complex and pinacolborane at room temperature under air as a green oxidant, furnishing α-hydroxyketones in up to 93% yields. The mild reaction conditions allow chemoselective oxidation with good functional group tolerance.
中文翻译:
Fe 卟啉催化剂将末端/内部炔烃有氧直接双氧化为 α-羟基酮
报道了通过炔烃的双氧合合成 α-羟基酮。该反应由铁卟啉配合物和频哪醇硼烷在室温下作为绿色氧化剂介导,以高达 93% 的产率提供 α-羟基酮。温和的反应条件允许具有良好官能团耐受性的化学选择性氧化。
更新日期:2021-11-17
中文翻译:
Fe 卟啉催化剂将末端/内部炔烃有氧直接双氧化为 α-羟基酮
报道了通过炔烃的双氧合合成 α-羟基酮。该反应由铁卟啉配合物和频哪醇硼烷在室温下作为绿色氧化剂介导,以高达 93% 的产率提供 α-羟基酮。温和的反应条件允许具有良好官能团耐受性的化学选择性氧化。