Construction\nof Lactones via Ligand-Enabled Ni-Catalyzed\nAlkene Hydroxylarylation/Lactonization

Here, we report the preparation of\nlactones via Ni-catalyzed alkene\nhydroxylarylation and sequential intramolecular lactonization with\nO<sub>2</sub> as a green oxidant and oxygen source. The bulky 1,3-diketone\nligand is crucial by enabling Ni-catalyzed hydroxylarylation of alkenes,\nproviding numerous phthalide and furanone derivatives with high efficiency\nunder mild conditions. The synthetic value of this methodology was\nfurther demonstrated by the efficient synthesis of typhaphthalide\nand a monoamine oxidase B inhibitor.

Publication Details

Journal
Figshare
Published
2024-09-19
DOI
https://doi.org/10.1021/acs.orglett.4c03108.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
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article

Construction\nof Lactones via Ligand-Enabled Ni-Catalyzed\nAlkene Hydroxylarylation/Lactonization

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Mycorrhizal Fungi and Plant Interactions
article

Construction\nof Lactones via Ligand-Enabled Ni-Catalyzed\nAlkene Hydroxylarylation/Lactonization

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Abstract

Here, we report the preparation of\nlactones via Ni-catalyzed alkene\nhydroxylarylation and sequential intramolecular lactonization with\nO<sub>2</sub> as a green oxidant and oxygen source. The bulky 1,3-diketone\nligand is crucial by enabling Ni-catalyzed hydroxylarylation of alkenes,\nproviding numerous phthalide and furanone derivatives with high efficiency\nunder mild conditions. The synthetic value of this methodology was\nfurther demonstrated by the efficient synthesis of typhaphthalide\nand a monoamine oxidase B inhibitor.

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Mycorrhizal Fungi and Plant Interactions
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Construction\nof Lactones via Ligand-Enabled Ni-Catalyzed\nAlkene Hydroxylarylation/Lactonization · Figshare (2024) | TGRS Research Map | TGRS