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- W2950489957 abstract "A facile, efficient and environmentally friendly methodology for the preparation of phenolic esters is realized via metal‐free coupling of carboxylic acids and arylboronic acids. This sequential one pot reaction, employing methyl propiolate as an activating reagent, proceeds through the formation of enol ester intermediate, followed by a nucleophilic attack on the C‐O bond under the oxidation of hydrogen peroxide. These studies display that enol esters, despite previously being overlooked as synthetic intermediates, would be the valuable building blocks for developing carbon–carbon and carbon–heteroatom bond‐forming reactions." @default.
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- W2950489957 date "2019-06-19" @default.
- W2950489957 modified "2023-09-27" @default.
- W2950489957 title "Enol Ester Intermediate Induced Metal-Free Oxidative Coupling of Carboxylic Acids and Arylboronic Acids" @default.
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- W2950489957 doi "https://doi.org/10.1002/ejoc.201900137" @default.
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