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• W2625492040 startingPage "283" @default.
• W2625492040 abstract "Lighting the way to carbon borylation Boron substituents provide versatile reactivity, and their utility has been emerging in pharmaceutical contexts. Fawcett et al. show that visible light can induce replacement of carboxylic acid groups with boronate esters, which will ease their introduction into a wide variety of compounds. Once the acids are activated with phthalimide substituents, they can react with catecholborane dimers under illumination in amide solvents, with no need for catalysts or other additives. The reaction appears to proceed by radical chain propagation after photoinitiation. Science , this issue p. 283" @default.
• W2625492040 created "2017-06-23" @default.
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• W2625492040 date "2017-07-21" @default.
• W2625492040 modified "2023-10-15" @default.
• W2625492040 title "Photoinduced decarboxylative borylation of carboxylic acids" @default.
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• W2625492040 doi "https://doi.org/10.1126/science.aan3679" @default.
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