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- W2570304792 abstract "A transition-metal-free and room-temperature coupling/decarboxylation reaction between α-oxocarboxylates and α-bromoketones is reported herein. It represents the first mild and regioselective synthesis of either 1,2- or 1,3-diketones from the same starting materials. Notably, the regioselectivity is simply controlled by solvents. The preliminary experimental data and DFT calculations suggest sequential Darzens-type coupling, alkaline hydrolysis, KOH-promoted oxirane opening and decarboxylation in one pot. This method is efficient for the synthesis of α,β-epoxy-γ-butyrolactone and curcuminoids." @default.
- W2570304792 created "2017-01-13" @default.
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- W2570304792 date "2017-01-18" @default.
- W2570304792 modified "2023-10-15" @default.
- W2570304792 title "Room-Temperature Coupling/Decarboxylation Reaction of α-Oxocarboxylates with α-Bromoketones: Solvent-Controlled Regioselectivity for 1,2- and 1,3-Diketones" @default.
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- W2570304792 doi "https://doi.org/10.1021/acs.joc.6b02575" @default.
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