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- W4376279269 endingPage "100010" @default.
- W4376279269 startingPage "100010" @default.
- W4376279269 abstract "The electrochemical oxidation of sec-alcohols has been achieved using MgBr2·6H2O as an inexpensive active bromine source and electrolyte under constant current conditions. The reactions smoothly proceed in a simple undivided cell, and aliphatic/benzylic sec-alcohols bearing heteroaromatics as well as aryl and alkyl groups are successfully converted to the corresponding ketones in good to excellent yields. In addition, the present reaction conditions selectively transform a secondary hydroxy moiety over different classes of hydroxy groups." @default.
- W4376279269 created "2023-05-13" @default.
- W4376279269 creator A5030032070 @default.
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- W4376279269 creator A5075184366 @default.
- W4376279269 creator A5077218081 @default.
- W4376279269 creator A5083301071 @default.
- W4376279269 date "2023-01-01" @default.
- W4376279269 modified "2023-10-14" @default.
- W4376279269 title "Electrochemical oxidation of sec-alcohols with MgBr2·6H2O" @default.
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- W4376279269 doi "https://doi.org/10.1016/j.tgchem.2023.100010" @default.
- W4376279269 hasPublicationYear "2023" @default.