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- W4236855902 endingPage "18881" @default.
- W4236855902 startingPage "18876" @default.
- W4236855902 abstract "While halogenation is of key importance in synthesis and radioimaging, the currently available repertoire is largely designed to introduce a single halogen per molecule. This report makes the selective introduction of several different halogens accessible. Showcased here is the privileged stability of nontoxic aryl germanes under harsh fluorination conditions (that allow selective fluorination in their presence), while displaying superior reactivity and functional-group tolerance in electrophilic iodinations and brominations, outcompeting silanes or boronic esters under rapid and additive-free conditions. Mechanistic experiments and computational studies suggest a concerted electrophilic aromatic substitution as the underlying mechanism." @default.
- W4236855902 created "2022-05-12" @default.
- W4236855902 creator A5047300640 @default.
- W4236855902 creator A5064017378 @default.
- W4236855902 creator A5085731021 @default.
- W4236855902 date "2020-08-20" @default.
- W4236855902 modified "2023-10-18" @default.
- W4236855902 title "Orthogonal Stability and Reactivity of Aryl Germanes Enables Rapid and Selective (Multi)Halogenations" @default.
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