Deprotonative cadmation of functionalized aromatics
Copyright policy )Deprotonative cadmation of functionalized aromatics
This communication describes the deproto-metalation of a large range of aromatics including heterocycles using a newly developed lithium-cadmium base; the reaction proceeds at room temperature with an excellent chemoselectivity and efficiency, and proved to be regioselective in most cases.
Molecular Structure, Hydrocarbons, Halogenated, Temperature, Stereoisomerism, Lithium, [CHIM.ORGA] Chemical Sciences/Organic chemistry, Models, Chemical, Heterocyclic Compounds, Benzene Derivatives, Organometallic Compounds, Protons, Cadmium
Molecular Structure, Hydrocarbons, Halogenated, Temperature, Stereoisomerism, Lithium, [CHIM.ORGA] Chemical Sciences/Organic chemistry, Models, Chemical, Heterocyclic Compounds, Benzene Derivatives, Organometallic Compounds, Protons, Cadmium
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