Abstract
The [1,2]-Brook rearrangement stands as a potent technique for constructing complex molecules. In this study, we showcase its power in the dearomatization of aromatic N-heterocycles. Through a concise four-step process that integrates lithiation, nucleophilic addition, Brook rearrangement and dearomatization reaction, we demonstrate a versatile strategy for generat-ing diverse non-aromatic N-heterocycles with functional capabilities. Various acyl silanes, halo-pyridines, and quinolines have been explored within this context.
Supplementary materials
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Supporting Information
Description
Experimental procedures, characterization data, and NMR spectra for all novel compounds
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