Abstract
Quaternary carbon centers pose a significant challenge in chemical synthesis. Harnessing the underexplored reactivity of titanacyclobutane intermediates, a strategy to construct functionalized all-carbon quaternary centers from ketones is described. This methodology streamlines access to a wide variety of azaspiro[3.n]alkanes that have emerged as valuable three-dimensional inputs for drug discovery.
Supplementary materials
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Supporting Information
Description
Detailed experimental procedures, supplemental figures, and characterization data for all new compounds
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