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
Title
Supporting Information
Description
Detailed experimental procedures, supplemental figures, and characterization data for all new compounds
Actions



![Author ORCID: We display the ORCID iD icon alongside authors names on our website to acknowledge that the ORCiD has been authenticated when entered by the user. To view the users ORCiD record click the icon. [opens in a new tab]](https://www.cambridge.org/engage/assets/public/coe/logo/orcid.png)