Scanning nitrogen in sp <sup>3</sup> -rich scaffolds enabled by carbonyl-to-nitrogen atom swap
-rich scaffolds enabled by the exchange of a carbonyl group with an amine moiety, formally achieving a carbonyl-to-nitrogen (CO-to-N) atom swap. Because ketone positional isomers can be readily obtained through carbonyl transposition or carbon-hydrogen oxidation from a common carbocyclic precursor, the CO-to-N atom swap greatly streamlines the preparation of SNH positional analogs and obviates the need for multiple de novo syntheses. The CO-to-N reaction exhibits exceptional functional group compatibility and generality, which makes it well suited for late-stage modification of complex bioactive molecules and for isotopic labeling.
Authors
- Zhehan Liang
- Z Zhang
- Rong Ye
- Guangbin Dong
Institutions
- University of Chicago (US)
Publication Details
- Journal
- Science
- Published
- 2026-04-30
- DOI
- https://doi.org/10.1126/science.aef0610
- Citations
- 1
- Primary Topic
- Chemical Reactions and Isotopes
- Type
- article
- Field-Weighted Citation Impact
- 13.75
Funders
- National Institute of General Medical Sciences