Abstract
We report a method that enables the fast incorporation of carbon isotopes into the ipso carbon of phenols. Our approach relies on the synthesis of a 1,5-dibromo-1,4-pentadiene precursor, which upon lithium-halogen exchange followed by treatment with carbonate esters results in a formal [5 + 1] cyclization to form the phenol product. Using this strategy, we have prepared 12 1-13C-labeled phenols, show proof-of-concept for the labeling of phenols with carbon-14, and demonstrate phenol synthesis directly from cyclotron-produced [11C]CO2
Cite
CITATION STYLE
Lynch, C. F., Downey, J. W., Zhang, Y., Hooker, J. M., & Levin, M. D. (2023). Core-Labeling (Radio) Synthesis of Phenols. Organic Letters, 25(39), 7230–7235. https://doi.org/10.1021/acs.orglett.3c02838
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.