Concerted nucleophilic aromatic substitution with 19F− and 18F−

Constanze N. Neumann, Jacob M. Hooker and Tobias Ritter ()
Additional contact information
Constanze N. Neumann: Harvard University
Jacob M. Hooker: Massachusetts General Hospital
Tobias Ritter: Harvard University

Nature, 2016, vol. 534, issue 7607, 369-373

Abstract: Nucleophilic aromatic substitution (SNAr) is the most commonly used method to generate arenes that contain 18F for use in PET imaging; here, an unusual concerted SNAr reaction is presented that is not limited to electron-poor arenes.

Date: 2016
References: Add references at CitEc
Citations: View citations in EconPapers (1)

Downloads: (external link)
https://www.nature.com/articles/nature17667 Abstract (text/html)
Access to the full text of the articles in this series is restricted.

Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.

Export reference: BibTeX RIS (EndNote, ProCite, RefMan) HTML/Text

Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:534:y:2016:i:7607:d:10.1038_nature17667

Ordering information: This journal article can be ordered from
https://www.nature.com/

DOI: 10.1038/nature17667

Access Statistics for this article

Nature is currently edited by Magdalena Skipper

More articles in Nature from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().