Crossref journal-article
Wiley
Chemistry – A European Journal (311)
Abstract

AbstractCarbon‐11 labeled isocyanates are efficiently prepared by dehydration of [11C]carbamate salts, which in turn are easily formed from cyclotron‐produced [11C]CO2 and amines in the presence of a CO2 fixation agent. The [11C]isocyanates are useful radiosynthons for the synthesis of a variety of [carbonyl‐11C]‐labeled asymmetrical ureas and carbamate esters. The method is well suited to incorporate any isotope of carbon, and is especially useful for positron emission tomography (PET) radiotracers for in vivo imaging. This is demonstrated by using the method to make [carbonyl‐11C]‐6‐hydroxy‐[1,1′‐biphenyl]‐3‐yl cyclohexylcarbamate which is a novel radiotracer for PET imaging of fatty acid amide hydrolase.

Bibliography

Wilson, A. A., Garcia, A., Houle, S., Sadovski, O., & Vasdev, N. (2010). Synthesis and Application of Isocyanates Radiolabeled with Carbon‐11. Chemistry – A European Journal, 17(1), 259–264. Portico.

Authors 5
  1. Alan A. Wilson (first)
  2. Armando Garcia (additional)
  3. Sylvain Houle (additional)
  4. Oleg Sadovski (additional)
  5. Neil Vasdev (additional)
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Dates
Type When
Created 14 years, 9 months ago (Nov. 12, 2010, 9:30 a.m.)
Deposited 1 year, 10 months ago (Oct. 16, 2023, 8:44 a.m.)
Indexed 3 days, 12 hours ago (Aug. 21, 2025, 2:02 p.m.)
Issued 14 years, 9 months ago (Nov. 12, 2010)
Published 14 years, 9 months ago (Nov. 12, 2010)
Published Online 14 years, 9 months ago (Nov. 12, 2010)
Published Print 14 years, 7 months ago (Jan. 3, 2011)
Funders 0

None

@article{Wilson_2010, title={Synthesis and Application of Isocyanates Radiolabeled with Carbon‐11}, volume={17}, ISSN={1521-3765}, url={http://dx.doi.org/10.1002/chem.201002345}, DOI={10.1002/chem.201002345}, number={1}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Wilson, Alan A. and Garcia, Armando and Houle, Sylvain and Sadovski, Oleg and Vasdev, Neil}, year={2010}, month=nov, pages={259–264} }