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.
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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) |
@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} }