Ring-Closing Synthesis of Dibenzothiophene Sulfonium Salts and Their Use as Leaving Groups for Aromatic 18F-Fluorination-Reference-Cited by-同舟云学术

Ring-Closing Synthesis of Dibenzothiophene Sulfonium Salts and Their Use as Leaving Groups for Aromatic 18F-Fluorination

Published:2018-08-22 Issue:35 Volume:140 Page:11125-11132
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Gendron Thibault¹²^ORCID,Sander Kerstin¹²^ORCID,Cybulska Klaudia²,Benhamou Laure¹²,Sin Pak Kwan Brian¹²,Khan Aqsa²,Wood Michael²,Porter Michael J.²^ORCID,Årstad Erik¹²^ORCID

Affiliation:

1. Institute of Nuclear Medicine, University College London, 235 Euston Road (T-5), London NW1 2BU, United Kingdom

2. Department of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ, United Kingdom

Funder

Engineering and Physical Sciences Research Council

FP7 Health

UCL Hospitals Charitable Foundation

Wellcome Trust

Leonard Wolfson Experimental Neurology Centre

UCLH/UCL Department of Health's NIHR Biomedical Research Centres funding scheme

UCL Business

CRUK & EPSRC Comprehensive Cancer Imaging Centre

Mallinckrodt

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

http://pubs.acs.org/doi/pdf/10.1021/jacs.8b06730

Reference42 articles.

1. 18F-Labeling of Arenes and Heteroarenes for Applications in Positron Emission Tomography

2. Small Prosthetic Groups in 18 F-Radiochemistry: Useful Auxiliaries for the Design of 18 F-PET Tracers

3. Hypervalent aryliodine compounds as precursors for radiofluorination

4. A General Copper-Mediated Nucleophilic18F Fluorination of Arenes

5. Enhanced copper-mediated 18F-fluorination of aryl boronic esters provides eight radiotracers for PET applications

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