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Recent Advances of S–(18)F Radiochemistry for Positron Emission Tomography

[Image: see text] The click chemistry of sulfur(VI) fluoride exchange (SuFEx) has facilitated the widespread application of sulfur–fluoride compounds such as sulfonyl fluorides, fluorosulfates, and sulfamoyl fluorides in various fields, especially in the development of (18)F ligands for PET (positro...

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Autores principales: Deng, Xiaoyun, Zhu, Xiaohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586020/
https://www.ncbi.nlm.nih.gov/pubmed/37867643
http://dx.doi.org/10.1021/acsomega.3c05594
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author Deng, Xiaoyun
Zhu, Xiaohua
author_facet Deng, Xiaoyun
Zhu, Xiaohua
author_sort Deng, Xiaoyun
collection PubMed
description [Image: see text] The click chemistry of sulfur(VI) fluoride exchange (SuFEx) has facilitated the widespread application of sulfur–fluoride compounds such as sulfonyl fluorides, fluorosulfates, and sulfamoyl fluorides in various fields, especially in the development of (18)F ligands for PET (positron emission tomography) imaging. In recent years, the prominent progress of sulfur–[(18)F]fluoride compounds has been achieved through the combination of (18)F and sulfur–fluoride chemistry. These compounds serve as potential (18)F tracers, (18)F synthons, and reagents for (18)F-fluorination, thereby complementing the range of (18)F ligands, typically C–(18)F structures, used in PET studies. This review aims to provide an overview of S–(18)F labeling reactions through examples of relevant (18)F compounds and highlight the advancements and breakthroughs achieved in the past decade.
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spelling pubmed-105860202023-10-20 Recent Advances of S–(18)F Radiochemistry for Positron Emission Tomography Deng, Xiaoyun Zhu, Xiaohua ACS Omega [Image: see text] The click chemistry of sulfur(VI) fluoride exchange (SuFEx) has facilitated the widespread application of sulfur–fluoride compounds such as sulfonyl fluorides, fluorosulfates, and sulfamoyl fluorides in various fields, especially in the development of (18)F ligands for PET (positron emission tomography) imaging. In recent years, the prominent progress of sulfur–[(18)F]fluoride compounds has been achieved through the combination of (18)F and sulfur–fluoride chemistry. These compounds serve as potential (18)F tracers, (18)F synthons, and reagents for (18)F-fluorination, thereby complementing the range of (18)F ligands, typically C–(18)F structures, used in PET studies. This review aims to provide an overview of S–(18)F labeling reactions through examples of relevant (18)F compounds and highlight the advancements and breakthroughs achieved in the past decade. American Chemical Society 2023-10-02 /pmc/articles/PMC10586020/ /pubmed/37867643 http://dx.doi.org/10.1021/acsomega.3c05594 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Deng, Xiaoyun
Zhu, Xiaohua
Recent Advances of S–(18)F Radiochemistry for Positron Emission Tomography
title Recent Advances of S–(18)F Radiochemistry for Positron Emission Tomography
title_full Recent Advances of S–(18)F Radiochemistry for Positron Emission Tomography
title_fullStr Recent Advances of S–(18)F Radiochemistry for Positron Emission Tomography
title_full_unstemmed Recent Advances of S–(18)F Radiochemistry for Positron Emission Tomography
title_short Recent Advances of S–(18)F Radiochemistry for Positron Emission Tomography
title_sort recent advances of s–(18)f radiochemistry for positron emission tomography
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586020/
https://www.ncbi.nlm.nih.gov/pubmed/37867643
http://dx.doi.org/10.1021/acsomega.3c05594
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