18F-trifluoromethylation of unmodified peptides with 5-18F-(trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate

The 18F-labeling of 5-(trifluoromethyl)-dibenzothiophenium trifluoromethanesulfonate, commonly referred to as the Umemoto reagent, has been accomplished applying a halogen exchange 18F-fluorination with 18F-fluoride, followed by oxidative cyclization with Oxone and trifluoromethanesulfonic anhydride...

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Κύριοι συγγραφείς: Verhoog, S, Kee, C, Wang, Y, Khotavivattana, T, Wilson, T, Kersemans, V, Smart, S, Tredwell, M, Davis, B, Gouverneur, V
Μορφή: Journal article
Γλώσσα:English
Έκδοση: American Chemical Society 2018
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author Verhoog, S
Kee, C
Wang, Y
Khotavivattana, T
Wilson, T
Kersemans, V
Smart, S
Tredwell, M
Davis, B
Gouverneur, V
author_facet Verhoog, S
Kee, C
Wang, Y
Khotavivattana, T
Wilson, T
Kersemans, V
Smart, S
Tredwell, M
Davis, B
Gouverneur, V
author_sort Verhoog, S
collection OXFORD
description The 18F-labeling of 5-(trifluoromethyl)-dibenzothiophenium trifluoromethanesulfonate, commonly referred to as the Umemoto reagent, has been accomplished applying a halogen exchange 18F-fluorination with 18F-fluoride, followed by oxidative cyclization with Oxone and trifluoromethanesulfonic anhydride. This new 18F-reagent allows for the direct chemoselective 18F-labeling of unmodified peptides at the thiol cysteine residue.
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institution University of Oxford
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publisher American Chemical Society
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spelling oxford-uuid:cce0b7b2-555b-4638-9ab8-35d91d03104d2022-03-27T07:24:56Z18F-trifluoromethylation of unmodified peptides with 5-18F-(trifluoromethyl)dibenzothiophenium trifluoromethanesulfonateJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:cce0b7b2-555b-4638-9ab8-35d91d03104dEnglishSymplectic Elements at OxfordAmerican Chemical Society2018Verhoog, SKee, CWang, YKhotavivattana, TWilson, TKersemans, VSmart, STredwell, MDavis, BGouverneur, VThe 18F-labeling of 5-(trifluoromethyl)-dibenzothiophenium trifluoromethanesulfonate, commonly referred to as the Umemoto reagent, has been accomplished applying a halogen exchange 18F-fluorination with 18F-fluoride, followed by oxidative cyclization with Oxone and trifluoromethanesulfonic anhydride. This new 18F-reagent allows for the direct chemoselective 18F-labeling of unmodified peptides at the thiol cysteine residue.
spellingShingle Verhoog, S
Kee, C
Wang, Y
Khotavivattana, T
Wilson, T
Kersemans, V
Smart, S
Tredwell, M
Davis, B
Gouverneur, V
18F-trifluoromethylation of unmodified peptides with 5-18F-(trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate
title 18F-trifluoromethylation of unmodified peptides with 5-18F-(trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate
title_full 18F-trifluoromethylation of unmodified peptides with 5-18F-(trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate
title_fullStr 18F-trifluoromethylation of unmodified peptides with 5-18F-(trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate
title_full_unstemmed 18F-trifluoromethylation of unmodified peptides with 5-18F-(trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate
title_short 18F-trifluoromethylation of unmodified peptides with 5-18F-(trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate
title_sort 18f trifluoromethylation of unmodified peptides with 5 18f trifluoromethyl dibenzothiophenium trifluoromethanesulfonate
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