2007
DOI: 10.1016/j.nucmedbio.2007.06.012
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18F fluoroethylations: different strategies for the rapid translation of 11C-methylated radiotracers

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Cited by 20 publications
(13 citation statements)
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“…An important step was the finding that by addition of alkali iodides, the yield of [ 18 F]fluoroethylation could be significantly increased 10 as well as the fact that the reactivity of [ 18 F]FETs could be further improved by introduction of strong electron-withdrawing substituents such as e.g. in 2-[ 18 19,20 Acknowledging that application of HPLC-purified [ 18 F]FETs had a significant impact on the labeling yield, chemical and radiochemical purity of the final radiotracer 13,44 has triggered the development of innovative automated methods for production and purification of [ 18 [28][29][30][31] and equally in the [ 18 F]fluoroethylation of other amino acids like methionine and tryptophan. 33,73,[104][105][106] In radiotracer building, the reaction with [ 18 F]FETs is indispensable as has been demonstrated for a multitude of Oand N-[ 18 F]fluoroethylations, the radiolabeling of thiols 106,107,109 and the formation of [ 18 F]fluoroethyl-carboxylic esters, [63][64][65][66]102 -amides 89 and -phosphorus esters.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…An important step was the finding that by addition of alkali iodides, the yield of [ 18 F]fluoroethylation could be significantly increased 10 as well as the fact that the reactivity of [ 18 F]FETs could be further improved by introduction of strong electron-withdrawing substituents such as e.g. in 2-[ 18 19,20 Acknowledging that application of HPLC-purified [ 18 F]FETs had a significant impact on the labeling yield, chemical and radiochemical purity of the final radiotracer 13,44 has triggered the development of innovative automated methods for production and purification of [ 18 [28][29][30][31] and equally in the [ 18 F]fluoroethylation of other amino acids like methionine and tryptophan. 33,73,[104][105][106] In radiotracer building, the reaction with [ 18 F]FETs is indispensable as has been demonstrated for a multitude of Oand N-[ 18 F]fluoroethylations, the radiolabeling of thiols 106,107,109 and the formation of [ 18 F]fluoroethyl-carboxylic esters, [63][64][65][66]102 -amides 89 and -phosphorus esters.…”
Section: Discussionmentioning
confidence: 99%
“…To circumvent the latter drawback, intermediate purification steps for [ 18 F]FETs have been developed comprising solid phase extraction (SPE) as well as HPLCbased procedures, partly remote-controlled, which as a consequence, afford the implementation of a two-pot radiolabeling procedure. 12,13 This review will summarize the role of [ 18 F]FETs as a labeling block in PET radiochemistry, its usage in the synthesis of radiopharmaceuticals with clinical relevance like [ 18…”
Section: Introductionmentioning
confidence: 99%
“…All scans were acquired in 3-D mode for 90 minutes (51 frames: 12×5 s, 6×10 s, 3×20 s, 6×30 s, 9×60 s, 15×300 s) and were reconstructed (iterative filtered back-projection algorithm) to final images comprising a spatial resolution of 4.36mm full-width at half-maximum 1 cm next to the center of the field of view (matrix 128×128, 35 slices). The radioligand [ carbonyl -11C]WAY-100635 was prepared according to previously published methods [58] at the Cyclotron Unit of the PET Center. Each PET scan was complemented with arterial blood samples for the quantification of [ carbonyl - 11 C]WAY-100635 that were automatically drawn for first 10 minutes (ALLOGG, Mariefred, Sweden) and manually at 2, 5, 6, 7, 8, 10, 20, 40 and 60 minute of the measurement.…”
Section: Methodsmentioning
confidence: 99%
“…Hence, having developed a series of fluoroethyl-esters over the last five years [24][25][26][27][28][29], it was obvious for us to develop [ 18 F]FE@SUPPY:2. …”
Section: Generalmentioning
confidence: 99%