Rapid and Mild Syntheses of Radioiodine-Labeled Radiopharmaceuticals

Radioiodine-labeled pharmaceuticals have been used extensively in diagnostic nuclear medicine. We have developed a rapid and mild method for incorporating radioiodine into functionally substituted molecules. The new process involves the reaction of the radioiodide ion with organoboranes in the prese...

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Veröffentlicht in:The Journal of nuclear medicine (1978) 1981-10, Vol.22 (10), p.908-912
Hauptverfasser: Kabalka, George W, Gooch, E. Eugene, Sastry, Kunda A. R
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container_title The Journal of nuclear medicine (1978)
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creator Kabalka, George W
Gooch, E. Eugene
Sastry, Kunda A. R
description Radioiodine-labeled pharmaceuticals have been used extensively in diagnostic nuclear medicine. We have developed a rapid and mild method for incorporating radioiodine into functionally substituted molecules. The new process involves the reaction of the radioiodide ion with organoboranes in the presence of gentle oxidizing reagents. The radioiodide is utilized nearly quantitatively in a matter of seconds. The radiochemical yields are excellent, and parallel those obtained when iodine monochloride is reacted with organoboranes.
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source MEDLINE; EZB Electronic Journals Library
subjects Animals
Boranes - chemical synthesis
Boranes - metabolism
Chemical Phenomena
Chemistry
Female
Iodine Radioisotopes
Rats
Rats, Inbred Strains
Tissue Distribution
title Rapid and Mild Syntheses of Radioiodine-Labeled Radiopharmaceuticals
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