Automated radiochemical synthesis of pharmaceutical grade [18F]FLT using 3-N-Boc-5’-O-dimethoxytrityl-3′-O-nosyl-thymidine precursor and its Sep-Pak® purification employing selective elution from reversed phase

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dc.contributor.authorMitra, A.
dc.contributor.authorChakraborty, A.
dc.contributor.authorUpadhye, T.
dc.contributor.authorTawate, M.
dc.contributor.authorLad, S.
dc.contributor.authorSahu, S.
dc.contributor.authorRajesh, C.
dc.contributor.authorBagul, S.
dc.contributor.authorPawar, Y.
dc.contributor.authorRay, M. K.
dc.date.accessioned2024-11-11T09:20:05Z
dc.date.available2024-11-11T09:20:05Z
dc.date.issued2022
dc.description.divisionRMCen
dc.format.extent5020 bytes
dc.format.mimetypetext/html
dc.identifier.sourceJournal of Labelled Compounds and Radiopharmaceuticals, 2022. Vol. 65: pp. 206-222en
dc.identifier.urihttp://hdl.handle.net/123456789/27663
dc.language.isoenen
dc.subject[18F]fluorothymidineen
dc.subjectpreclinical study-PET/CTen
dc.subjectpurificationen
dc.subjectSep-Pak®en
dc.subject3-N-Boc-5'-O-dimethoxytrityl-3'-O-nosyl-thymidine precursoren
dc.titleAutomated radiochemical synthesis of pharmaceutical grade [18F]FLT using 3-N-Boc-5’-O-dimethoxytrityl-3′-O-nosyl-thymidine precursor and its Sep-Pak® purification employing selective elution from reversed phaseen
dc.typeArticleen

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