4.7 Article

[18F]Fluorination of o-carborane via nucleophilic substitution: towards a versatile platform for the preparation of 18F-labelled BNCT drug candidates

Journal

CHEMICAL COMMUNICATIONS
Volume 49, Issue 98, Pages 11491-11493

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc46695g

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Funding

  1. Ministerio de Ciencia e Innovacion [CTQ2009-08810]

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The mono-[F-18] fluorination of o-carborane via nucleophilic substitution is reported. The new radiochemical transformation uses cyclotron produced [F-18]F- and a carboranyl iodonium salt. Further derivatization of the F-18-labelled carborane is achieved by formation of the C-c-lithio salt and reaction with an aldehyde.

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