[18F]Fluorination of o-carborane via nucleophilic substitution: towards a versatile platform for the preparation of 18F-labelled BNCT drug candidates
作者:Kiran B. Gona、Vanessa Gómez-Vallejo、Daniel Padro、Jordi Llop
DOI:10.1039/c3cc46695g
日期:——
The mono-[(18)F]fluorination of o-carborane via nucleophilicsubstitution is reported. The new radiochemical transformation uses cyclotron produced [(18)F]F(-) and a carboranyl iodonium salt. Further derivatization of the (18)F-labelled carborane is achieved by formation of the C(c)-lithio salt and reaction with an aldehyde.