Optimizing electrophilic 6-[18F]fluoro-L-DOPA synthesis utilizing low precursor concentration

被引:0
|
作者
Arora, G. [1 ]
Shukla, J. [1 ]
Gupta, P. [1 ]
Bandopadhyaya, G. [1 ]
机构
[1] All India Inst Med Sci, Delhi, India
关键词
D O I
暂无
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
引用
收藏
页码:S493 / S493
页数:1
相关论文
共 50 条
  • [1] Alternative solvents for electrophilic synthesis of 6-[18F]fluoro-L-DOPA
    Forsback, Sarita
    Eskola, Olli
    Bergman, Joergen
    Haaparanta, Merja
    Solin, Olof
    JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 2009, 52 (7-8): : 286 - 288
  • [2] Robotic synthesis of 6-[18F]fluoro-L-dopa
    Chang, CW
    Wang, HE
    Lin, HM
    Chtsai, CS
    Chen, JB
    Liu, RS
    NUCLEAR MEDICINE COMMUNICATIONS, 2000, 21 (09) : 799 - 802
  • [3] Advances in the automated synthesis of 6-[18F]Fluoro-L-DOPA
    Ângela C. B. Neves
    Ivanna Hrynchak
    Inês Fonseca
    Vítor H. P. Alves
    Mariette M. Pereira
    Amílcar Falcão
    Antero J. Abrunhosa
    EJNMMI Radiopharmacy and Chemistry, 6
  • [5] New approach to the nucleophilic synthesis of 6-[18F]fluoro-L-DOPA
    Wagner, F. M.
    Ermert, J.
    Coenen, H. H.
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2008, 35 : S162 - S163
  • [6] 6-[18F]Fluoro-L-DOPA by Radiofluorodestannylation: A Short and Simple Synthesis of a New Labelling Precursor
    Dolle, F.
    Demphel, S.
    Hinnen, F.
    Fournier, D.
    Journal of Labelled Compounds and Radiopharmaceuticals, 41 (02):
  • [7] 6-[18F]Fluoro-L-DOPA by radiofluorodestannylation : A short and simple synthesis of a new labelling precursor
    Serv. Hosp. Frederic Joliot, Dept. de Recherche Médicale, CEA, 4 Pl. du General Leclerc, F-91406 Orsay, France
    J. Label. Compd. Radiopharm., 2 (105-114):
  • [8] 6-[18F]fluoro-L-DOPA by radiofluorodestannylation:: A short and simple synthesis of a new labelling precursor
    Dolle, F
    Demphel, S
    Hinnen, F
    Fournier, D
    Vaufrey, F
    Crouzel, C
    JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 1998, 41 (02): : 105 - 114
  • [9] Electrophilic synthesis of 6-[18F]fluoro-L-DOPA using post-target produced [18F]F2
    Forsback, S.
    Eskola, O.
    Haaparanta, M.
    Bergman, J.
    Solin, O.
    RADIOCHIMICA ACTA, 2008, 96 (12) : 845 - 848
  • [10] Trifluoromethanesulfonic acid, an alternative solvent medium for the direct electrophilic fluorination of DOPA:: new syntheses of 6-[18F]fluoro-L-DOPA and 6-[18F]fluoro-D-DOPA
    Azad, Babak Behnam
    Chirakal, Raman
    Schrobilgen, Gary J.
    JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 2007, 50 (13-14): : 1236 - 1242