Electrophilic Synthesis of 6-L-[18F]FDOPA with [18F]F2: a progress report on gas target of Cyclotron TR-Flex

被引：0
|
作者：
Kniess, Torsten [1 ]
Kreller, Martin [1 ]
Zessin, Joerg [1 ]
Kopka, Klaus [1 ]
机构：
[1] Helmholtz Zentrum Dresden Rossendorf, Dresden, Germany
来源：
NUCLEAR MEDICINE AND BIOLOGY | 2023年 / 126卷
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：
P-292
引用
收藏
页码：S267 / S267
页数：1
相关论文
共 50 条
  • [21] Automated synthesis of n.c.a. [18F]FDOPA via nucleophilic aromatic substitution with [18F]fluoride
    Shen, B.
    Ehrlichmann, W.
    Uebele, M.
    Machulla, H. -J.
    Reischl, G.
    APPLIED RADIATION AND ISOTOPES, 2009, 67 (09) : 1650 - 1653
  • [22] The Use of [18F]F2 in Anhydrous Hydrogenfluoride. Preparation of 5-[18F]Fluorocytosine and its Conversion to 5-[18F]Fluorouracil
    Oberdorfer, F.
    Haberkorn, U.
    Weber, K.
    Firnau, G.
    Journal of Labelled Compounds and Radiopharmaceuticals,
  • [23] Progress in the synthesis of paroxetine-[18F]
    Landvatter, SW
    Games, KT
    Dannals, RF
    SYNTHESIS AND APPLICATIONS OF ISOTOPICALLY LABELLED COMPOUNDS 1997, 1998, : 99 - 102
  • [24] Synthesis of 2′-deoxy-2′-[18F]fluoro-β-D-arabinofuranosyl nucleosides, [18F]FAU, [18F]FMAU, [18F]FBAU and [18F]FIAU, as potential PET agents for imaging cellular proliferation -: Synthesis of [18F]labeled FAU, FMAU, FBAU, FIAU
    Mangner, TJ
    Klecker, RW
    Anderson, L
    Shields, AF
    NUCLEAR MEDICINE AND BIOLOGY, 2003, 30 (03) : 215 - 224
  • [25] Modification of the automatic synthesis method for [18F]-FDOPA production
    Antuganov, Dmitrii
    Ryzhkova, Daria
    Zykova, Tatiana
    Vinal'ev, Andrey
    Antuganova, Yulia
    Samburov, Oleg
    Zykov, Mikhail
    JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 2017, 60 : S457 - S457
  • [26] Post-target produced [18F]F2 in the production of PET radiopharmaceuticals
    Forsback, Sarita
    Solin, Olof
    RADIOCHIMICA ACTA, 2015, 103 (03) : 219 - 226
  • [27] Synthesis and Evaluation of Three Structurally Related 18F-Labeled Orvinols of Different Intrinsic Activities: 6-O-[18F]Fluoroethyl-diprenorphine ([18F]FDPN), 6-O-[18F]Fluoroethyl-buprenorphine ([18F]FBPN), and 6-O-[18F]Fluoroethyl-phenethyl-orvinol ([18F]FPEO)
    Schoultz, Bent W.
    Hjornevik, Trine
    Reed, Brian J.
    Marton, Janos
    Coello, Christopher S.
    Willoch, Frode
    Henriksen, Gjermund
    JOURNAL OF MEDICINAL CHEMISTRY, 2014, 57 (12) : 5464 - 5469
  • [28] [18F]Fluorination of an arylboronic ester using [18F]selectfluor bis(triflate): application to 6-[18F]fluoro-L-DOPA
    Stenhagen, Ida S. R.
    Kirjavainen, Anna K.
    Forsback, Sarita J.
    Jorgensen, Charlotte G.
    Robins, Edward G.
    Luthra, Sajinder K.
    Solin, Olof
    Gouverneur, Veronique
    CHEMICAL COMMUNICATIONS, 2013, 49 (14) : 1386 - 1388
  • [29] The synthesis of [18F]fluoroarenes from the reaction of cyclotron-produced [18F]fluoride ion with diaryliodonium salts
    Shah, A
    Pike, VW
    Widdowson, DA
    JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1998, (13): : 2043 - 2046
  • [30] 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
12345