Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Ulrike, Filp"'
Publikováno v:
European Journal of Organic Chemistry. 2017:5592-5596
The use of various quaternary ammonium salts as chiral phase-transfer catalysts allowed effective and stereoselective radiochemical [11C]alkylation to obtain functionalized dipeptides. We herein report a broadly applicable procedure for the asymmetri
Autor:
Ulrike Filp, Alex J. Poot, Carlotta Taddei, Albert D. Windhorst, Anna Pees, Aleksandra Pekošak, Antony D. Gee
Publikováno v:
European Journal of Organic Chemistry. 2017:5154-5162
Here we present a new Michael addition reaction utilizing carbon-11 labeled acrylic esters and amides. Subsequently, reactions of these synthons with commercially available Schiff base precursors are performed to produce [11C]glutamate and [11C]gluta
Publikováno v:
Pekošak, A, Filp, U, Poot, A J & Windhorst, A D 2018, ' From Carbon-11-Labeled Amino Acids to Peptides in Positron Emission Tomography : the Synthesis and Clinical Application ', Molecular Imaging and Biology, vol. 20, no. 4, pp. 510-532 . https://doi.org/10.1007/s11307-018-1163-5
Radiolabeled amino acids, their derivatives and peptides have a broad scope of application and can be used as receptor ligands, as well as enzyme substrates for many different diseases as radiopharmaceutical tracers. Over the past few decades, the ap
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 58:342-348
Positron emission tomography has increased the demand for new carbon-11 radiolabeled tracers and building blocks. A promising radiolabeling synthon is [11C]benzyl iodide ([11C]BnI), because the benzyl group is a widely present functionality in biolog
Autor:
Albert D. Windhorst, Uta Funke, Alex J. Poot, Aleksandra Pekošak, Ulrike Filp, Lonneke Rotteveel, Adriaan A. Lammertsma
Publikováno v:
Rotteveel, L, Poot, A J, Funke, U, Pekošak, A, Filp, U, Lammertsma, A A & Windhorst, A D 2017, ' Radiosynthesis of 1-iodo-2-[ 11 C]methylpropane and 2-methyl-1-[ 11 C]propanol and its application for alkylation reactions and C―C bond formation ', Journal of Labelled Compounds and Radiopharmaceuticals, vol. 60, no. 12, pp. 566-576 . https://doi.org/10.1002/jlcr.3536
Journal of Labelled Compounds and Radiopharmaceuticals, 60(12), 566-576. John Wiley and Sons Ltd
Journal of Labelled Compounds and Radiopharmaceuticals, 60(12), 566-576. John Wiley and Sons Ltd
The multitude of biologically active compounds requires the availability of a broad spectrum of radiolabeled synthons for the development of positron emission tomography (PET) tracers. The aim of this study was to synthesize 1-iodo-2-[11C]methylpropa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f54f37610dc09cbaedb9506ce32f93d
https://research.vumc.nl/en/publications/93800d09-bc91-46c9-9a09-e1978be8e18e
https://research.vumc.nl/en/publications/93800d09-bc91-46c9-9a09-e1978be8e18e
Autor:
Lonneke, Rotteveel, Alex J, Poot, Uta, Funke, Aleksandra, Pekošak, Ulrike, Filp, Adriaan A, Lammertsma, Albert D, Windhorst
Publikováno v:
Journal of labelled compoundsradiopharmaceuticals. 60(12)
The multitude of biologically active compounds requires the availability of a broad spectrum of radiolabeled synthons for the development of positron emission tomography (PET) tracers. The aim of this study was to synthesize 1-iodo-2-[
Publikováno v:
Organic and Biomolecular Chemistry, 15(3), 570-575. Royal Society of Chemistry
Pekošak, A, Filp, U, Škrinjar, J, Poot, A J & Windhorst, A D 2017, ' A rapid and highly enantioselective C-11 C bond formation of l-[ 11 C]phenylalanine via chiral phase-transfer catalysis ', Organic and Biomolecular Chemistry, vol. 15, no. 3, pp. 570-575 . https://doi.org/10.1039/c6ob02633h
Pekošak, A, Filp, U, Škrinjar, J, Poot, A J & Windhorst, A D 2017, ' A rapid and highly enantioselective C-11 C bond formation of l-[ 11 C]phenylalanine via chiral phase-transfer catalysis ', Organic and Biomolecular Chemistry, vol. 15, no. 3, pp. 570-575 . https://doi.org/10.1039/c6ob02633h
A rapid method for the synthesis of carbon-11 radiolabeled phenylalanine was developed using a chiral phase-transfer catalyst and a sub-nanomolar quantity of [11C]benzyl iodide as a radio-precursor. Based on a reported synthesis of [11C]benzyl iodide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::663a15621a39c5d124fee8e37f4cd78a
https://research.vumc.nl/en/publications/4e24e542-26f3-434b-80d9-ade94904bce6
https://research.vumc.nl/en/publications/4e24e542-26f3-434b-80d9-ade94904bce6
Publikováno v:
TETRAHEDRON, 72(41), 6551-6557. Elsevier Limited
Filp, U, Pekosak, A, Poot, A J & Windhorst, A D 2016, ' Enantioselective synthesis of carbon-11 labeled L-alanine using phase transfer catalysis of Schiff bases ', TETRAHEDRON, vol. 72, no. 41, pp. 6551-6557 . https://doi.org/10.1016/j.tet.2016.08.069
Filp, U, Pekosak, A, Poot, A J & Windhorst, A D 2016, ' Enantioselective synthesis of carbon-11 labeled L-alanine using phase transfer catalysis of Schiff bases ', TETRAHEDRON, vol. 72, no. 41, pp. 6551-6557 . https://doi.org/10.1016/j.tet.2016.08.069
Radiolabeled amino acids are an important class of compounds that can be used for Positron Emission Tomography (PET) imaging of the amino acid transporter status of various diseases e.g., cancer. Current radiochemistry techniques do not offer synthes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de09b2cf6bfada9ab9990adc472cd2b2
https://research.vumc.nl/en/publications/233647ed-bdcf-4c41-9c71-3778389a14b6
https://research.vumc.nl/en/publications/233647ed-bdcf-4c41-9c71-3778389a14b6
Publikováno v:
Journal of labelled compoundsradiopharmaceuticals. 58(8)
Positron emission tomography has increased the demand for new carbon-11 radiolabeled tracers and building blocks. A promising radiolabeling synthon is [(11) C]benzyl iodide ([(11) C]BnI), because the benzyl group is a widely present functionality in
Autor:
Radchenko, V.1, Engle, J.1, Roy, C.2, Griswold, J.2, Nortier, M.1, Birnbaum, E.1, Brugh, M.1, Mirzadeh, S.2, John, K.1, Fassbender, M.1, Zhai, Chuangyan3, Franssen, Gerben4, Petrik, Milos5, Laverman, Peter4, Decristoforo, Clemens3,6, Samia, Ait-Mohand7,8, Véronique, Dumulon-Perreault9,10, Brigitte, Guérin, Summer, D.3, Kroess, A.3
Publikováno v:
EJNMMI Radiopharmacy & Chemistry. Jun2016 Supplement, Vol. 1, p1-37. 37p.