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  1. AU="Johansson-Holm, Linus"
  2. AU=Silvester Nicole
  3. AU="Ahmed H. El-Ghorab"
  4. AU="Kaori Yamamoto"
  5. AU="Cernei C."
  6. AU="Faiz Alfaiz"
  7. AU="Fallon, Anne"
  8. AU="Ramos, Davi L."
  9. AU="Mancini, Valentina"
  10. AU="Lamothe, Valérie"
  11. AU=Powell-Jackson P R AU=Powell-Jackson P R
  12. AU="Neeltje A Kootstra"
  13. AU=Gloria e Silva Filipe AU=Gloria e Silva Filipe
  14. AU="Shuaijia Hao"
  15. AU=Heinrichs Stefan
  16. AU="Khosravan, Shahla"
  17. AU=Garcia-Carracedo Dario
  18. AU="Lannon, Margaret C"
  19. AU=Khan Inam Danish
  20. AU="Choza, Juliana"
  21. AU=Tronin Andrey Y.
  22. AU="Singh, Jyoti"
  23. AU=Charlier Philippe
  24. AU="Thiermann, Horst"
  25. AU="Gullo, Paride"
  26. AU="Lewis, Gayle"
  27. AU=Jain Harshwardhan AU=Jain Harshwardhan
  28. AU="Gaur, Aman"
  29. AU=Huynh Thu P.
  30. AU=Giebel Clarissa
  31. AU=Laskin Daniel M

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  1. Artikel ; Online: Synthesis of Elaborate Benzofuran-2-carboxamide Derivatives through a Combination of 8-Aminoquinoline Directed C-H Arylation and Transamidation Chemistry.

    Oschmann, Michael / Johansson Holm, Linus / Pourghasemi-Lati, Monireh / Verho, Oscar

    Molecules (Basel, Switzerland)

    2020  Band 25, Heft 2

    Abstract: Herein, we present a short and highly modular synthetic route that involves 8-aminoquinoline directed C-H arylation and transamidation chemistry, and which enables access to a wide range of elaborate benzofuran-2-carboxamides. For the directed C-H ... ...

    Abstract Herein, we present a short and highly modular synthetic route that involves 8-aminoquinoline directed C-H arylation and transamidation chemistry, and which enables access to a wide range of elaborate benzofuran-2-carboxamides. For the directed C-H arylation reactions, Pd catalysis was used to install a wide range of aryl and heteroaryl substituents at the C3 position of the benzofuran scaffold in high efficiency. Directing group cleavage and further diversification of the C3-arylated benzofuran products were then achieved in a single synthetic operation through the utilization of a one-pot, two-step transamidation procedure, which proceeded via the intermediate
    Mesh-Begriff(e) Amides/chemistry ; Aminoquinolines/chemistry ; Benzene Derivatives/chemistry ; Benzofurans/chemistry ; Catalysis ; Molecular Structure
    Chemische Substanzen Amides ; Aminoquinolines ; Benzene Derivatives ; Benzofurans ; benzofuran (LK6946W774) ; 8-aminoquinoline (U34EAV21TG)
    Sprache Englisch
    Erscheinungsdatum 2020-01-15
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article
    ZDB-ID 1413402-0
    ISSN 1420-3049 ; 1431-5165 ; 1420-3049
    ISSN (online) 1420-3049
    ISSN 1431-5165 ; 1420-3049
    DOI 10.3390/molecules25020361
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel: Base-catalysed ¹⁸F-labelling of trifluoromethyl ketones. Application to the synthesis of ¹⁸F-labelled neutrophil elastase inhibitors

    Meyer, Denise N. / Cortés González, Miguel A. / Jiang, Xingguo / Johansson-Holm, Linus / Pourghasemi Lati, Monireh / Elgland, Mathias / Nordeman, Patrik / Antoni, Gunnar / Szabó, Kálmán J.

    Chemical communications. 2021 Aug. 25, v. 57, no. 68

    2021  

    Abstract: A new method for the fluorine-18 labelling of trifluoromethyl ketones has been developed. This method is based on the conversion of a–COCF₃ functional group to a difluoro enol silyl ether followed by halogenation and fluorine-18 labelling. The utility of ...

    Abstract A new method for the fluorine-18 labelling of trifluoromethyl ketones has been developed. This method is based on the conversion of a–COCF₃ functional group to a difluoro enol silyl ether followed by halogenation and fluorine-18 labelling. The utility of this new method was demonstrated by the synthesis of fluorine-18 labelled neutrophil elastase inhibitors, which are potentially useful for detection of inflammatory disorders.
    Schlagwörter elastase ; enols ; neutrophils
    Sprache Englisch
    Erscheinungsverlauf 2021-0825
    Umfang p. 8476-8479.
    Erscheinungsort The Royal Society of Chemistry
    Dokumenttyp Artikel
    ZDB-ID 1472881-3
    ISSN 1364-548X ; 1359-7345 ; 0009-241X
    ISSN (online) 1364-548X
    ISSN 1359-7345 ; 0009-241X
    DOI 10.1039/d1cc03624f
    Datenquelle NAL Katalog (AGRICOLA)

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  3. Artikel ; Online: Base-catalysed

    Meyer, Denise N / Cortés González, Miguel A / Jiang, Xingguo / Johansson-Holm, Linus / Pourghasemi Lati, Monireh / Elgland, Mathias / Nordeman, Patrik / Antoni, Gunnar / Szabó, Kálmán J

    Chemical communications (Cambridge, England)

    2021  Band 57, Heft 68, Seite(n) 8476–8479

    Abstract: A new method for the fluorine-18 labelling of trifluoromethyl ketones has been developed. This method is based on the conversion of a- ... ...

    Abstract A new method for the fluorine-18 labelling of trifluoromethyl ketones has been developed. This method is based on the conversion of a-COCF
    Mesh-Begriff(e) Fluorine Radioisotopes/chemistry ; Ketones/chemistry ; Molecular Structure ; Proteinase Inhibitory Proteins, Secretory/chemical synthesis ; Proteinase Inhibitory Proteins, Secretory/chemistry
    Chemische Substanzen Fluorine Radioisotopes ; Ketones ; Proteinase Inhibitory Proteins, Secretory ; Fluorine-18 (GZ5I74KB8G)
    Sprache Englisch
    Erscheinungsdatum 2021-08-04
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 1472881-3
    ISSN 1364-548X ; 1359-7345 ; 0009-241X
    ISSN (online) 1364-548X
    ISSN 1359-7345 ; 0009-241X
    DOI 10.1039/d1cc03624f
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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