Search Results - "Burdack, Christoph"

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  1. 1

    Highly substituted indol-2-ones, quinoxalin-2-ones and benzodiazepin-2,5-diones via a new Ugi(4CR)-Pd assisted N-aryl amidation strategy by Kalinski, Cédric, Umkehrer, Michael, Ross, Günther, Kolb, Jürgen, Burdack, Christoph, Hiller, Wolfgang

    Published in Tetrahedron letters (15-05-2006)
    “…A new strategy employing an Ugi four-component reaction and a palladium-assisted intramolecular N-aryl amidation reaction is reported. The straight forward…”
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  2. 2

    A novel one-pot synthesis of highly diverse indole scaffolds by the Ugi/Heck reaction by Kalinski, Cédric, Umkehrer, Michael, Schmidt, Jürgen, Ross, Günther, Kolb, Jürgen, Burdack, Christoph, Hiller, Wolfgang, Hoffmann, Stephan D.

    Published in Tetrahedron letters (03-07-2006)
    “…A novel one-pot two-step multi component reaction of acrylic aldehydes, bromoanilines, acids and isocyanides yielding polysubstituted indoles is described. The…”
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  3. 3

    Tetramic acid derivatives via Ugi–Dieckmann-reaction by Spatz, Julia H., Welsch, Sebastian J., Duhaut, David-Emmanuel, Jäger, Nadine, Boursier, Thomas, Fredrich, Martin, Allmendinger, Lars, Ross, Günther, Kolb, Jürgen, Burdack, Christoph, Umkehrer, Michael

    Published in Tetrahedron letters (15-04-2009)
    “…Tetramic acid derivatives constitute an important class of nitrogen containing heterocycles, and are key structural motifs in many natural products of…”
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  4. 4

    Pd II/IV catalyzed oxidative cyclization of 1,6-enynes derived by Ugi-4-component reaction by Welsch, Sebastian J., Umkehrer, Michael, Ross, Günther, Kolb, Jürgen, Burdack, Christoph, Wessjohann, Ludger A.

    Published in Tetrahedron letters (23-11-2011)
    “…A variety of 1,6-enynes were synthesized by an Ugi-reaction and further elaborated by a Pd II/IV catalyzed oxidative cyclization to produce N-substituted…”
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  5. 5

    A new and versatile one-pot synthesis of indol-2-ones by a novel Ugi-four-component-Heck reaction by Umkehrer, Michael, Kalinski, Cédric, Kolb, Jürgen, Burdack, Christoph

    Published in Tetrahedron letters (03-04-2006)
    “…A novel one-pot-synthesis of highly substituted indol-2-ones using a combination of Ugi and Heck reaction (U-4CR-Heck) is described. The synthesized…”
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  6. 6

    Synthesis of substituted imidazolines by an Ugi/Staudinger/aza-Wittig sequence by Welsch, Sebastian J., Umkehrer, Michael, Kalinski, Cedric, Ross, Günther, Burdack, Christoph, Kolb, Jürgen, Wild, Martina, Ehrlich, Anja, Wessjohann, Ludger A.

    Published in Tetrahedron letters (18-02-2015)
    “…[Display omitted] A series of 2-(acetamide-2-yl)-imidazolines (II) with 5 points of diversity were prepared by an Ugi-4CR–Staudinger–aza-Wittig-sequence…”
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  7. 7

    On the industrial applications of MCRs: molecular diversity in drug discovery and generic drug synthesis by Kalinski, Cédric, Umkehrer, Michael, Weber, Lutz, Kolb, Jürgen, Burdack, Christoph, Ross, Günther

    Published in Molecular diversity (01-08-2010)
    “…During the last decades, multicomponent chemistry has gained much attention in pharmaceutical research, especially in the context of lead finding and…”
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  8. 8

    Palladium and copper catalyzed cyclizations of hydrazine derived Ugi products: facile synthesis of substituted indazolones and hydroxytriazafluorendiones by Welsch, Sebastian J., Kalinski, Cédric, Umkehrer, Michael, Ross, Günther, Kolb, Jürgen, Burdack, Christoph, Wessjohann, Ludger A.

    Published in Tetrahedron letters (02-05-2012)
    “…Indazolones are medicinally relevant targets. Herein we disclose an improved synthesis to N′-(acetamido-2-yl)-substituted indazolones with four points of…”
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  9. 9

    Pd super(II/IV catalyzed oxidative cyclization of 1,6-enynes derived by Ugi-4-component reaction) by Welsch, Sebastian J, Umkehrer, Michael, Ross, Guenther, Kolb, Juergen, Burdack, Christoph, Wessjohann, Ludger A

    Published in Tetrahedron letters (23-11-2011)
    “…A variety of 1,6-enynes were synthesized by an Ugi-reaction and further elaborated by a Pd super(II/IV catalyzed oxidative cyclization to produce N-substituted…”
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  10. 10
  11. 11

    Expeditious synthesis of imidazo[1,2- c]pyrimidines via a [4+1]-cycloaddition by Umkehrer, Michael, Ross, Günther, Jäger, Nadine, Burdack, Christoph, Kolb, Jürgen, Hu, Hong, Alvim-Gaston, Maria, Hulme, Christopher

    Published in Tetrahedron letters (19-03-2007)
    “…A new and versatile synthesis of imidazo[1,2- c]pyrimidines via a [4+1]-cycloaddition is described. The reported novel synthetic approach leads to…”
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  12. 12

    Synthesis of tetrazolopiperazine building blocks by a novel multi-component reaction by Umkehrer, Michael, Kolb, Jürgen, Burdack, Christoph, Ross, Günther, Hiller, Wolfgang

    Published in Tetrahedron letters (16-08-2004)
    “…[Display omitted] A novel Ugi-five-centre-four-component reaction (U-5C-4CR) of aldehydes, primary amines, trimethylsilylazide and 2-isocyanoethyltosylate…”
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  13. 13
  14. 14

    New cleavable isocyanides for the combinatorial synthesis of α-amino acid analogue tetrazoles by Mayer, Josef, Umkehrer, Michael, Kalinski, Cédric, Ross, Günther, Kolb, Jürgen, Burdack, Christoph, Hiller, Wolfgang

    Published in Tetrahedron letters (24-10-2005)
    “…3-Substituted 3-isocyano propionates as new cleavable isocyanides in combinatorial tetrazole synthesis via Ugi-reaction are introduced. The obtained…”
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  15. 15

    Combinatorial synthesis of 4-oxo-4 H-imidazo[1,5- a]quinoxalines and 4-oxo-4 H-pyrazolo[1,5- a]quinoxalines by Spatz, Julia H., Umkehrer, Michael, Kalinski, Cédric, Ross, Günther, Burdack, Christoph, Kolb, Jürgen, Bach, Thorsten

    Published in Tetrahedron letters (2007)
    “…A combinatorial synthetic route yielding imidazo[1,5- a]quinoxalines and pyrazolo[1,5- a]quinoxalines is described. The use of 2-fluoroaniline and 1…”
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  16. 16

    Diversity oriented synthesis of benzoxazoles and benzothiazoles by Spatz, Julia H., Bach, Thorsten, Umkehrer, Michael, Bardin, Julien, Ross, Günther, Burdack, Christoph, Kolb, Jürgen

    Published in Tetrahedron letters (17-12-2007)
    “…A combinatorial synthetic route yielding benzoxazoles and benzothiazoles is described. The use of o-halophenylisocyanides in the Ugi reaction (U-4CR) followed…”
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