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Browsing by Author "Bauer, Michaela"

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Now showing 1 - 4 of 4
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    C–H arylations of 1,2,3-triazoles by reusable heterogeneous palladium catalysts in biomass-derived γ-valerolactone
    (Royal Soc Chemistry, 2016)
    Tian, Xu
    ;
    Yang, Fanzhi
    ;
    Rasina, Dace
    ;
    Bauer, Michaela
    ;
    Warratz, Svenja  
    ;
    Ferlin, Francesco
    ;
    Vaccaro, Luigi
    ;
    Ackermann, Lutz  
    C–H arylations were accomplished with a user-friendly heterogeneous palladium catalyst in the biomass-derived c-valerolactone (GVL) as an environmentally-benign reaction medium. The userfriendly protocol was characterized by ample substrate scope and high functional group tolerance in the C–H arylation of 1,2,3- triazoles, and the palladium catalyst could be recycled and reused in the C–H activation process.
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    Internal Peptide Late-Stage Diversification: Peptide-Isosteric Triazoles for Primary and Secondary C(sp 3 )−H Activation
    (2017)
    Bauer, Michaela
    ;
    Wang, Wei
    ;
    Lorion, Mélanie M.  
    ;
    Dong, Chuan
    ;
    Ackermann, Lutz  
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    Late-Stage Diversification of Peptides by Metal-Free C-H Arylation
    (Wiley-v C H Verlag Gmbh, 2014)
    Zhu, Y.
    ;
    Bauer, Michaela
    ;
    Ploog, Jasper
    ;
    Ackermann, Lutz  
    The bioorthogonal late-stage diversification of functionalized oligopeptides was accomplished through a metal-free, site-selective C-H arylation of engineered indole derivatives under mild reaction conditions.
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    Late-Stage Peptide Diversification by Bioorthogonal Catalytic CH Arylation at 23 degrees C in H2O
    (Wiley-v C H Verlag Gmbh, 2015)
    Zhu, Y.
    ;
    Bauer, Michaela
    ;
    Ackermann, Lutz  
    The step-economical late-stage diversification of tryptophan-containing peptides was accomplished through chemo- and site-selective palladium-catalyzed CH arylation under exceedingly mild reaction conditions. Thus, the CH functionalization occurred efficiently at 23 degrees C with a catalyst loading as low as 0.5mol%, and/or in H2O.

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