Search Results - "Ligibel, Mathieu"

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  1. 1

    Evolved Aliphatic Halogenases Enable Regiocomplementary C−H Functionalization of a Pharmaceutically Relevant Compound by Hayashi, Takahiro, Ligibel, Mathieu, Sager, Emine, Voss, Moritz, Hunziker, Jürg, Schroer, Kirsten, Snajdrova, Radka, Buller, Rebecca

    Published in Angewandte Chemie International Edition (16-12-2019)
    “…Non‐heme iron halogenases are synthetically valuable biocatalysts that are capable of halogenating unactivated sp3‐hybridized carbon centers with high stereo‐…”
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    Journal Article
  2. 2

    Identification and application of threonine aldolase for synthesis of valuable α-amino, β-hydroxy-building blocks by Ligibel, Mathieu, Moore, Charles, Bruccoleri, Robert, Snajdrova, Radka

    “…Chiral β-hydroxy α-amino acid structural motifs are interesting and common synthons present in multiple APIs and drug candidates. To access these chiral…”
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    Enzyme Engineering Enables Inversion of Substrate Stereopreference of the Halogenase WelO5 by Voss, Moritz, Hüppi, Sean, Schaub, Daniela, Hayashi, Takahiro, Ligibel, Mathieu, Sager, Emine, Schroer, Kirsten, Snajdrova, Radka, Buller, Rebecca

    Published in ChemCatChem (20-12-2022)
    “…Enzymatic late‐stage diversification of small molecules has the potential to rapidly generate diversity in compound libraries dedicated to drug discovery. In…”
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    Journal Article
  6. 6

    Cover Picture: Evolved Aliphatic Halogenases Enable Regiocomplementary C−H Functionalization of a Pharmaceutically Relevant Compound (Angew. Chem. Int. Ed. 51/2019) by Hayashi, Takahiro, Ligibel, Mathieu, Sager, Emine, Voss, Moritz, Hunziker, Jürg, Schroer, Kirsten, Snajdrova, Radka, Buller, Rebecca

    Published in Angewandte Chemie International Edition (16-12-2019)
    “…Tailored aliphatic halogenases enable the derivatization of unactivated carbon centers in non‐native substrates with exquisite stereo‐ and regioselectivity. In…”
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    Journal Article
  7. 7

    Front Cover: Enzyme Engineering Enables Inversion of Substrate Stereopreference of the Halogenase WelO5 (ChemCatChem 24/2022) by Voss, Moritz, Hüppi, Sean, Schaub, Daniela, Hayashi, Takahiro, Ligibel, Mathieu, Sager, Emine, Schroer, Kirsten, Snajdrova, Radka, Buller, Rebecca

    Published in ChemCatChem (20-12-2022)
    “…The Front Cover depicts the opportunity to selectively chlorinate distinct stereoisomers of a bioactive molecule through the choice between tailored…”
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    Journal Article
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    Titelbild: Evolvierte aliphatische Halogenasen ermöglichen die regiokomplementäre C‐H‐Funktionalisierung einer hochwertigen Chemikalie (Angew. Chem. 51/2019) by Hayashi, Takahiro, Ligibel, Mathieu, Sager, Emine, Voss, Moritz, Hunziker, Jürg, Schroer, Kirsten, Snajdrova, Radka, Buller, Rebecca

    Published in Angewandte Chemie (16-12-2019)
    “…Maßgeschneiderte aliphatische Halogenasen ermöglichen die Derivatisierung nichtaktivierter Kohlenstoffzentren in nichtnativen Substraten mit hoher Stereo‐ und…”
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    Journal Article
  10. 10

    Evolvierte aliphatische Halogenasen ermöglichen die regiokomplementäre C‐H‐Funktionalisierung einer hochwertigen Chemikalie by Hayashi, Takahiro, Ligibel, Mathieu, Sager, Emine, Voss, Moritz, Hunziker, Jürg, Schroer, Kirsten, Snajdrova, Radka, Buller, Rebecca

    Published in Angewandte Chemie (16-12-2019)
    “…Nicht‐Häm‐Eisen(II)‐Halogenasen sind wertvolle Biokatalysatoren für die stereo‐ und enantioselektive Halogenierung von nicht‐aktivierten sp3‐Kohlenstoffatomen…”
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    Journal Article