Skip to main content

and
  1. No Access

    Article

    Biocatalytic, enantioenriched primary amination of tertiary C–H bonds

    Intermolecular functionalization of tertiary C–H bonds to construct fully substituted stereogenic carbon centres represents a formidable challenge: without the assistance of directing groups, state-of-the-art ...

    Runze Mao, Shilong Gao, Zi-Yang Qin, Torben Rogge, Sophia J. Wu in Nature Catalysis (2024)

  2. No Access

    Article

    Biocatalytic, stereoconvergent alkylation of (Z/E)-trisubstituted silyl enol ethers

    The selective conversion of mixtures of Z/E alkenes into chiral products is a synthetic challenge. Biocatalytic strategies can transform isomeric alkenes into stereopure compounds, but enzymes typically convert o...

    Runze Mao, Doris Mia Taylor, Daniel J. Wackelin, Torben Rogge in Nature Synthesis (2024)

  3. Article

    Open Access

    Data-driven design of new chiral carboxylic acid for construction of indoles with C-central and C–N axial chirality via cobalt catalysis

    Challenging enantio- and diastereoselective cobalt-catalyzed C–H alkylation has been realized by an innovative data-driven knowledge transfer strategy. Harnessing the statistics of a related transformation as ...

    Zi-**g Zhang, Shu-Wen Li, João C. A. Oliveira, Yanjun Li in Nature Communications (2023)

  4. No Access

    Article

    C–H activation

    Transition metal-catalysed C–H activation has emerged as an increasingly powerful platform for molecular syntheses, enabling applications to natural product syntheses, late-stage modification, pharmaceutical i...

    Torben Rogge, Nikolaos Kaplaneris, Naoto Chatani in Nature Reviews Methods Primers (2021)

  5. Article

    Open Access

    Late-stage peptide C–H alkylation for bioorthogonal C–H activation featuring solid phase peptide synthesis

    Methods for the late-stage diversification of structurally complex peptides hold enormous potential for advances in drug discovery, agrochemistry and pharmaceutical industries. While C–H arylations emerged for...

    Alexandra Schischko, Nikolaos Kaplaneris, Torben Rogge in Nature Communications (2019)

  6. No Access

    Article

    Versatile and robust C–C activation by chelation-assisted manganese catalysis

    C–H activation has been recognized as an increasingly viable tool in molecular sciences, but organometallic C–C activation is scarce, and limited to precious and toxic metal catalysts. Herein, we disclose vers...

    Hui Wang, Isaac Choi, Torben Rogge, Nikolaos Kaplaneris, Lutz Ackermann in Nature Catalysis (2018)

  7. Article

    Open Access

    Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides

    Chalcogen-containing compounds have received considerable attention because of their manifold applications in agrochemicals, pharmaceuticals, and material science. While many classical methods have been develo...

    Yi Fang, Torben Rogge, Lutz Ackermann, Shun-Yi Wang, Shun-Jun Ji in Nature Communications (2018)

  8. Article

    Open Access

    Ruthenium(II)-catalysed remote C–H alkylations as a versatile platform to meta-decorated arenes

    The full control of positional selectivity is of prime importance in C–H activation technology. Chelation assistance served as the stimulus for the development of a plethora of ortho-selective arene functionaliza...

    Jie Li, Korkit Korvorapun, Suman De Sarkar, Torben Rogge in Nature Communications (2017)