Tanja Gulder

Summary

Affiliation: RWTH Aachen
Country: Germany

Publications

  1. doi Halocarbocyclization versus dihalogenation: substituent directed iodine(iii) catalyzed halogenations
    Maciej Stodulski
    Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, D 52056 Aachen, Germany
    Chem Commun (Camb) 50:3435-8. 2014
  2. doi Strained cyclophane natural products: macrocyclization at its limits
    Tanja Gulder
    RWTH Aachen University, Institute of Organic Chemistry, Landoltweg 1, 52056 Aachen, Germany
    Nat Prod Rep 29:899-934. 2012
  3. pmc Modeling antibiotic and cytotoxic effects of the dimeric isoquinoline IQ-143 on metabolism and its regulation in Staphylococcus aureus, Staphylococcus epidermidis and human cells
    Alexander Cecil
    University of Wurzburg, Theodor Boveri Institute, Department of Bioinformatics, Am Hubland, 97074 Wurzburg, Germany
    Genome Biol 12:R24. 2011
  4. doi Nanoparticles and peptides: a fruitful liaison for biomimetic catalysis
    Maciej Stodulski
    Institute of Organic Chemistry, RWTH Aachen University, Germany
    Angew Chem Int Ed Engl 51:11202-4. 2012
  5. doi Metal-free synthesis of 3,3-disubstituted oxoindoles by iodine(III)-catalyzed bromocarbocyclizations
    David C Fabry
    Institute of Organic Chemistry, RWTH Aachen, Aachen, Germany
    Chemistry 18:10834-8. 2012

Collaborators

  • Maciej Stodulski
  • David C Fabry
  • Alexander Cecil
  • Stefanie V Kohlhepp
  • Alissa Goetzinger
  • Stefanie Hoerner
  • Tobias A Oelschlaeger
  • Gerhard Bringmann
  • Ulrike Holzgrabe
  • Thomas Dandekar
  • Jörg Bernhardt
  • Carina Rikanović
  • Matthias Unger
  • Chunguang Liang
  • Knut Ohlsen

Detail Information

Publications5

  1. doi Halocarbocyclization versus dihalogenation: substituent directed iodine(iii) catalyzed halogenations
    Maciej Stodulski
    Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, D 52056 Aachen, Germany
    Chem Commun (Camb) 50:3435-8. 2014
    ..Utilizing this catalyst-dependent reactivity a diastereo- and chemoselective dihalogenation method was established allowing the conversion of structurally and electronically diverse unsaturated compounds in excellent yields. ..
  2. doi Strained cyclophane natural products: macrocyclization at its limits
    Tanja Gulder
    RWTH Aachen University, Institute of Organic Chemistry, Landoltweg 1, 52056 Aachen, Germany
    Nat Prod Rep 29:899-934. 2012
    ..The main focus will be on the different concepts for the installation of the macrocyclic system, in most cases the central problem in assembling these extremely rigid molecules...
  3. pmc Modeling antibiotic and cytotoxic effects of the dimeric isoquinoline IQ-143 on metabolism and its regulation in Staphylococcus aureus, Staphylococcus epidermidis and human cells
    Alexander Cecil
    University of Wurzburg, Theodor Boveri Institute, Department of Bioinformatics, Am Hubland, 97074 Wurzburg, Germany
    Genome Biol 12:R24. 2011
    ..Here, we demonstrate the utility of complementary analysis of both host and pathogen datasets in assessing bacterial adaptation to IQ-143, a synthetic analog of the novel type N,C-coupled naphthyl-isoquinoline alkaloid ancisheynine...
  4. doi Nanoparticles and peptides: a fruitful liaison for biomimetic catalysis
    Maciej Stodulski
    Institute of Organic Chemistry, RWTH Aachen University, Germany
    Angew Chem Int Ed Engl 51:11202-4. 2012
    ..The concerted interplay of the multivalent surface with the catalytically active peptide and the substrate at the same time combines several aspects decisive for the catalyst's efficiency, a property characteristic of enzymes...
  5. doi Metal-free synthesis of 3,3-disubstituted oxoindoles by iodine(III)-catalyzed bromocarbocyclizations
    David C Fabry
    Institute of Organic Chemistry, RWTH Aachen, Aachen, Germany
    Chemistry 18:10834-8. 2012
    ..The indole-2-ones obtained can be converted easily into structurally complex target compounds, such as the alkaloid physostigmine...