@misc{PapeWessigBrunner2015,
  author    = {Pape, Simon and Wessig, Pablo and Brunner, Heiko},
  title     = {A new and environmentally benign synthesis of aroylguanidines using iron trichloride},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-102720},
  pages     = {101408 -- 101411},
  year      = {2015},
  abstract  = {A new synthetic approach for the guanylation of aroylthioureas using iron trichloride is presented. Our synthetic method distinguishes itself by benign reaction conditions, low costs and a broad product spectrum. The scope of the reaction and calorimetric studies are described.},
  language  = {en}
}
@article{PapeWessigBrunner2015,
  author    = {Pape, Simon and Wessig, Pablo and Brunner, Heiko},
  title     = {A new and environmentally benign synthesis of aroylguanidines using iron trichloride},
  series = {RSC Advances},
  volume    = {5},
  journal   = {RSC Advances},
  number    = {123},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {2046-2069},
  doi       = {10.1039/c5ra20869f},
  pages     = {101408 -- 101411},
  year      = {2015},
  abstract  = {A new synthetic approach for the guanylation of aroylthioureas using iron trichloride is presented. Our synthetic method distinguishes itself by benign reaction conditions, low costs and a broad product spectrum. The scope of the reaction and calorimetric studies are described.},
  language  = {en}
}
@phdthesis{Pape2016,
  author    = {Pape, Simon},
  title     = {Entwicklung und Evaluierung von Methoden zur Synthese neuartiger Additive f{\"u}r die außenstromlose Nickel-Phosphor-Abscheidung},
  school      = {Universit{\"a}t Potsdam},
  pages     = {223},
  year      = {2016},
  language  = {de}
}
@article{PapeWessigBrunner2016,
  author    = {Pape, Simon and Wessig, Pablo and Brunner, Heiko},
  title     = {Iron Trichloride and Air Mediated Guanylation of Acylthioureas. An Ecological Route to Acylguanidines: Scope and Mechanistic Insights},
  series = {The journal of organic chemistry},
  volume    = {81},
  journal   = {The journal of organic chemistry},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {0022-3263},
  doi       = {10.1021/acs.joc.6b00600},
  pages     = {4701 -- 4712},
  year      = {2016},
  abstract  = {Recently we introduced iron trichloride as an environmentally benign and cost-efficient reagent for the synthesis of N-benzoylguanidines. This highly attractive synthetic approach grants access to a broad spectrum of N-benzoylguanidines under mild conditions in short reaction times. In this work we present an extended scope of Our methodology along with the results obtained from mechanistic studies via in situ IR spectroscopy in combination with LC (liquid chromatography)-MS analyses. On the basis of these new mechanistic insights we were able to optimize the synthetic protocol and to develop an alternative mechanistic proposal. In this context the symbiotic roles of iron trithloride and oxygen in the guanylation process are highlighted.},
  language  = {en}
}
@article{WessigGerngrossPapeetal.2014,
  author    = {Wessig, Pablo and Gerngroß, Maik and Pape, Simon and Bruhns, Philipp and Weber, Jens},
  title     = {Novel porous materials based on oligospiroketals (OSK)},
  series = {RSC Advances : an international journal to further the chemical sciences},
  volume    = {2014},
  journal   = {RSC Advances : an international journal to further the chemical sciences},
  number    = {4},
  issn      = {2046-2069},
  doi       = {10.1039/c4ra04437a},
  pages     = {31123 -- 31129},
  year      = {2014},
  abstract  = {New porous materials based on covalently connected monomers are presented. The key step of the synthesis is an acetalisation reaction. In previous years we used acetalisation reactions extensively to build up various molecular rods. Based on this approach, investigations towards porous polymeric materials were conducted by us. Here we wish to present the results of these studies in the synthesis of 1D polyacetals and porous 3D polyacetals. By scrambling experiments with 1D acetals we could prove that exchange reactions occur between different building blocks (evidenced by MALDI-TOF mass spectrometry). Based on these results we synthesized porous 3D polyacetals under the same mild conditions.},
  language  = {en}
}
@misc{WessigGerngrossPapeetal.2014,
  author    = {Wessig, Pablo and Gerngroß, Maik and Pape, Simon and Bruhns, Philipp and Weber, Jens},
  title     = {Novel porous materials based on oligospiroketals (OSK)},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-74466},
  pages     = {31123 -- 31129},
  year      = {2014},
  abstract  = {New porous materials based on covalently connected monomers are presented. The key step of the synthesis is an acetalisation reaction. In previous years we used acetalisation reactions extensively to build up various molecular rods. Based on this approach, investigations towards porous polymeric materials were conducted by us. Here we wish to present the results of these studies in the synthesis of 1D polyacetals and porous 3D polyacetals. By scrambling experiments with 1D acetals we could prove that exchange reactions occur between different building blocks (evidenced by MALDI-TOF mass spectrometry). Based on these results we synthesized porous 3D polyacetals under the same mild conditions.},
  language  = {en}
}
@article{WessigGerngrossPapeetal.2014,
  author    = {Wessig, Pablo and Gerngross, Maik and Pape, Simon and Bruhns, Philipp and Weber, Jens},
  title     = {Novel porous materials based on oligospiroketals (OSK)},
  series = {RSC Advances},
  volume    = {4},
  journal   = {RSC Advances},
  number    = {59},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {2046-2069},
  doi       = {10.1039/c4ra04437a},
  pages     = {31123 -- 31129},
  year      = {2014},
  abstract  = {New porous materials based on covalently connected monomers are presented. The key step of the synthesis is an acetalisation reaction. In previous years we used acetalisation reactions extensively to build up various molecular rods. Based on this approach, investigations towards porous polymeric materials were conducted by us. Here we wish to present the results of these studies in the synthesis of 1D polyacetals and porous 3D polyacetals. By scrambling experiments with 1D acetals we could prove that exchange reactions occur between different building blocks (evidenced by MALDI-TOF mass spectrometry). Based on these results we synthesized porous 3D polyacetals under the same mild conditions.},
  language  = {en}
}