@article{UrlaubKaiserScherf‐Claveletal.2021,
  author    = {Urlaub, Jonas and Kaiser, Reinhard P. and Scherf-Clavel, Oliver and Bolm, Carsten and Holzgrabe, Ulrike},
  title     = {Investigation of isomerization of dexibuprofen in a ball mill using chiral capillary electrophoresis},
  series = {Electrophoresis},
  volume    = {42},
  journal   = {Electrophoresis},
  number    = {17-18},
  doi       = {10.1002/elps.202000307},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-225852},
  pages     = {1790 -- 1799},
  year      = {2021},
  abstract  = {Besides the racemate, the S-enantiomer of ibuprofen (Ibu) is used for the treatment of inflammation and pain. Since the configurational stability of S-Ibu in solid state is of interest, it was studied by means of ball milling experiments. For the evaluation of the enantiomeric composition, a chiral CE method was developed and validated according to the ICH guideline Q2(R1). The addition of Mg\(^{2+}\), Ca\(^{2+}\), or Zn\(^{2+}\) ions to the background electrolyte (BGE) was found to improve Ibu enantioresolution. Chiral separation of Ibu enantiomers was achieved on a 60.2 cm (50.0 cm effective length) x 75 μm fused-silica capillary using a background electrolyte (BGE) composed of 50 mM sodium acetate, 10 mM magnesium acetate tetrahydrate, and 35 mM heptakis-(2,3,6-tri-O-methyl)-β-cyclodextrin (TM-β-CD) as chiral selector. The quantification of R-Ibu in the mixture was performed using the normalization procedure. Linearity was evaluated in the range of 0.68-5.49\% R-Ibu (R\(^{2}\) = 0.999), recovery was found to range between 97 and 103\%, the RSD of intra- and interday precision below 2.5\%, and the limit of quantification for R- in S-Ibu was calculated to be 0.21\% (extrapolated) and 0.15\% (dilution of racemic ibuprofen), respectively. Isomerization of S-Ibu was observed under basic conditions by applying long milling times and high milling frequencies.},
  language  = {en}
}
@article{LindlGuoKrummenacheretal.2021,
  author    = {Lindl, Felix and Guo, Xueying and Krummenacher, Ivo and Rauch, Florian and Rempel, Anna and Paprocki, Valerie and Dellermann, Theresa and Stennett, Tom E. and Lamprecht, Anna and Br{\"u}ckner, Tobias and Radacki, Krzysztof and B{\´e}langer-Chabot, Guillaume and Marder, Todd B. and Lin, Zhenyang and Braunschweig, Holger},
  title     = {Rethinking Borole Cycloaddition Reactivity},
  series = {Chemistry—A European Journal},
  volume    = {27},
  journal   = {Chemistry—A European Journal},
  number    = {43},
  doi       = {10.1002/chem.202101290},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-256888},
  pages     = {11226-11233},
  year      = {2021},
  abstract  = {Boroles are attracting broad interest for their myriad and diverse applications, including in synthesis, small molecule activation and functional materials. Their properties and reactivity are closely linked to the cyclic conjugated diene system, which has been shown to participate in cycloaddition reactions, such as the Diels-Alder reaction with alkynes. The reaction steps leading to boranorbornadienes, borepins and tricyclic boracyclohexenes from the thermal reaction of boroles with alkynes are seemingly well understood as judged from the literature. Herein, we question the long-established mechanistic picture of pericyclic rearrangements by demonstrating that seven-membered borepins (i. e., heptaphenylborepin and two derivatives substituted with a thienyl and chloride substituent on boron) exist in a dynamic equilibrium with the corresponding bicyclic boranorbornadienes, the direct Diels-Alder products, but are not isolable products from the reactions. Heating gradually converts the isomeric mixtures into fluorescent tricyclic boracyclohexenes, the most stable isomers in the series. Results from mechanistic DFT calculations reveal that the tricyclic compounds derive from the boranorbornadienes and not the borepins, which were previously believed to be intermediates in purely pericyclic processes.},
  language  = {en}
}