@article{11988,
  abstract     = {A continuous Bucherer–Bergs hydantoin synthesis utilizing intensified conditions is reported. The methodology is characterized by a two-feed flow approach to independently feed the organic substrate and the aqueous reagent solution. The increased interfacial area of the biphasic reaction mixture and the lack of headspace enabled almost quantitative conversions within ca. 30 minutes at 120 °C and 20 bar even for unpolar starting materials. In addition, a selective N(3)-monoalkylation of the resulting heterocycles under batch microwave conditions is reported yielding potential acetylcholinesterase inhibitors.},
  author       = {Kappe, C. and Monteiro, Julia and Pieber, Bartholomäus and Corrêa, Arlene},
  issn         = {1437-2096},
  journal      = {Synlett},
  number       = {01},
  pages        = {83--87},
  publisher    = {Georg Thieme Verlag},
  title        = {{Continuous synthesis of hydantoins: Intensifying the Bucherer–Bergs reaction}},
  doi          = {10.1055/s-0035-1560317},
  volume       = {27},
  year         = {2016},
}

@article{13405,
  abstract     = {We report a method for preparing electrode–molecule–electrode junctions that incorporate nonsymmetrical azobenzene dithiols. Our approach is based on sequential deprotection of thiol moieties originally carrying two different protecting groups. The azobenzene derivatives retained their switching properties within monolayers and permitted the photocontrol of electrical conductance.},
  author       = {Ely, Tal and Das, Sanjib and Li, Wenjie and Kundu, Pintu and Tirosh, Einat and Cahen, David and Vilan, Ayelet and Klajn, Rafal},
  issn         = {1437-2096},
  journal      = {Synlett},
  keywords     = {Organic Chemistry},
  number       = {18},
  pages        = {2370--2374},
  publisher    = {Georg Thieme Verlag},
  title        = {{Photocontrol of electrical conductance with a nonsymmetrical azobenzene dithiol}},
  doi          = {10.1055/s-0033-1340087},
  volume       = {24},
  year         = {2013},
}

@article{13437,
  abstract     = {Liquid/liquid Phase Transfer Catalysis (PTC) reaction of 4-chlorobutyronitrile with nonenolisable aldehydes leads via an addition-cyclisation reaction sequence to derivatives of tetrahydrofuran-3-carbonitrile.},
  author       = {Macogonkosza, Mieczysław and Przyborowski, Jacek and Klajn, Rafal and Kwast, Andrzej},
  issn         = {1437-2096},
  journal      = {Synlett},
  keywords     = {Organic Chemistry},
  number       = {12},
  pages        = {1773--1774},
  publisher    = {Georg Thieme Verlag},
  title        = {{Simple synthesis of 2-substituted Tetrahydrofuran-3-carbonitriles}},
  doi          = {10.1055/s-2000-8670},
  volume       = {2000},
  year         = {2000},
}