@article{37970,
  author       = {{Longwitz, Lars and Steinbauer, Johannes and Spannenberg, Anke and Werner, Thomas}},
  issn         = {{2155-5435}},
  journal      = {{ACS Catalysis}},
  keywords     = {{T1, T3, T4}},
  number       = {{1}},
  pages        = {{665--672}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions}}},
  doi          = {{10.1021/acscatal.7b03367}},
  volume       = {{8}},
  year         = {{2017}},
}

@article{37979,
  author       = {{Straub, Bernd F. and Andexer, Jennifer and Arenz, Christoph and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ditrich, Klaus and Gulder, Tobias A. M. and Hüttel, Wolfgang and Kordes, Markus and Krueger, Anke and Lehmann, Matthias and Lindel, Thomas and Luy, Burkhard and Meier, Michael A. R. and Mück-Lichtenfeld, Christian and Muhle-Goll, Claudia and Müller, Thomas J. J. and Narine, Arun and Paradies, Jan and Pfau, Roland and Pietruszka, Jörg and Schaschke, Norbert and Senge, Mathias O. and Werner, Thomas and Werz, Daniel B. and Winter, Christian A. and Worgull, Dennis}},
  issn         = {{1439-9598}},
  journal      = {{Nachrichten aus der Chemie}},
  keywords     = {{General Chemical Engineering, General Chemistry}},
  number       = {{3}},
  pages        = {{266--304}},
  publisher    = {{Wiley}},
  title        = {{{Organische Chemie 2016}}},
  doi          = {{10.1002/nadc.20174059831}},
  volume       = {{65}},
  year         = {{2017}},
}

@article{37976,
  author       = {{Li, Wu and Werner, Thomas}},
  issn         = {{1523-7060}},
  journal      = {{Organic Letters}},
  keywords     = {{CSSD}},
  number       = {{10}},
  pages        = {{2568--2571}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles}}},
  doi          = {{10.1021/acs.orglett.7b00720}},
  volume       = {{19}},
  year         = {{2017}},
}

@article{37973,
  abstract     = {{<p>An immobilized bifunctional phosphonium salt catalyst efficiently catalyzed the synthesis of cyclic carbonates under mild conditions, and was reused up to 15 times.</p>}},
  author       = {{Steinbauer, J. and Longwitz, L. and Frank, M. and Epping, J. and Kragl, U. and Werner, Thomas}},
  issn         = {{1463-9262}},
  journal      = {{Green Chemistry}},
  keywords     = {{T1, T2, CSSD}},
  number       = {{18}},
  pages        = {{4435--4445}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides}}},
  doi          = {{10.1039/c7gc01782k}},
  volume       = {{19}},
  year         = {{2017}},
}

@article{37975,
  abstract     = {{<p>Calcium punched beyond its weight: An <italic>in situ</italic> formed Ca<sup>2+</sup>–crown ether complex showed unprecedented efficiency in cyclic carbonate synthesis.</p>}},
  author       = {{Steinbauer, J. and Spannenberg, A. and Werner, Thomas}},
  issn         = {{1463-9262}},
  journal      = {{Green Chemistry}},
  keywords     = {{T1, T3, CSSD}},
  number       = {{16}},
  pages        = {{3769--3779}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides}}},
  doi          = {{10.1039/c7gc01114h}},
  volume       = {{19}},
  year         = {{2017}},
}

@article{37977,
  author       = {{Büttner, Hendrik and Longwitz, Lars and Steinbauer, Johannes and Wulf, Christoph and Werner, Thomas}},
  issn         = {{2365-0869}},
  journal      = {{Topics in Current Chemistry}},
  keywords     = {{T1, CSSD}},
  number       = {{3}},
  publisher    = {{Springer Science and Business Media LLC}},
  title        = {{{Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2}}},
  doi          = {{10.1007/s41061-017-0136-5}},
  volume       = {{375}},
  year         = {{2017}},
}

@article{37972,
  author       = {{Li, Wu and Wang, Ming-Ming and Hu, Yuya and Werner, Thomas}},
  issn         = {{1523-7060}},
  journal      = {{Organic Letters}},
  keywords     = {{CSSD}},
  number       = {{21}},
  pages        = {{5768--5771}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds}}},
  doi          = {{10.1021/acs.orglett.7b02701}},
  volume       = {{19}},
  year         = {{2017}},
}

@article{37978,
  author       = {{Büttner, Hendrik and Steinbauer, Johannes and Wulf, Christoph and Dindaroglu, Mehmet and Schmalz, Hans-Günther and Werner, Thomas}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{T1, T2, CSSD}},
  number       = {{6}},
  pages        = {{1076--1079}},
  publisher    = {{Wiley}},
  title        = {{{Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables}}},
  doi          = {{10.1002/cssc.201601163}},
  volume       = {{10}},
  year         = {{2017}},
}

@article{37974,
  author       = {{Steinbauer, Johannes and Werner, Thomas}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{T1, T3, CSSD}},
  number       = {{15}},
  pages        = {{3025--3029}},
  publisher    = {{Wiley}},
  title        = {{{Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis}}},
  doi          = {{10.1002/cssc.201700788}},
  volume       = {{10}},
  year         = {{2017}},
}

@article{13412,
  author       = {{Konieczna, Dagny D. and Biller, Harry and Witte, Matthias and Schmidt, Wolf Gero and Neuba, Adam and Wilhelm, René}},
  issn         = {{0040-4020}},
  journal      = {{Tetrahedron}},
  pages        = {{142--149}},
  title        = {{{New pyridinium based ionic dyes for the hydrogen evolution reaction}}},
  doi          = {{10.1016/j.tet.2017.11.053}},
  year         = {{2017}},
}

@article{64888,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>Manche boranbasierten frustrierten Lewis‐Paare spalten Wasserstoff – wie, war bislang unklar. Um Struktur und Reaktivität in Beziehung zu setzen, werden quantenchemische Untersuchungen und NMR‐Experimente kombiniert. Sind pK<jats:sub>a</jats:sub>‐Werte der Lewis‐Base bekannt, lässt sich damit Reaktivität vorhersagen.</jats:p>}},
  author       = {{Paradies, Jan}},
  issn         = {{1439-9598}},
  journal      = {{Nachrichten aus der Chemie}},
  number       = {{2}},
  pages        = {{118--122}},
  publisher    = {{Wiley}},
  title        = {{{Reaktivität verstehen, ohne die Katalysatorstruktur zu kennen}}},
  doi          = {{10.1002/nadc.20174055283}},
  volume       = {{65}},
  year         = {{2017}},
}

@article{64899,
  author       = {{Straub, Bernd F. and Andexer, Jennifer and Arenz, Christoph and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ditrich, Klaus and Gulder, Tobias A. M. and Hüttel, Wolfgang and Kordes, Markus and Krueger, Anke and Lehmann, Matthias and Lindel, Thomas and Luy, Burkhard and Meier, Michael A. R. and Mück-Lichtenfeld, Christian and Muhle-Goll, Claudia and Müller, Thomas J. J. and Narine, Arun and Paradies, Jan and Pfau, Roland and Pietruszka, Jörg and Schaschke, Norbert and Senge, Mathias O. and Werner, Thomas and Werz, Daniel B. and Winter, Christian A. and Worgull, Dennis}},
  issn         = {{1439-9598}},
  journal      = {{Nachrichten aus der Chemie}},
  number       = {{3}},
  pages        = {{266--304}},
  publisher    = {{Wiley}},
  title        = {{{Organische Chemie 2016}}},
  doi          = {{10.1002/nadc.20174059831}},
  volume       = {{65}},
  year         = {{2017}},
}

@inbook{64900,
  author       = {{Paradies, Jan}},
  booktitle    = {{Topics in Organometallic Chemistry}},
  isbn         = {{9783319708041}},
  issn         = {{1436-6002}},
  publisher    = {{Springer International Publishing}},
  title        = {{{Chiral Borane-Based Lewis Acids for Metal Free Hydrogenations}}},
  doi          = {{10.1007/3418_2016_173}},
  year         = {{2017}},
}

@article{35706,
  author       = {{Oechsle, Peter and Hou, Peng and Flörke, Ulrich and Paradies, Jan}},
  issn         = {{1615-4150}},
  journal      = {{Advanced Synthesis &amp; Catalysis}},
  keywords     = {{General Chemistry}},
  number       = {{23}},
  pages        = {{3770--3776}},
  publisher    = {{Wiley}},
  title        = {{{Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence}}},
  doi          = {{10.1002/adsc.201600802}},
  volume       = {{358}},
  year         = {{2016}},
}

@article{35708,
  author       = {{Oechsle, Peter and Hou, Peng and Flörke, Ulrich and Paradies, Jan}},
  issn         = {{1615-4150}},
  journal      = {{Advanced Synthesis &amp; Catalysis}},
  keywords     = {{General Chemistry}},
  number       = {{23}},
  pages        = {{3656--3656}},
  publisher    = {{Wiley}},
  title        = {{{Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016)}}},
  doi          = {{10.1002/adsc.201601149}},
  volume       = {{358}},
  year         = {{2016}},
}

@article{35710,
  author       = {{Tussing, Sebastian and Kaupmees, Karl and Paradies, Jan}},
  issn         = {{0947-6539}},
  journal      = {{Chemistry – A European Journal}},
  keywords     = {{General Chemistry, Catalysis, Organic Chemistry}},
  number       = {{22}},
  pages        = {{7302--7302}},
  publisher    = {{Wiley}},
  title        = {{{Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016)}}},
  doi          = {{10.1002/chem.201601558}},
  volume       = {{22}},
  year         = {{2016}},
}

@article{37983,
  abstract     = {{<p><bold>Taking Control!</bold>The binary catalyst system composed of MoO<sub>3</sub>and an organic phoshponium salt [Bu<sub>4</sub>P]X proved very efficient to produce oleochemical cyclic carbonates from renewables.</p>}},
  author       = {{Tenhumberg, Nils and Büttner, Hendrik and Schäffner, Benjamin and Kruse, Daniela and Blumenstein, Michael and Werner, Thomas}},
  issn         = {{1463-9262}},
  journal      = {{Green Chemistry}},
  keywords     = {{T1, T3, CSSD}},
  number       = {{13}},
  pages        = {{3775--3788}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables}}},
  doi          = {{10.1039/c6gc00671j}},
  volume       = {{18}},
  year         = {{2016}},
}

@article{37989,
  author       = {{Schirmer, Marie-Luis and Jopp, Stefan and Holz, Jens and Spannenberg, Anke and Werner, Thomas}},
  issn         = {{1615-4150}},
  journal      = {{Advanced Synthesis and Catalysis}},
  keywords     = {{T2, CSSD}},
  number       = {{1}},
  pages        = {{26--29}},
  publisher    = {{Wiley}},
  title        = {{{Organocatalyzed Reduction of Tertiary Phosphine Oxides}}},
  doi          = {{10.1002/adsc.201500762}},
  volume       = {{358}},
  year         = {{2016}},
}

@article{37984,
  abstract     = {{<jats:p>The Wittig reaction is a fundamental transformation for the preparation of alkenes from carbonyl compounds and phosphonium ylides. The ylides are prepared prior to the olefination step from the respective phosphonium salts by deprotonation utilizing strong bases. A first free-base catalytic Wittig reaction for the preparation of highly functionalized alkenes was based on tributylphosphane as the catalyst. Subsequently we developed a system employing a phospholene oxide as a pre-catalyst and trimethoxysilane as reducing agent which operates under milder conditions. The title compounds, (<jats:italic>E</jats:italic>)-3-benzylidenepyrrolidine-2,5-dione, C<jats:sub>11</jats:sub>H<jats:sub>9</jats:sub>NO<jats:sub>2</jats:sub>, (I), the methylpyrrolidine derivative, C<jats:sub>12</jats:sub>H<jats:sub>11</jats:sub>NO<jats:sub>2</jats:sub>, (II), and the<jats:italic>tert-</jats:italic>butylpyrrolidine derivative, C<jats:sub>15</jats:sub>H<jats:sub>17</jats:sub>NO<jats:sub>2</jats:sub>, (III), have been synthesized by base-free catalytic Wittig reactions. In the crystal of (I), molecules are linked into centrosymmetric dimers<jats:italic>via</jats:italic>pairs of N—H...O hydrogen bonds. Furthermore, in the crystal structure of (III), there are two molecules in the asymmetric unit, whereas in (I) and (II), only one molecule is present.</jats:p>}},
  author       = {{Schirmer, Marie-Luis and Spannenberg, Anke and Werner, Thomas}},
  issn         = {{2053-2296}},
  journal      = {{Acta Crystallographica Section C Structural Chemistry}},
  keywords     = {{T2}},
  number       = {{6}},
  pages        = {{504--508}},
  publisher    = {{International Union of Crystallography (IUCr)}},
  title        = {{{Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione}}},
  doi          = {{10.1107/s2053229616008159}},
  volume       = {{72}},
  year         = {{2016}},
}

@article{37981,
  abstract     = {{<p>The lithium <italic>tert</italic>-butoxide catalyzed addition of CS<sub>2</sub> to epoxides and thiiranes under mild conditions is reported. A mechanism has been proposed taking into account the regio- and stereochemical outcome of the reaction.</p>}},
  author       = {{Diebler, J. and Spannenberg, A. and Werner, Thomas}},
  issn         = {{1477-0520}},
  journal      = {{Organic and Biomolecular Chemistry}},
  keywords     = {{CSSD}},
  number       = {{31}},
  pages        = {{7480--7489}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes}}},
  doi          = {{10.1039/c6ob01081d}},
  volume       = {{14}},
  year         = {{2016}},
}