[{"citation":{"chicago":"Schirmer, Marie-Luis, Anke Spannenberg, and Thomas Werner. “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.” <i>Acta Crystallographica Section C Structural Chemistry</i> 72, no. 6 (2016): 504–8. <a href=\"https://doi.org/10.1107/s2053229616008159\">https://doi.org/10.1107/s2053229616008159</a>.","short":"M.-L. Schirmer, A. Spannenberg, T. Werner, Acta Crystallographica Section C Structural Chemistry 72 (2016) 504–508.","apa":"Schirmer, M.-L., Spannenberg, A., &#38; Werner, T. (2016). 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. <i>Acta Crystallographica Section C Structural Chemistry</i>, <i>72</i>(6), 504–508. <a href=\"https://doi.org/10.1107/s2053229616008159\">https://doi.org/10.1107/s2053229616008159</a>","ieee":"M.-L. Schirmer, A. Spannenberg, and T. Werner, “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,” <i>Acta Crystallographica Section C Structural Chemistry</i>, vol. 72, no. 6, pp. 504–508, 2016, doi: <a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>.","ama":"Schirmer M-L, Spannenberg A, Werner T. 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. <i>Acta Crystallographica Section C Structural Chemistry</i>. 2016;72(6):504-508. doi:<a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>","bibtex":"@article{Schirmer_Spannenberg_Werner_2016, 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}, volume={72}, DOI={<a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>}, number={6}, journal={Acta Crystallographica Section C Structural Chemistry}, publisher={International Union of Crystallography (IUCr)}, author={Schirmer, Marie-Luis and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={504–508} }","mla":"Schirmer, Marie-Luis, et al. “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.” <i>Acta Crystallographica Section C Structural Chemistry</i>, vol. 72, no. 6, International Union of Crystallography (IUCr), 2016, pp. 504–08, doi:<a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>."},"status":"public","user_id":"89271","volume":72,"page":"504-508","publisher":"International Union of Crystallography (IUCr)","_id":"37984","abstract":[{"text":"<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>","lang":"eng"}],"extern":"1","issue":"6","publication":"Acta Crystallographica Section C Structural Chemistry","keyword":["T2"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T21:03:23Z","date_updated":"2025-11-10T09:23:46Z","publication_status":"published","intvolume":"        72","year":"2016","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","author":[{"full_name":"Schirmer, Marie-Luis","last_name":"Schirmer","first_name":"Marie-Luis"},{"full_name":"Spannenberg, Anke","last_name":"Spannenberg","first_name":"Anke"},{"id":"89271","full_name":"Werner, Thomas","last_name":"Werner","first_name":"Thomas","orcid":"0000-0001-9025-3244"}],"publication_identifier":{"issn":["2053-2296"]},"doi":"10.1107/s2053229616008159","language":[{"iso":"eng"}]},{"page":"7480-7489","_id":"37981","publisher":"Royal Society of Chemistry (RSC)","user_id":"89271","volume":14,"status":"public","citation":{"chicago":"Diebler, J., A. Spannenberg, and Thomas Werner. “Atom Economical Synthesis of Di- and Trithiocarbonates by the Lithium Tert-Butoxide Catalyzed Addition of Carbon Disulfide to Epoxides and Thiiranes.” <i>Organic and Biomolecular Chemistry</i> 14, no. 31 (2016): 7480–89. <a href=\"https://doi.org/10.1039/c6ob01081d\">https://doi.org/10.1039/c6ob01081d</a>.","short":"J. Diebler, A. Spannenberg, T. Werner, Organic and Biomolecular Chemistry 14 (2016) 7480–7489.","ieee":"J. Diebler, A. Spannenberg, and T. Werner, “Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes,” <i>Organic and Biomolecular Chemistry</i>, vol. 14, no. 31, pp. 7480–7489, 2016, doi: <a href=\"https://doi.org/10.1039/c6ob01081d\">10.1039/c6ob01081d</a>.","apa":"Diebler, J., Spannenberg, A., &#38; Werner, T. (2016). Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes. <i>Organic and Biomolecular Chemistry</i>, <i>14</i>(31), 7480–7489. <a href=\"https://doi.org/10.1039/c6ob01081d\">https://doi.org/10.1039/c6ob01081d</a>","bibtex":"@article{Diebler_Spannenberg_Werner_2016, title={Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes}, volume={14}, DOI={<a href=\"https://doi.org/10.1039/c6ob01081d\">10.1039/c6ob01081d</a>}, number={31}, journal={Organic and Biomolecular Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Diebler, J. and Spannenberg, A. and Werner, Thomas}, year={2016}, pages={7480–7489} }","ama":"Diebler J, Spannenberg A, Werner T. Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes. <i>Organic and Biomolecular Chemistry</i>. 2016;14(31):7480-7489. doi:<a href=\"https://doi.org/10.1039/c6ob01081d\">10.1039/c6ob01081d</a>","mla":"Diebler, J., et al. “Atom Economical Synthesis of Di- and Trithiocarbonates by the Lithium Tert-Butoxide Catalyzed Addition of Carbon Disulfide to Epoxides and Thiiranes.” <i>Organic and Biomolecular Chemistry</i>, vol. 14, no. 31, Royal Society of Chemistry (RSC), 2016, pp. 7480–89, doi:<a href=\"https://doi.org/10.1039/c6ob01081d\">10.1039/c6ob01081d</a>."},"language":[{"iso":"eng"}],"doi":"10.1039/c6ob01081d","year":"2016","title":"Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes","author":[{"full_name":"Diebler, J.","last_name":"Diebler","first_name":"J."},{"full_name":"Spannenberg, A.","first_name":"A.","last_name":"Spannenberg"},{"last_name":"Werner","first_name":"Thomas","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"publication_identifier":{"issn":["1477-0520","1477-0539"]},"date_updated":"2025-11-10T09:24:16Z","publication_status":"published","intvolume":"        14","date_created":"2023-01-22T21:01:59Z","type":"journal_article","keyword":["CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"publication":"Organic and Biomolecular Chemistry","issue":"31","abstract":[{"text":"<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>","lang":"eng"}],"extern":"1"},{"citation":{"mla":"Desens, Willi, et al. “A Novel Zinc Based Binary Catalytic System for CO<sub>2</sub>Utilization under Mild Conditions.” <i>Organic Chemistry Frontiers</i>, vol. 3, no. 2, Royal Society of Chemistry (RSC), 2016, pp. 156–64, doi:<a href=\"https://doi.org/10.1039/c5qo00356c\">10.1039/c5qo00356c</a>.","ama":"Desens W, Kohrt C, Spannenberg A, Werner T. A novel zinc based binary catalytic system for CO<sub>2</sub>utilization under mild conditions. <i>Organic Chemistry Frontiers</i>. 2016;3(2):156-164. doi:<a href=\"https://doi.org/10.1039/c5qo00356c\">10.1039/c5qo00356c</a>","bibtex":"@article{Desens_Kohrt_Spannenberg_Werner_2016, title={A novel zinc based binary catalytic system for CO<sub>2</sub>utilization under mild conditions}, volume={3}, DOI={<a href=\"https://doi.org/10.1039/c5qo00356c\">10.1039/c5qo00356c</a>}, number={2}, journal={Organic Chemistry Frontiers}, publisher={Royal Society of Chemistry (RSC)}, author={Desens, Willi and Kohrt, Christina and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={156–164} }","apa":"Desens, W., Kohrt, C., Spannenberg, A., &#38; Werner, T. (2016). A novel zinc based binary catalytic system for CO<sub>2</sub>utilization under mild conditions. <i>Organic Chemistry Frontiers</i>, <i>3</i>(2), 156–164. <a href=\"https://doi.org/10.1039/c5qo00356c\">https://doi.org/10.1039/c5qo00356c</a>","ieee":"W. Desens, C. Kohrt, A. Spannenberg, and T. Werner, “A novel zinc based binary catalytic system for CO<sub>2</sub>utilization under mild conditions,” <i>Organic Chemistry Frontiers</i>, vol. 3, no. 2, pp. 156–164, 2016, doi: <a href=\"https://doi.org/10.1039/c5qo00356c\">10.1039/c5qo00356c</a>.","short":"W. Desens, C. Kohrt, A. Spannenberg, T. Werner, Organic Chemistry Frontiers 3 (2016) 156–164.","chicago":"Desens, Willi, Christina Kohrt, Anke Spannenberg, and Thomas Werner. “A Novel Zinc Based Binary Catalytic System for CO<sub>2</sub>Utilization under Mild Conditions.” <i>Organic Chemistry Frontiers</i> 3, no. 2 (2016): 156–64. <a href=\"https://doi.org/10.1039/c5qo00356c\">https://doi.org/10.1039/c5qo00356c</a>."},"volume":3,"user_id":"89271","publisher":"Royal Society of Chemistry (RSC)","_id":"37987","page":"156-164","status":"public","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T1","T3","CSSD"],"type":"journal_article","date_created":"2023-01-22T21:04:30Z","extern":"1","abstract":[{"text":"<p>A novel zinc based binary catalytic system for the synthesis of cyclic carbonates under mild and solvent-free conditions utilizing CO<sub>2</sub>as a C1 building block is reported.</p>","lang":"eng"}],"publication":"Organic Chemistry Frontiers","issue":"2","doi":"10.1039/c5qo00356c","language":[{"iso":"eng"}],"intvolume":"         3","publication_status":"published","date_updated":"2025-11-10T09:26:28Z","author":[{"full_name":"Desens, Willi","first_name":"Willi","last_name":"Desens"},{"first_name":"Christina","last_name":"Kohrt","full_name":"Kohrt, Christina"},{"full_name":"Spannenberg, Anke","last_name":"Spannenberg","first_name":"Anke"},{"last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas","full_name":"Werner, Thomas","id":"89271"}],"publication_identifier":{"issn":["2052-4129"]},"year":"2016","title":"A novel zinc based binary catalytic system for CO<sub>2</sub>utilization under mild conditions"},{"citation":{"mla":"Diebler, Johannes, et al. “Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers.” <i>Macromolecules</i>, vol. 49, no. 13, American Chemical Society (ACS), 2016, pp. 4723–31, doi:<a href=\"https://doi.org/10.1021/acs.macromol.6b00728\">10.1021/acs.macromol.6b00728</a>.","ama":"Diebler J, Komber H, Häußler L, Lederer A, Werner T. Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers. <i>Macromolecules</i>. 2016;49(13):4723-4731. doi:<a href=\"https://doi.org/10.1021/acs.macromol.6b00728\">10.1021/acs.macromol.6b00728</a>","bibtex":"@article{Diebler_Komber_Häußler_Lederer_Werner_2016, title={Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers}, volume={49}, DOI={<a href=\"https://doi.org/10.1021/acs.macromol.6b00728\">10.1021/acs.macromol.6b00728</a>}, number={13}, journal={Macromolecules}, publisher={American Chemical Society (ACS)}, author={Diebler, Johannes and Komber, Hartmut and Häußler, Liane and Lederer, Albena and Werner, Thomas}, year={2016}, pages={4723–4731} }","apa":"Diebler, J., Komber, H., Häußler, L., Lederer, A., &#38; Werner, T. (2016). Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers. <i>Macromolecules</i>, <i>49</i>(13), 4723–4731. <a href=\"https://doi.org/10.1021/acs.macromol.6b00728\">https://doi.org/10.1021/acs.macromol.6b00728</a>","ieee":"J. Diebler, H. Komber, L. Häußler, A. Lederer, and T. Werner, “Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers,” <i>Macromolecules</i>, vol. 49, no. 13, pp. 4723–4731, 2016, doi: <a href=\"https://doi.org/10.1021/acs.macromol.6b00728\">10.1021/acs.macromol.6b00728</a>.","chicago":"Diebler, Johannes, Hartmut Komber, Liane Häußler, Albena Lederer, and Thomas Werner. “Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers.” <i>Macromolecules</i> 49, no. 13 (2016): 4723–31. <a href=\"https://doi.org/10.1021/acs.macromol.6b00728\">https://doi.org/10.1021/acs.macromol.6b00728</a>.","short":"J. Diebler, H. Komber, L. Häußler, A. Lederer, T. Werner, Macromolecules 49 (2016) 4723–4731."},"volume":49,"user_id":"89271","_id":"37982","publisher":"American Chemical Society (ACS)","page":"4723-4731","status":"public","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["CSSD"],"type":"journal_article","date_created":"2023-01-22T21:02:41Z","extern":"1","publication":"Macromolecules","issue":"13","doi":"10.1021/acs.macromol.6b00728","language":[{"iso":"eng"}],"intvolume":"        49","date_updated":"2025-11-10T09:25:16Z","publication_status":"published","author":[{"last_name":"Diebler","first_name":"Johannes","full_name":"Diebler, Johannes"},{"full_name":"Komber, Hartmut","first_name":"Hartmut","last_name":"Komber"},{"first_name":"Liane","last_name":"Häußler","full_name":"Häußler, Liane"},{"full_name":"Lederer, Albena","last_name":"Lederer","first_name":"Albena"},{"id":"89271","first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas"}],"publication_identifier":{"issn":["0024-9297","1520-5835"]},"year":"2016","title":"Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers"},{"intvolume":"         4","date_updated":"2025-11-10T09:26:56Z","publication_status":"published","author":[{"full_name":"Büttner, Hendrik","last_name":"Büttner","first_name":"Hendrik"},{"first_name":"Christoph","last_name":"Grimmer","full_name":"Grimmer, Christoph"},{"last_name":"Steinbauer","first_name":"Johannes","full_name":"Steinbauer, Johannes"},{"full_name":"Werner, Thomas","first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271"}],"publication_identifier":{"issn":["2168-0485","2168-0485"]},"title":"Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates","year":"2016","doi":"10.1021/acssuschemeng.6b01092","language":[{"iso":"eng"}],"extern":"1","issue":"9","publication":"ACS Sustainable Chemistry &amp; Engineering","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T1","T3","CSSD"],"type":"journal_article","date_created":"2023-01-22T21:01:04Z","status":"public","volume":4,"user_id":"89271","_id":"37980","publisher":"American Chemical Society (ACS)","page":"4805-4814","citation":{"short":"H. Büttner, C. Grimmer, J. Steinbauer, T. Werner, ACS Sustainable Chemistry &#38;amp; Engineering 4 (2016) 4805–4814.","ama":"Büttner H, Grimmer C, Steinbauer J, Werner T. Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates. <i>ACS Sustainable Chemistry &#38;amp; Engineering</i>. 2016;4(9):4805-4814. doi:<a href=\"https://doi.org/10.1021/acssuschemeng.6b01092\">10.1021/acssuschemeng.6b01092</a>","chicago":"Büttner, Hendrik, Christoph Grimmer, Johannes Steinbauer, and Thomas Werner. “Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates.” <i>ACS Sustainable Chemistry &#38;amp; Engineering</i> 4, no. 9 (2016): 4805–14. <a href=\"https://doi.org/10.1021/acssuschemeng.6b01092\">https://doi.org/10.1021/acssuschemeng.6b01092</a>.","bibtex":"@article{Büttner_Grimmer_Steinbauer_Werner_2016, title={Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates}, volume={4}, DOI={<a href=\"https://doi.org/10.1021/acssuschemeng.6b01092\">10.1021/acssuschemeng.6b01092</a>}, number={9}, journal={ACS Sustainable Chemistry &#38;amp; Engineering}, publisher={American Chemical Society (ACS)}, author={Büttner, Hendrik and Grimmer, Christoph and Steinbauer, Johannes and Werner, Thomas}, year={2016}, pages={4805–4814} }","mla":"Büttner, Hendrik, et al. “Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates.” <i>ACS Sustainable Chemistry &#38;amp; Engineering</i>, vol. 4, no. 9, American Chemical Society (ACS), 2016, pp. 4805–14, doi:<a href=\"https://doi.org/10.1021/acssuschemeng.6b01092\">10.1021/acssuschemeng.6b01092</a>.","apa":"Büttner, H., Grimmer, C., Steinbauer, J., &#38; Werner, T. (2016). Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates. <i>ACS Sustainable Chemistry &#38;amp; Engineering</i>, <i>4</i>(9), 4805–4814. <a href=\"https://doi.org/10.1021/acssuschemeng.6b01092\">https://doi.org/10.1021/acssuschemeng.6b01092</a>","ieee":"H. Büttner, C. Grimmer, J. Steinbauer, and T. Werner, “Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates,” <i>ACS Sustainable Chemistry &#38;amp; Engineering</i>, vol. 4, no. 9, pp. 4805–4814, 2016, doi: <a href=\"https://doi.org/10.1021/acssuschemeng.6b01092\">10.1021/acssuschemeng.6b01092</a>."}},{"citation":{"apa":"Schirmer, M.-L., Adomeit, S., Spannenberg, A., &#38; Werner, T. (2016). Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes. <i>Chemistry - A European Journal</i>, <i>22</i>(7), 2458–2465. <a href=\"https://doi.org/10.1002/chem.201503744\">https://doi.org/10.1002/chem.201503744</a>","ieee":"M.-L. Schirmer, S. Adomeit, A. Spannenberg, and T. Werner, “Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes,” <i>Chemistry - A European Journal</i>, vol. 22, no. 7, pp. 2458–2465, 2016, doi: <a href=\"https://doi.org/10.1002/chem.201503744\">10.1002/chem.201503744</a>.","short":"M.-L. Schirmer, S. Adomeit, A. Spannenberg, T. Werner, Chemistry - A European Journal 22 (2016) 2458–2465.","chicago":"Schirmer, Marie-Luis, Sven Adomeit, Anke Spannenberg, and Thomas Werner. “Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes.” <i>Chemistry - A European Journal</i> 22, no. 7 (2016): 2458–65. <a href=\"https://doi.org/10.1002/chem.201503744\">https://doi.org/10.1002/chem.201503744</a>.","mla":"Schirmer, Marie-Luis, et al. “Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes.” <i>Chemistry - A European Journal</i>, vol. 22, no. 7, Wiley, 2016, pp. 2458–65, doi:<a href=\"https://doi.org/10.1002/chem.201503744\">10.1002/chem.201503744</a>.","ama":"Schirmer M-L, Adomeit S, Spannenberg A, Werner T. Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes. <i>Chemistry - A European Journal</i>. 2016;22(7):2458-2465. doi:<a href=\"https://doi.org/10.1002/chem.201503744\">10.1002/chem.201503744</a>","bibtex":"@article{Schirmer_Adomeit_Spannenberg_Werner_2016, title={Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes}, volume={22}, DOI={<a href=\"https://doi.org/10.1002/chem.201503744\">10.1002/chem.201503744</a>}, number={7}, journal={Chemistry - A European Journal}, publisher={Wiley}, author={Schirmer, Marie-Luis and Adomeit, Sven and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={2458–2465} }"},"volume":22,"user_id":"89271","publisher":"Wiley","_id":"37986","page":"2458-2465","status":"public","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T2","CSSD"],"date_created":"2023-01-22T21:04:06Z","extern":"1","publication":"Chemistry - A European Journal","issue":"7","doi":"10.1002/chem.201503744","language":[{"iso":"eng"}],"intvolume":"        22","publication_status":"published","date_updated":"2025-11-10T09:23:00Z","publication_identifier":{"issn":["0947-6539"]},"author":[{"last_name":"Schirmer","first_name":"Marie-Luis","full_name":"Schirmer, Marie-Luis"},{"first_name":"Sven","last_name":"Adomeit","full_name":"Adomeit, Sven"},{"first_name":"Anke","last_name":"Spannenberg","full_name":"Spannenberg, Anke"},{"orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"title":"Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes","year":"2016"},{"citation":{"mla":"Diebler, Johannes, et al. “Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions.” <i>ChemCatChem</i>, vol. 8, no. 12, Wiley, 2016, pp. 2027–30, doi:<a href=\"https://doi.org/10.1002/cctc.201600242\">10.1002/cctc.201600242</a>.","ama":"Diebler J, Spannenberg A, Werner T. Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions. <i>ChemCatChem</i>. 2016;8(12):2027-2030. doi:<a href=\"https://doi.org/10.1002/cctc.201600242\">10.1002/cctc.201600242</a>","bibtex":"@article{Diebler_Spannenberg_Werner_2016, title={Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions}, volume={8}, DOI={<a href=\"https://doi.org/10.1002/cctc.201600242\">10.1002/cctc.201600242</a>}, number={12}, journal={ChemCatChem}, publisher={Wiley}, author={Diebler, Johannes and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={2027–2030} }","apa":"Diebler, J., Spannenberg, A., &#38; Werner, T. (2016). Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions. <i>ChemCatChem</i>, <i>8</i>(12), 2027–2030. <a href=\"https://doi.org/10.1002/cctc.201600242\">https://doi.org/10.1002/cctc.201600242</a>","ieee":"J. Diebler, A. Spannenberg, and T. Werner, “Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions,” <i>ChemCatChem</i>, vol. 8, no. 12, pp. 2027–2030, 2016, doi: <a href=\"https://doi.org/10.1002/cctc.201600242\">10.1002/cctc.201600242</a>.","short":"J. Diebler, A. Spannenberg, T. Werner, ChemCatChem 8 (2016) 2027–2030.","chicago":"Diebler, Johannes, Anke Spannenberg, and Thomas Werner. “Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions.” <i>ChemCatChem</i> 8, no. 12 (2016): 2027–30. <a href=\"https://doi.org/10.1002/cctc.201600242\">https://doi.org/10.1002/cctc.201600242</a>."},"user_id":"89271","volume":8,"page":"2027-2030","publisher":"Wiley","_id":"37985","status":"public","type":"journal_article","keyword":["CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T21:03:46Z","extern":"1","issue":"12","publication":"ChemCatChem","doi":"10.1002/cctc.201600242","language":[{"iso":"eng"}],"date_updated":"2025-11-10T09:24:45Z","publication_status":"published","intvolume":"         8","title":"Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions","year":"2016","author":[{"full_name":"Diebler, Johannes","first_name":"Johannes","last_name":"Diebler"},{"last_name":"Spannenberg","first_name":"Anke","full_name":"Spannenberg, Anke"},{"full_name":"Werner, Thomas","first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271"}],"publication_identifier":{"issn":["1867-3880"]}},{"status":"public","user_id":"89271","volume":358,"page":"622-630","publisher":"Wiley","_id":"37988","citation":{"mla":"Desens, Willi, and Thomas Werner. “Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates.” <i>Advanced Synthesis and Catalysis</i>, vol. 358, no. 4, Wiley, 2016, pp. 622–30, doi:<a href=\"https://doi.org/10.1002/adsc.201500941\">10.1002/adsc.201500941</a>.","bibtex":"@article{Desens_Werner_2016, title={Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates}, volume={358}, DOI={<a href=\"https://doi.org/10.1002/adsc.201500941\">10.1002/adsc.201500941</a>}, number={4}, journal={Advanced Synthesis and Catalysis}, publisher={Wiley}, author={Desens, Willi and Werner, Thomas}, year={2016}, pages={622–630} }","ama":"Desens W, Werner T. Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates. <i>Advanced Synthesis and Catalysis</i>. 2016;358(4):622-630. doi:<a href=\"https://doi.org/10.1002/adsc.201500941\">10.1002/adsc.201500941</a>","ieee":"W. Desens and T. Werner, “Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates,” <i>Advanced Synthesis and Catalysis</i>, vol. 358, no. 4, pp. 622–630, 2016, doi: <a href=\"https://doi.org/10.1002/adsc.201500941\">10.1002/adsc.201500941</a>.","apa":"Desens, W., &#38; Werner, T. (2016). Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates. <i>Advanced Synthesis and Catalysis</i>, <i>358</i>(4), 622–630. <a href=\"https://doi.org/10.1002/adsc.201500941\">https://doi.org/10.1002/adsc.201500941</a>","chicago":"Desens, Willi, and Thomas Werner. “Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates.” <i>Advanced Synthesis and Catalysis</i> 358, no. 4 (2016): 622–30. <a href=\"https://doi.org/10.1002/adsc.201500941\">https://doi.org/10.1002/adsc.201500941</a>.","short":"W. Desens, T. Werner, Advanced Synthesis and Catalysis 358 (2016) 622–630."},"date_updated":"2025-11-10T09:25:53Z","publication_status":"published","intvolume":"       358","year":"2016","title":"Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates","author":[{"full_name":"Desens, Willi","first_name":"Willi","last_name":"Desens"},{"id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"publication_identifier":{"issn":["1615-4150"]},"doi":"10.1002/adsc.201500941","language":[{"iso":"eng"}],"extern":"1","issue":"4","publication":"Advanced Synthesis and Catalysis","keyword":["T1","CSSD"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T21:04:52Z"},{"volume":2015,"user_id":"89271","publisher":"Wiley","_id":"37996","page":"3286-3295","status":"public","citation":{"apa":"Werner, T., Hoffmann, M., &#38; Deshmukh, S. (2015). Phospholane-Catalyzed Wittig Reaction. <i>European Journal of Organic Chemistry</i>, <i>2015</i>(15), 3286–3295. <a href=\"https://doi.org/10.1002/ejoc.201500243\">https://doi.org/10.1002/ejoc.201500243</a>","ieee":"T. Werner, M. Hoffmann, and S. Deshmukh, “Phospholane-Catalyzed Wittig Reaction,” <i>European Journal of Organic Chemistry</i>, vol. 2015, no. 15, pp. 3286–3295, 2015, doi: <a href=\"https://doi.org/10.1002/ejoc.201500243\">10.1002/ejoc.201500243</a>.","short":"T. Werner, M. Hoffmann, S. Deshmukh, European Journal of Organic Chemistry 2015 (2015) 3286–3295.","chicago":"Werner, Thomas, Marcel Hoffmann, and Sunetra Deshmukh. “Phospholane-Catalyzed Wittig Reaction.” <i>European Journal of Organic Chemistry</i> 2015, no. 15 (2015): 3286–95. <a href=\"https://doi.org/10.1002/ejoc.201500243\">https://doi.org/10.1002/ejoc.201500243</a>.","mla":"Werner, Thomas, et al. “Phospholane-Catalyzed Wittig Reaction.” <i>European Journal of Organic Chemistry</i>, vol. 2015, no. 15, Wiley, 2015, pp. 3286–95, doi:<a href=\"https://doi.org/10.1002/ejoc.201500243\">10.1002/ejoc.201500243</a>.","ama":"Werner T, Hoffmann M, Deshmukh S. Phospholane-Catalyzed Wittig Reaction. <i>European Journal of Organic Chemistry</i>. 2015;2015(15):3286-3295. doi:<a href=\"https://doi.org/10.1002/ejoc.201500243\">10.1002/ejoc.201500243</a>","bibtex":"@article{Werner_Hoffmann_Deshmukh_2015, title={Phospholane-Catalyzed Wittig Reaction}, volume={2015}, DOI={<a href=\"https://doi.org/10.1002/ejoc.201500243\">10.1002/ejoc.201500243</a>}, number={15}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Werner, Thomas and Hoffmann, Marcel and Deshmukh, Sunetra}, year={2015}, pages={3286–3295} }"},"alternative_title":["Phospholane-Catalyzed Wittig Reaction"],"doi":"10.1002/ejoc.201500243","language":[{"iso":"eng"}],"intvolume":"      2015","date_updated":"2025-11-10T09:27:56Z","publication_status":"published","publication_identifier":{"issn":["1434-193X"]},"author":[{"full_name":"Werner, Thomas","last_name":"Werner","first_name":"Thomas","orcid":"0000-0001-9025-3244","id":"89271"},{"full_name":"Hoffmann, Marcel","last_name":"Hoffmann","first_name":"Marcel"},{"last_name":"Deshmukh","first_name":"Sunetra","full_name":"Deshmukh, Sunetra"}],"year":"2015","title":"Phospholane-Catalyzed Wittig Reaction","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2","CSSD"],"type":"journal_article","date_created":"2023-01-22T21:07:48Z","extern":"1","issue":"15","publication":"European Journal of Organic Chemistry"},{"language":[{"iso":"eng"}],"doi":"10.1107/s2056989015019313","publication_identifier":{"issn":["2056-9890"]},"author":[{"last_name":"Schirmer","first_name":"Marie-Luis","full_name":"Schirmer, Marie-Luis"},{"last_name":"Spannenberg","first_name":"Anke","full_name":"Spannenberg, Anke"},{"id":"89271","full_name":"Werner, Thomas","first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"title":"Crystal structure of diethyl (<i>E</i>)-2-[(benzofuran-2-yl)methylidene]succinate","year":"2015","intvolume":"        71","date_updated":"2025-11-10T09:28:18Z","publication_status":"published","date_created":"2023-01-22T21:06:01Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T2"],"issue":"11","publication":"Acta Crystallographica Section E Crystallographic Communications","abstract":[{"lang":"eng","text":"<jats:p>The title compound, C<jats:sub>17</jats:sub>H<jats:sub>18</jats:sub>O<jats:sub>5</jats:sub>, was synthesized by a base-free catalytic Wittig reaction. The molecule consists of a diethyl itaconate unit, which is connected<jats:italic>via</jats:italic>the C=C double bond to a benzofuran moiety. The benzofuran ring system (r.m.s. deviation = 0.007 Å) forms dihedral angles of 79.58 (4) and 12.12 (10)° with the mean planes through the<jats:italic>cis</jats:italic>and<jats:italic>trans</jats:italic>ethoxycarbonyl groups, respectively. An intramolecular C—H...O hydrogen bond involving the O atom of the benzofuran moiety is observed. In the crystal, molecules are linked into ribbons running parallel to the<jats:italic>b</jats:italic>axis by C—H...O hydrogen bonds.</jats:p>"}],"extern":"1","publisher":"International Union of Crystallography (IUCr)","_id":"37991","page":"o872-o872","volume":71,"user_id":"89271","status":"public","citation":{"apa":"Schirmer, M.-L., Spannenberg, A., &#38; Werner, T. (2015). Crystal structure of diethyl (<i>E</i>)-2-[(benzofuran-2-yl)methylidene]succinate. <i>Acta Crystallographica Section E Crystallographic Communications</i>, <i>71</i>(11), o872–o872. <a href=\"https://doi.org/10.1107/s2056989015019313\">https://doi.org/10.1107/s2056989015019313</a>","ieee":"M.-L. Schirmer, A. Spannenberg, and T. Werner, “Crystal structure of diethyl (<i>E</i>)-2-[(benzofuran-2-yl)methylidene]succinate,” <i>Acta Crystallographica Section E Crystallographic Communications</i>, vol. 71, no. 11, pp. o872–o872, 2015, doi: <a href=\"https://doi.org/10.1107/s2056989015019313\">10.1107/s2056989015019313</a>.","short":"M.-L. Schirmer, A. Spannenberg, T. Werner, Acta Crystallographica Section E Crystallographic Communications 71 (2015) o872–o872.","chicago":"Schirmer, Marie-Luis, Anke Spannenberg, and Thomas Werner. “Crystal Structure of Diethyl (<i>E</i>)-2-[(Benzofuran-2-Yl)Methylidene]Succinate.” <i>Acta Crystallographica Section E Crystallographic Communications</i> 71, no. 11 (2015): o872–o872. <a href=\"https://doi.org/10.1107/s2056989015019313\">https://doi.org/10.1107/s2056989015019313</a>.","mla":"Schirmer, Marie-Luis, et al. “Crystal Structure of Diethyl (<i>E</i>)-2-[(Benzofuran-2-Yl)Methylidene]Succinate.” <i>Acta Crystallographica Section E Crystallographic Communications</i>, vol. 71, no. 11, International Union of Crystallography (IUCr), 2015, pp. o872–o872, doi:<a href=\"https://doi.org/10.1107/s2056989015019313\">10.1107/s2056989015019313</a>.","ama":"Schirmer M-L, Spannenberg A, Werner T. Crystal structure of diethyl (<i>E</i>)-2-[(benzofuran-2-yl)methylidene]succinate. <i>Acta Crystallographica Section E Crystallographic Communications</i>. 2015;71(11):o872-o872. doi:<a href=\"https://doi.org/10.1107/s2056989015019313\">10.1107/s2056989015019313</a>","bibtex":"@article{Schirmer_Spannenberg_Werner_2015, title={Crystal structure of diethyl (<i>E</i>)-2-[(benzofuran-2-yl)methylidene]succinate}, volume={71}, DOI={<a href=\"https://doi.org/10.1107/s2056989015019313\">10.1107/s2056989015019313</a>}, number={11}, journal={Acta Crystallographica Section E Crystallographic Communications}, publisher={International Union of Crystallography (IUCr)}, author={Schirmer, Marie-Luis and Spannenberg, Anke and Werner, Thomas}, year={2015}, pages={o872–o872} }"}},{"extern":"1","issue":"20","publication":"European Journal of Organic Chemistry","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T2","CSSD"],"date_created":"2023-01-22T21:07:09Z","intvolume":"      2015","date_updated":"2025-11-10T09:29:30Z","publication_status":"published","publication_identifier":{"issn":["1434-193X"]},"author":[{"full_name":"Hoffmann, Marcel","last_name":"Hoffmann","first_name":"Marcel"},{"first_name":"Sunetra","last_name":"Deshmukh","full_name":"Deshmukh, Sunetra"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"year":"2015","title":"Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction","alternative_title":["The Microwave-Assisted Catalytic Wittig Reaction"],"doi":"10.1002/ejoc.201500310","language":[{"iso":"eng"}],"citation":{"ama":"Hoffmann M, Deshmukh S, Werner T. Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction. <i>European Journal of Organic Chemistry</i>. 2015;2015(20):4532-4543. doi:<a href=\"https://doi.org/10.1002/ejoc.201500310\">10.1002/ejoc.201500310</a>","bibtex":"@article{Hoffmann_Deshmukh_Werner_2015, title={Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction}, volume={2015}, DOI={<a href=\"https://doi.org/10.1002/ejoc.201500310\">10.1002/ejoc.201500310</a>}, number={20}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Hoffmann, Marcel and Deshmukh, Sunetra and Werner, Thomas}, year={2015}, pages={4532–4543} }","mla":"Hoffmann, Marcel, et al. “Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction.” <i>European Journal of Organic Chemistry</i>, vol. 2015, no. 20, Wiley, 2015, pp. 4532–43, doi:<a href=\"https://doi.org/10.1002/ejoc.201500310\">10.1002/ejoc.201500310</a>.","short":"M. Hoffmann, S. Deshmukh, T. Werner, European Journal of Organic Chemistry 2015 (2015) 4532–4543.","chicago":"Hoffmann, Marcel, Sunetra Deshmukh, and Thomas Werner. “Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction.” <i>European Journal of Organic Chemistry</i> 2015, no. 20 (2015): 4532–43. <a href=\"https://doi.org/10.1002/ejoc.201500310\">https://doi.org/10.1002/ejoc.201500310</a>.","apa":"Hoffmann, M., Deshmukh, S., &#38; Werner, T. (2015). Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction. <i>European Journal of Organic Chemistry</i>, <i>2015</i>(20), 4532–4543. <a href=\"https://doi.org/10.1002/ejoc.201500310\">https://doi.org/10.1002/ejoc.201500310</a>","ieee":"M. Hoffmann, S. Deshmukh, and T. Werner, “Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction,” <i>European Journal of Organic Chemistry</i>, vol. 2015, no. 20, pp. 4532–4543, 2015, doi: <a href=\"https://doi.org/10.1002/ejoc.201500310\">10.1002/ejoc.201500310</a>."},"status":"public","volume":2015,"user_id":"89271","publisher":"Wiley","_id":"37994","page":"4532-4543"},{"publication":"ACS Sustainable Chemistry and Engineering","issue":"11","extern":"1","date_created":"2023-01-22T21:06:26Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T1","T2","CSSD"],"publication_identifier":{"issn":["2168-0485","2168-0485"]},"author":[{"full_name":"Großeheilmann, Julia","first_name":"Julia","last_name":"Großeheilmann"},{"last_name":"Büttner","first_name":"Hendrik","full_name":"Büttner, Hendrik"},{"full_name":"Kohrt, Christina","last_name":"Kohrt","first_name":"Christina"},{"full_name":"Kragl, Udo","last_name":"Kragl","first_name":"Udo"},{"full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas","id":"89271"}],"title":"Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration","year":"2015","intvolume":"         3","date_updated":"2025-11-10T09:30:37Z","publication_status":"published","language":[{"iso":"eng"}],"doi":"10.1021/acssuschemeng.5b00734","citation":{"mla":"Großeheilmann, Julia, et al. “Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration.” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 3, no. 11, American Chemical Society (ACS), 2015, pp. 2817–22, doi:<a href=\"https://doi.org/10.1021/acssuschemeng.5b00734\">10.1021/acssuschemeng.5b00734</a>.","ama":"Großeheilmann J, Büttner H, Kohrt C, Kragl U, Werner T. Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration. <i>ACS Sustainable Chemistry and Engineering</i>. 2015;3(11):2817-2822. doi:<a href=\"https://doi.org/10.1021/acssuschemeng.5b00734\">10.1021/acssuschemeng.5b00734</a>","bibtex":"@article{Großeheilmann_Büttner_Kohrt_Kragl_Werner_2015, title={Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration}, volume={3}, DOI={<a href=\"https://doi.org/10.1021/acssuschemeng.5b00734\">10.1021/acssuschemeng.5b00734</a>}, number={11}, journal={ACS Sustainable Chemistry and Engineering}, publisher={American Chemical Society (ACS)}, author={Großeheilmann, Julia and Büttner, Hendrik and Kohrt, Christina and Kragl, Udo and Werner, Thomas}, year={2015}, pages={2817–2822} }","apa":"Großeheilmann, J., Büttner, H., Kohrt, C., Kragl, U., &#38; Werner, T. (2015). Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration. <i>ACS Sustainable Chemistry and Engineering</i>, <i>3</i>(11), 2817–2822. <a href=\"https://doi.org/10.1021/acssuschemeng.5b00734\">https://doi.org/10.1021/acssuschemeng.5b00734</a>","ieee":"J. Großeheilmann, H. Büttner, C. Kohrt, U. Kragl, and T. Werner, “Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration,” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 3, no. 11, pp. 2817–2822, 2015, doi: <a href=\"https://doi.org/10.1021/acssuschemeng.5b00734\">10.1021/acssuschemeng.5b00734</a>.","chicago":"Großeheilmann, Julia, Hendrik Büttner, Christina Kohrt, Udo Kragl, and Thomas Werner. “Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration.” <i>ACS Sustainable Chemistry and Engineering</i> 3, no. 11 (2015): 2817–22. <a href=\"https://doi.org/10.1021/acssuschemeng.5b00734\">https://doi.org/10.1021/acssuschemeng.5b00734</a>.","short":"J. Großeheilmann, H. Büttner, C. Kohrt, U. Kragl, T. Werner, ACS Sustainable Chemistry and Engineering 3 (2015) 2817–2822."},"status":"public","publisher":"American Chemical Society (ACS)","_id":"37992","page":"2817-2822","volume":3,"user_id":"89271"},{"volume":8,"user_id":"89271","publisher":"Wiley","_id":"37993","page":"2655-2669","status":"public","citation":{"bibtex":"@article{Büttner_Steinbauer_Werner_2015, title={Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts}, volume={8}, DOI={<a href=\"https://doi.org/10.1002/cssc.201500612\">10.1002/cssc.201500612</a>}, number={16}, journal={ChemSusChem}, publisher={Wiley}, author={Büttner, Hendrik and Steinbauer, Johannes and Werner, Thomas}, year={2015}, pages={2655–2669} }","ama":"Büttner H, Steinbauer J, Werner T. 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Deshmukh, European Journal of Organic Chemistry 2014 (2014) 6873–6876.","chicago":"Werner, Thomas, Marcel Hoffmann, and Sunetra Deshmukh. “First Microwave-Assisted Catalytic Wittig Reaction.” <i>European Journal of Organic Chemistry</i> 2014, no. 31 (2014): 6873–76. <a href=\"https://doi.org/10.1002/ejoc.201403113\">https://doi.org/10.1002/ejoc.201403113</a>.","apa":"Werner, T., Hoffmann, M., &#38; Deshmukh, S. (2014). First Microwave-Assisted Catalytic Wittig Reaction. <i>European Journal of Organic Chemistry</i>, <i>2014</i>(31), 6873–6876. <a href=\"https://doi.org/10.1002/ejoc.201403113\">https://doi.org/10.1002/ejoc.201403113</a>","ieee":"T. Werner, M. Hoffmann, and S. Deshmukh, “First Microwave-Assisted Catalytic Wittig Reaction,” <i>European Journal of Organic Chemistry</i>, vol. 2014, no. 31, pp. 6873–6876, 2014, doi: <a href=\"https://doi.org/10.1002/ejoc.201403113\">10.1002/ejoc.201403113</a>."}}]