[{"type":"journal_article","status":"public","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37981","extern":"1","publication_status":"published","publication_identifier":{"issn":["1477-0520","1477-0539"]},"citation":{"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>","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>.","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.","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>.","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} }","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>"},"intvolume":"        14","page":"7480-7489","author":[{"first_name":"J.","full_name":"Diebler, J.","last_name":"Diebler"},{"first_name":"A.","full_name":"Spannenberg, A.","last_name":"Spannenberg"},{"last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271","first_name":"Thomas"}],"volume":14,"date_updated":"2025-11-10T09:24:16Z","doi":"10.1039/c6ob01081d","publication":"Organic and Biomolecular Chemistry","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"}],"language":[{"iso":"eng"}],"keyword":["CSSD"],"issue":"31","year":"2016","date_created":"2023-01-22T21:01:59Z","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"},{"date_created":"2023-01-22T21:04:30Z","publisher":"Royal Society of Chemistry (RSC)","title":"A novel zinc based binary catalytic system for CO<sub>2</sub>utilization under mild conditions","issue":"2","year":"2016","language":[{"iso":"eng"}],"keyword":["T1","T3","CSSD"],"publication":"Organic Chemistry Frontiers","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"}],"volume":3,"author":[{"full_name":"Desens, Willi","last_name":"Desens","first_name":"Willi"},{"full_name":"Kohrt, Christina","last_name":"Kohrt","first_name":"Christina"},{"last_name":"Spannenberg","full_name":"Spannenberg, Anke","first_name":"Anke"},{"full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"date_updated":"2025-11-10T09:26:28Z","doi":"10.1039/c5qo00356c","publication_identifier":{"issn":["2052-4129"]},"publication_status":"published","intvolume":"         3","page":"156-164","citation":{"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>","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>.","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>.","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} }","short":"W. Desens, C. Kohrt, A. Spannenberg, T. Werner, Organic Chemistry Frontiers 3 (2016) 156–164.","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>.","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>"},"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37987","extern":"1","type":"journal_article","status":"public"},{"status":"public","type":"journal_article","extern":"1","_id":"37982","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"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>.","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} }","short":"J. Diebler, H. Komber, L. Häußler, A. Lederer, T. Werner, Macromolecules 49 (2016) 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>","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>","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>.","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>."},"intvolume":"        49","page":"4723-4731","publication_status":"published","publication_identifier":{"issn":["0024-9297","1520-5835"]},"doi":"10.1021/acs.macromol.6b00728","date_updated":"2025-11-10T09:25:16Z","author":[{"last_name":"Diebler","full_name":"Diebler, Johannes","first_name":"Johannes"},{"full_name":"Komber, Hartmut","last_name":"Komber","first_name":"Hartmut"},{"first_name":"Liane","last_name":"Häußler","full_name":"Häußler, Liane"},{"first_name":"Albena","full_name":"Lederer, Albena","last_name":"Lederer"},{"full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"volume":49,"publication":"Macromolecules","keyword":["CSSD"],"language":[{"iso":"eng"}],"year":"2016","issue":"13","title":"Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers","publisher":"American Chemical Society (ACS)","date_created":"2023-01-22T21:02:41Z"},{"keyword":["T1","T3","CSSD"],"language":[{"iso":"eng"}],"publication":"ACS Sustainable Chemistry &amp; Engineering","publisher":"American Chemical Society (ACS)","date_created":"2023-01-22T21:01:04Z","title":"Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates","issue":"9","year":"2016","_id":"37980","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","extern":"1","type":"journal_article","status":"public","date_updated":"2025-11-10T09:26:56Z","volume":4,"author":[{"full_name":"Büttner, Hendrik","last_name":"Büttner","first_name":"Hendrik"},{"last_name":"Grimmer","full_name":"Grimmer, Christoph","first_name":"Christoph"},{"full_name":"Steinbauer, Johannes","last_name":"Steinbauer","first_name":"Johannes"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner"}],"doi":"10.1021/acssuschemeng.6b01092","publication_identifier":{"issn":["2168-0485","2168-0485"]},"publication_status":"published","page":"4805-4814","intvolume":"         4","citation":{"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>.","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>.","short":"H. Büttner, C. Grimmer, J. Steinbauer, T. Werner, ACS Sustainable Chemistry &#38;amp; Engineering 4 (2016) 4805–4814.","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>"}},{"publication_status":"published","publication_identifier":{"issn":["0947-6539"]},"issue":"7","year":"2016","citation":{"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>.","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>.","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>","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>","short":"M.-L. Schirmer, S. Adomeit, A. Spannenberg, T. Werner, Chemistry - A European Journal 22 (2016) 2458–2465.","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} }","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>."},"intvolume":"        22","page":"2458-2465","publisher":"Wiley","date_updated":"2025-11-10T09:23:00Z","date_created":"2023-01-22T21:04:06Z","author":[{"last_name":"Schirmer","full_name":"Schirmer, Marie-Luis","first_name":"Marie-Luis"},{"last_name":"Adomeit","full_name":"Adomeit, Sven","first_name":"Sven"},{"last_name":"Spannenberg","full_name":"Spannenberg, Anke","first_name":"Anke"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"volume":22,"title":"Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes","doi":"10.1002/chem.201503744","type":"journal_article","publication":"Chemistry - A European Journal","status":"public","_id":"37986","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2","CSSD"],"language":[{"iso":"eng"}],"extern":"1"},{"publication_identifier":{"issn":["1867-3880"]},"publication_status":"published","page":"2027-2030","intvolume":"         8","citation":{"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>","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} }","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>.","short":"J. Diebler, A. Spannenberg, T. Werner, ChemCatChem 8 (2016) 2027–2030.","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>","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>.","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>."},"date_updated":"2025-11-10T09:24:45Z","volume":8,"author":[{"last_name":"Diebler","full_name":"Diebler, Johannes","first_name":"Johannes"},{"last_name":"Spannenberg","full_name":"Spannenberg, Anke","first_name":"Anke"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas"}],"doi":"10.1002/cctc.201600242","type":"journal_article","status":"public","_id":"37985","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","extern":"1","issue":"12","year":"2016","publisher":"Wiley","date_created":"2023-01-22T21:03:46Z","title":"Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions","publication":"ChemCatChem","keyword":["CSSD"],"language":[{"iso":"eng"}]},{"issue":"4","publication_status":"published","publication_identifier":{"issn":["1615-4150"]},"citation":{"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>.","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>.","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>","short":"W. Desens, T. Werner, Advanced Synthesis and Catalysis 358 (2016) 622–630.","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} }","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>."},"intvolume":"       358","page":"622-630","year":"2016","date_created":"2023-01-22T21:04:52Z","author":[{"full_name":"Desens, Willi","last_name":"Desens","first_name":"Willi"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas"}],"volume":358,"date_updated":"2025-11-10T09:25:53Z","publisher":"Wiley","doi":"10.1002/adsc.201500941","title":"Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates","type":"journal_article","publication":"Advanced Synthesis and Catalysis","status":"public","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37988","extern":"1","language":[{"iso":"eng"}],"keyword":["T1","CSSD"]},{"citation":{"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>.","short":"T. Werner, M. Hoffmann, S. Deshmukh, European Journal of Organic Chemistry 2015 (2015) 3286–3295.","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} }","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>.","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>.","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>"},"intvolume":"      2015","page":"3286-3295","year":"2015","issue":"15","publication_status":"published","publication_identifier":{"issn":["1434-193X"]},"doi":"10.1002/ejoc.201500243","title":"Phospholane-Catalyzed Wittig Reaction","date_created":"2023-01-22T21:07:48Z","author":[{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"},{"last_name":"Hoffmann","full_name":"Hoffmann, Marcel","first_name":"Marcel"},{"full_name":"Deshmukh, Sunetra","last_name":"Deshmukh","first_name":"Sunetra"}],"volume":2015,"date_updated":"2025-11-10T09:27:56Z","publisher":"Wiley","status":"public","type":"journal_article","publication":"European Journal of Organic Chemistry","alternative_title":["Phospholane-Catalyzed Wittig Reaction"],"language":[{"iso":"eng"}],"extern":"1","keyword":["T2","CSSD"],"user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37996"},{"user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37991","extern":"1","type":"journal_article","status":"public","author":[{"first_name":"Marie-Luis","last_name":"Schirmer","full_name":"Schirmer, Marie-Luis"},{"first_name":"Anke","full_name":"Spannenberg, Anke","last_name":"Spannenberg"},{"full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"volume":71,"date_updated":"2025-11-10T09:28:18Z","doi":"10.1107/s2056989015019313","publication_status":"published","publication_identifier":{"issn":["2056-9890"]},"citation":{"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>","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>.","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>.","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>","short":"M.-L. Schirmer, A. Spannenberg, T. Werner, Acta Crystallographica Section E Crystallographic Communications 71 (2015) o872–o872.","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} }","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>."},"intvolume":"        71","page":"o872-o872","language":[{"iso":"eng"}],"keyword":["T2"],"publication":"Acta Crystallographica Section E Crystallographic Communications","abstract":[{"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>","lang":"eng"}],"date_created":"2023-01-22T21:06:01Z","publisher":"International Union of Crystallography (IUCr)","title":"Crystal structure of diethyl (<i>E</i>)-2-[(benzofuran-2-yl)methylidene]succinate","issue":"11","year":"2015"},{"keyword":["T2","CSSD"],"alternative_title":["The Microwave-Assisted Catalytic Wittig Reaction"],"extern":"1","language":[{"iso":"eng"}],"_id":"37994","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"status":"public","type":"journal_article","publication":"European Journal of Organic Chemistry","title":"Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction","doi":"10.1002/ejoc.201500310","publisher":"Wiley","date_updated":"2025-11-10T09:29:30Z","author":[{"first_name":"Marcel","full_name":"Hoffmann, Marcel","last_name":"Hoffmann"},{"first_name":"Sunetra","last_name":"Deshmukh","full_name":"Deshmukh, Sunetra"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner"}],"date_created":"2023-01-22T21:07:09Z","volume":2015,"year":"2015","citation":{"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>","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.","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>.","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>.","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>"},"page":"4532-4543","intvolume":"      2015","publication_status":"published","publication_identifier":{"issn":["1434-193X"]},"issue":"20"},{"year":"2015","issue":"11","title":"Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration","date_created":"2023-01-22T21:06:26Z","publisher":"American Chemical Society (ACS)","publication":"ACS Sustainable Chemistry and Engineering","language":[{"iso":"eng"}],"keyword":["T1","T2","CSSD"],"citation":{"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>","short":"J. Großeheilmann, H. Büttner, C. Kohrt, U. Kragl, T. Werner, ACS Sustainable Chemistry and Engineering 3 (2015) 2817–2822.","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} }","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>.","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>.","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>.","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>"},"page":"2817-2822","intvolume":"         3","publication_status":"published","publication_identifier":{"issn":["2168-0485","2168-0485"]},"doi":"10.1021/acssuschemeng.5b00734","author":[{"full_name":"Großeheilmann, Julia","last_name":"Großeheilmann","first_name":"Julia"},{"first_name":"Hendrik","last_name":"Büttner","full_name":"Büttner, Hendrik"},{"first_name":"Christina","last_name":"Kohrt","full_name":"Kohrt, Christina"},{"last_name":"Kragl","full_name":"Kragl, Udo","first_name":"Udo"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"volume":3,"date_updated":"2025-11-10T09:30:37Z","status":"public","type":"journal_article","extern":"1","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37992"},{"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37993","extern":"1","type":"journal_article","status":"public","volume":8,"author":[{"full_name":"Büttner, Hendrik","last_name":"Büttner","first_name":"Hendrik"},{"first_name":"Johannes","last_name":"Steinbauer","full_name":"Steinbauer, Johannes"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271","full_name":"Werner, Thomas"}],"date_updated":"2025-11-10T09:31:34Z","doi":"10.1002/cssc.201500612","publication_identifier":{"issn":["1864-5631"]},"publication_status":"published","page":"2655-2669","intvolume":"         8","citation":{"mla":"Büttner, Hendrik, et al. “Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts.” <i>ChemSusChem</i>, vol. 8, no. 16, Wiley, 2015, pp. 2655–69, doi:<a href=\"https://doi.org/10.1002/cssc.201500612\">10.1002/cssc.201500612</a>.","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} }","short":"H. Büttner, J. Steinbauer, T. Werner, ChemSusChem 8 (2015) 2655–2669.","apa":"Büttner, H., Steinbauer, J., &#38; Werner, T. (2015). Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts. <i>ChemSusChem</i>, <i>8</i>(16), 2655–2669. <a href=\"https://doi.org/10.1002/cssc.201500612\">https://doi.org/10.1002/cssc.201500612</a>","ama":"Büttner H, Steinbauer J, Werner T. Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts. <i>ChemSusChem</i>. 2015;8(16):2655-2669. doi:<a href=\"https://doi.org/10.1002/cssc.201500612\">10.1002/cssc.201500612</a>","ieee":"H. Büttner, J. Steinbauer, and T. Werner, “Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts,” <i>ChemSusChem</i>, vol. 8, no. 16, pp. 2655–2669, 2015, doi: <a href=\"https://doi.org/10.1002/cssc.201500612\">10.1002/cssc.201500612</a>.","chicago":"Büttner, Hendrik, Johannes Steinbauer, and Thomas Werner. “Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts.” <i>ChemSusChem</i> 8, no. 16 (2015): 2655–69. <a href=\"https://doi.org/10.1002/cssc.201500612\">https://doi.org/10.1002/cssc.201500612</a>."},"language":[{"iso":"eng"}],"keyword":["T1","T2","CSSD"],"publication":"ChemSusChem","date_created":"2023-01-22T21:06:51Z","publisher":"Wiley","title":"Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts","issue":"16","year":"2015"},{"doi":"10.1002/cssc.201500128","title":"Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides","date_created":"2023-01-22T21:08:10Z","author":[{"full_name":"Kohrt, Christina","last_name":"Kohrt","first_name":"Christina"},{"id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"volume":8,"publisher":"Wiley","date_updated":"2025-11-10T09:30:13Z","citation":{"ieee":"C. Kohrt and T. Werner, “Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides,” <i>ChemSusChem</i>, vol. 8, no. 12, pp. 2031–2034, 2015, doi: <a href=\"https://doi.org/10.1002/cssc.201500128\">10.1002/cssc.201500128</a>.","chicago":"Kohrt, Christina, and Thomas Werner. “Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides.” <i>ChemSusChem</i> 8, no. 12 (2015): 2031–34. <a href=\"https://doi.org/10.1002/cssc.201500128\">https://doi.org/10.1002/cssc.201500128</a>.","ama":"Kohrt C, Werner T. Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides. <i>ChemSusChem</i>. 2015;8(12):2031-2034. doi:<a href=\"https://doi.org/10.1002/cssc.201500128\">10.1002/cssc.201500128</a>","bibtex":"@article{Kohrt_Werner_2015, title={Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides}, volume={8}, DOI={<a href=\"https://doi.org/10.1002/cssc.201500128\">10.1002/cssc.201500128</a>}, number={12}, journal={ChemSusChem}, publisher={Wiley}, author={Kohrt, Christina and Werner, Thomas}, year={2015}, pages={2031–2034} }","short":"C. Kohrt, T. Werner, ChemSusChem 8 (2015) 2031–2034.","mla":"Kohrt, Christina, and Thomas Werner. “Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides.” <i>ChemSusChem</i>, vol. 8, no. 12, Wiley, 2015, pp. 2031–34, doi:<a href=\"https://doi.org/10.1002/cssc.201500128\">10.1002/cssc.201500128</a>.","apa":"Kohrt, C., &#38; Werner, T. (2015). Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides. <i>ChemSusChem</i>, <i>8</i>(12), 2031–2034. <a href=\"https://doi.org/10.1002/cssc.201500128\">https://doi.org/10.1002/cssc.201500128</a>"},"intvolume":"         8","page":"2031-2034","year":"2015","issue":"12","publication_status":"published","publication_identifier":{"issn":["1864-5631"]},"language":[{"iso":"eng"}],"extern":"1","keyword":["T1","T2","CSSD"],"user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37997","status":"public","type":"journal_article","publication":"ChemSusChem"},{"publication":"ChemSusChem","type":"journal_article","status":"public","_id":"37990","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","keyword":["T1","T2","CSSD"],"extern":"1","language":[{"iso":"eng"}],"publication_identifier":{"issn":["1864-5631"]},"publication_status":"published","issue":"22","year":"2015","intvolume":"         8","page":"3815-3822","citation":{"ieee":"W. Desens, C. Kohrt, M. Frank, and T. Werner, “Highly Efficient Polymer-Supported Catalytic System for the Valorization of Carbon Dioxide,” <i>ChemSusChem</i>, vol. 8, no. 22, pp. 3815–3822, 2015, doi: <a href=\"https://doi.org/10.1002/cssc.201501119\">10.1002/cssc.201501119</a>.","chicago":"Desens, Willi, Christina Kohrt, Marcus Frank, and Thomas Werner. “Highly Efficient Polymer-Supported Catalytic System for the Valorization of Carbon Dioxide.” <i>ChemSusChem</i> 8, no. 22 (2015): 3815–22. <a href=\"https://doi.org/10.1002/cssc.201501119\">https://doi.org/10.1002/cssc.201501119</a>.","ama":"Desens W, Kohrt C, Frank M, Werner T. Highly Efficient Polymer-Supported Catalytic System for the Valorization of Carbon Dioxide. <i>ChemSusChem</i>. 2015;8(22):3815-3822. doi:<a href=\"https://doi.org/10.1002/cssc.201501119\">10.1002/cssc.201501119</a>","bibtex":"@article{Desens_Kohrt_Frank_Werner_2015, title={Highly Efficient Polymer-Supported Catalytic System for the Valorization of Carbon Dioxide}, volume={8}, DOI={<a href=\"https://doi.org/10.1002/cssc.201501119\">10.1002/cssc.201501119</a>}, number={22}, journal={ChemSusChem}, publisher={Wiley}, author={Desens, Willi and Kohrt, Christina and Frank, Marcus and Werner, Thomas}, year={2015}, pages={3815–3822} }","short":"W. Desens, C. Kohrt, M. Frank, T. 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