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