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F., Andexer, J., Arenz, C., Beifuss, U., Beuerle, F., Brasholz, M., Breinbauer, R., Ditrich, K., Gulder, T. A. M., Hüttel, W., Kordes, M., Krueger, A., Lehmann, M., Lindel, T., Luy, B., Meier, M. A. R., Mück-Lichtenfeld, C., Muhle-Goll, C., Müller, T. J. J., … Worgull, D. (2017). Organische Chemie 2016. <i>Nachrichten Aus Der Chemie</i>, <i>65</i>(3), 266–304. <a href=\"https://doi.org/10.1002/nadc.20174059831\">https://doi.org/10.1002/nadc.20174059831</a>","short":"B.F. Straub, J. Andexer, C. Arenz, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, K. Ditrich, T.A.M. Gulder, W. Hüttel, M. Kordes, A. Krueger, M. Lehmann, T. Lindel, B. Luy, M.A.R. Meier, C. Mück-Lichtenfeld, C. Muhle-Goll, T.J.J. Müller, A. Narine, J. Paradies, R. Pfau, J. Pietruszka, N. Schaschke, M.O. Senge, T. Werner, D.B. Werz, C.A. Winter, D. 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Organische Chemie 2016. <i>Nachrichten aus der Chemie</i>. 2017;65(3):266-304. doi:<a href=\"https://doi.org/10.1002/nadc.20174059831\">10.1002/nadc.20174059831</a>","ieee":"B. F. 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Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides. <i>Green Chemistry</i>. 2017;19(18):4435-4445. doi:<a href=\"https://doi.org/10.1039/c7gc01782k\">10.1039/c7gc01782k</a>","bibtex":"@article{Steinbauer_Longwitz_Frank_Epping_Kragl_Werner_2017, title={Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides}, volume={19}, DOI={<a href=\"https://doi.org/10.1039/c7gc01782k\">10.1039/c7gc01782k</a>}, number={18}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Steinbauer, J. and Longwitz, L. and Frank, M. and Epping, J. and Kragl, U. and Werner, Thomas}, year={2017}, pages={4435–4445} }","mla":"Steinbauer, J., et al. “Immobilized Bifunctional Phosphonium Salts as Recyclable Organocatalysts in the Cycloaddition of CO<sub>2</sub> and Epoxides.” <i>Green Chemistry</i>, vol. 19, no. 18, Royal Society of Chemistry (RSC), 2017, pp. 4435–45, doi:<a href=\"https://doi.org/10.1039/c7gc01782k\">10.1039/c7gc01782k</a>.","short":"J. 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Werner, Green Chemistry 19 (2017) 3769–3779.","mla":"Steinbauer, J., et al. “An in Situ Formed Ca<sup>2+</sup>–Crown Ether Complex and Its Use in CO<sub>2</sub>-Fixation Reactions with Terminal and Internal Epoxides.” <i>Green Chemistry</i>, vol. 19, no. 16, Royal Society of Chemistry (RSC), 2017, pp. 3769–79, doi:<a href=\"https://doi.org/10.1039/c7gc01114h\">10.1039/c7gc01114h</a>.","apa":"Steinbauer, J., Spannenberg, A., &#38; Werner, T. (2017). An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides. <i>Green Chemistry</i>, <i>19</i>(16), 3769–3779. <a href=\"https://doi.org/10.1039/c7gc01114h\">https://doi.org/10.1039/c7gc01114h</a>"},"page":"3769-3779","intvolume":"        19","year":"2017","issue":"16","publication_status":"published","publication_identifier":{"issn":["1463-9262","1463-9270"]},"language":[{"iso":"eng"}],"extern":"1","keyword":["T1","T3","CSSD"],"user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37975","status":"public","abstract":[{"lang":"eng","text":"<p>Calcium punched beyond its weight: An <italic>in situ</italic> formed Ca<sup>2+</sup>–crown ether complex showed unprecedented efficiency in cyclic carbonate synthesis.</p>"}],"type":"journal_article","publication":"Green Chemistry"},{"date_created":"2023-01-22T20:59:56Z","author":[{"last_name":"Büttner","full_name":"Büttner, Hendrik","first_name":"Hendrik"},{"last_name":"Longwitz","full_name":"Longwitz, Lars","first_name":"Lars"},{"first_name":"Johannes","full_name":"Steinbauer, Johannes","last_name":"Steinbauer"},{"first_name":"Christoph","last_name":"Wulf","full_name":"Wulf, Christoph"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner"}],"volume":375,"date_updated":"2025-11-10T09:17:38Z","publisher":"Springer Science and Business Media LLC","doi":"10.1007/s41061-017-0136-5","title":"Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2","issue":"3","publication_status":"published","publication_identifier":{"issn":["2365-0869","2364-8961"]},"citation":{"apa":"Büttner, H., Longwitz, L., Steinbauer, J., Wulf, C., &#38; Werner, T. 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Werner, “Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2,” <i>Topics in Current Chemistry</i>, vol. 375, no. 3, Art. no. 50, 2017, doi: <a href=\"https://doi.org/10.1007/s41061-017-0136-5\">10.1007/s41061-017-0136-5</a>.","chicago":"Büttner, Hendrik, Lars Longwitz, Johannes Steinbauer, Christoph Wulf, and Thomas Werner. “Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2.” <i>Topics in Current Chemistry</i> 375, no. 3 (2017). <a href=\"https://doi.org/10.1007/s41061-017-0136-5\">https://doi.org/10.1007/s41061-017-0136-5</a>.","ama":"Büttner H, Longwitz L, Steinbauer J, Wulf C, Werner T. 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B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds. <i>Organic Letters</i>. 2017;19(21):5768-5771. doi:<a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">10.1021/acs.orglett.7b02701</a>","ieee":"W. Li, M.-M. Wang, Y. Hu, and T. Werner, “B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds,” <i>Organic Letters</i>, vol. 19, no. 21, pp. 5768–5771, 2017, doi: <a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">10.1021/acs.orglett.7b02701</a>.","chicago":"Li, Wu, Ming-Ming Wang, Yuya Hu, and Thomas Werner. “B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds.” <i>Organic Letters</i> 19, no. 21 (2017): 5768–71. <a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">https://doi.org/10.1021/acs.orglett.7b02701</a>.","apa":"Li, W., Wang, M.-M., Hu, Y., &#38; Werner, T. (2017). B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds. <i>Organic Letters</i>, <i>19</i>(21), 5768–5771. <a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">https://doi.org/10.1021/acs.orglett.7b02701</a>","bibtex":"@article{Li_Wang_Hu_Werner_2017, title={B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds}, volume={19}, DOI={<a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">10.1021/acs.orglett.7b02701</a>}, number={21}, journal={Organic Letters}, publisher={American Chemical Society (ACS)}, author={Li, Wu and Wang, Ming-Ming and Hu, Yuya and Werner, Thomas}, year={2017}, pages={5768–5771} }","short":"W. Li, M.-M. Wang, Y. Hu, T. Werner, Organic Letters 19 (2017) 5768–5771.","mla":"Li, Wu, et al. “B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds.” <i>Organic Letters</i>, vol. 19, no. 21, American Chemical Society (ACS), 2017, pp. 5768–71, doi:<a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">10.1021/acs.orglett.7b02701</a>."},"page":"5768-5771","intvolume":"        19","year":"2017","issue":"21","publication_status":"published","publication_identifier":{"issn":["1523-7060","1523-7052"]},"doi":"10.1021/acs.orglett.7b02701","title":"B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds","author":[{"last_name":"Li","full_name":"Li, Wu","first_name":"Wu"},{"last_name":"Wang","full_name":"Wang, Ming-Ming","first_name":"Ming-Ming"},{"full_name":"Hu, Yuya","last_name":"Hu","first_name":"Yuya"},{"full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"date_created":"2023-01-22T20:57:15Z","volume":19,"publisher":"American Chemical Society (ACS)","date_updated":"2025-11-10T09:18:33Z"},{"publication_status":"published","publication_identifier":{"issn":["1864-5631"]},"citation":{"ieee":"H. Büttner, J. Steinbauer, C. Wulf, M. Dindaroglu, H.-G. Schmalz, and T. Werner, “Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables,” <i>ChemSusChem</i>, vol. 10, no. 6, pp. 1076–1079, 2017, doi: <a href=\"https://doi.org/10.1002/cssc.201601163\">10.1002/cssc.201601163</a>.","chicago":"Büttner, Hendrik, Johannes Steinbauer, Christoph Wulf, Mehmet Dindaroglu, Hans-Günther Schmalz, and Thomas Werner. “Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables.” <i>ChemSusChem</i> 10, no. 6 (2017): 1076–79. <a href=\"https://doi.org/10.1002/cssc.201601163\">https://doi.org/10.1002/cssc.201601163</a>.","ama":"Büttner H, Steinbauer J, Wulf C, Dindaroglu M, Schmalz H-G, Werner T. Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables. <i>ChemSusChem</i>. 2017;10(6):1076-1079. doi:<a href=\"https://doi.org/10.1002/cssc.201601163\">10.1002/cssc.201601163</a>","mla":"Büttner, Hendrik, et al. “Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables.” <i>ChemSusChem</i>, vol. 10, no. 6, Wiley, 2017, pp. 1076–79, doi:<a href=\"https://doi.org/10.1002/cssc.201601163\">10.1002/cssc.201601163</a>.","short":"H. Büttner, J. Steinbauer, C. Wulf, M. Dindaroglu, H.-G. Schmalz, T. Werner, ChemSusChem 10 (2017) 1076–1079.","bibtex":"@article{Büttner_Steinbauer_Wulf_Dindaroglu_Schmalz_Werner_2017, title={Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables}, volume={10}, DOI={<a href=\"https://doi.org/10.1002/cssc.201601163\">10.1002/cssc.201601163</a>}, number={6}, journal={ChemSusChem}, publisher={Wiley}, author={Büttner, Hendrik and Steinbauer, Johannes and Wulf, Christoph and Dindaroglu, Mehmet and Schmalz, Hans-Günther and Werner, Thomas}, year={2017}, pages={1076–1079} }","apa":"Büttner, H., Steinbauer, J., Wulf, C., Dindaroglu, M., Schmalz, H.-G., &#38; Werner, T. (2017). Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables. <i>ChemSusChem</i>, <i>10</i>(6), 1076–1079. <a href=\"https://doi.org/10.1002/cssc.201601163\">https://doi.org/10.1002/cssc.201601163</a>"},"page":"1076-1079","intvolume":"        10","author":[{"full_name":"Büttner, Hendrik","last_name":"Büttner","first_name":"Hendrik"},{"last_name":"Steinbauer","full_name":"Steinbauer, Johannes","first_name":"Johannes"},{"first_name":"Christoph","last_name":"Wulf","full_name":"Wulf, Christoph"},{"full_name":"Dindaroglu, Mehmet","last_name":"Dindaroglu","first_name":"Mehmet"},{"first_name":"Hans-Günther","last_name":"Schmalz","full_name":"Schmalz, Hans-Günther"},{"full_name":"Werner, Thomas","id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"volume":10,"date_updated":"2025-11-10T09:17:59Z","doi":"10.1002/cssc.201601163","type":"journal_article","status":"public","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37978","extern":"1","issue":"6","year":"2017","date_created":"2023-01-22T21:00:17Z","publisher":"Wiley","title":"Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables","publication":"ChemSusChem","language":[{"iso":"eng"}],"keyword":["T1","T2","CSSD"]},{"type":"journal_article","status":"public","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37974","extern":"1","publication_identifier":{"issn":["1864-5631"]},"publication_status":"published","page":"3025-3029","intvolume":"        10","citation":{"ama":"Steinbauer J, Werner T. Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis. <i>ChemSusChem</i>. 2017;10(15):3025-3029. doi:<a href=\"https://doi.org/10.1002/cssc.201700788\">10.1002/cssc.201700788</a>","ieee":"J. Steinbauer and T. Werner, “Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis,” <i>ChemSusChem</i>, vol. 10, no. 15, pp. 3025–3029, 2017, doi: <a href=\"https://doi.org/10.1002/cssc.201700788\">10.1002/cssc.201700788</a>.","chicago":"Steinbauer, Johannes, and Thomas Werner. “Poly(Ethylene Glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis.” <i>ChemSusChem</i> 10, no. 15 (2017): 3025–29. <a href=\"https://doi.org/10.1002/cssc.201700788\">https://doi.org/10.1002/cssc.201700788</a>.","mla":"Steinbauer, Johannes, and Thomas Werner. “Poly(Ethylene Glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis.” <i>ChemSusChem</i>, vol. 10, no. 15, Wiley, 2017, pp. 3025–29, doi:<a href=\"https://doi.org/10.1002/cssc.201700788\">10.1002/cssc.201700788</a>.","bibtex":"@article{Steinbauer_Werner_2017, title={Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis}, volume={10}, DOI={<a href=\"https://doi.org/10.1002/cssc.201700788\">10.1002/cssc.201700788</a>}, number={15}, journal={ChemSusChem}, publisher={Wiley}, author={Steinbauer, Johannes and Werner, Thomas}, year={2017}, pages={3025–3029} }","short":"J. Steinbauer, T. Werner, ChemSusChem 10 (2017) 3025–3029.","apa":"Steinbauer, J., &#38; Werner, T. (2017). Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis. <i>ChemSusChem</i>, <i>10</i>(15), 3025–3029. <a href=\"https://doi.org/10.1002/cssc.201700788\">https://doi.org/10.1002/cssc.201700788</a>"},"volume":10,"author":[{"first_name":"Johannes","full_name":"Steinbauer, Johannes","last_name":"Steinbauer"},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"date_updated":"2025-11-10T09:17:48Z","doi":"10.1002/cssc.201700788","publication":"ChemSusChem","language":[{"iso":"eng"}],"keyword":["T1","T3","CSSD"],"issue":"15","year":"2017","date_created":"2023-01-22T20:58:02Z","publisher":"Wiley","title":"Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis"}]