[{"date_created":"2023-01-22T20:38:11Z","publisher":"Wiley","title":"Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>","issue":"7","year":"2020","language":[{"iso":"eng"}],"keyword":["T2","T1","CSSD"],"publication":"ChemSusChem","author":[{"full_name":"Hu, Yuya","last_name":"Hu","first_name":"Yuya"},{"first_name":"Sandra","last_name":"Peglow","full_name":"Peglow, Sandra"},{"full_name":"Longwitz, Lars","last_name":"Longwitz","first_name":"Lars"},{"full_name":"Frank, Marcus","last_name":"Frank","first_name":"Marcus"},{"last_name":"Epping","full_name":"Epping, Jan Dirk","first_name":"Jan Dirk"},{"full_name":"Brüser, Volker","last_name":"Brüser","first_name":"Volker"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"volume":13,"date_updated":"2025-11-10T08:50:25Z","doi":"10.1002/cssc.201903384","publication_status":"published","publication_identifier":{"issn":["1864-5631","1864-564X"]},"citation":{"apa":"Hu, Y., Peglow, S., Longwitz, L., Frank, M., Epping, J. D., Brüser, V., &#38; Werner, T. (2020). Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>. <i>ChemSusChem</i>, <i>13</i>(7), 1825–1833. <a href=\"https://doi.org/10.1002/cssc.201903384\">https://doi.org/10.1002/cssc.201903384</a>","bibtex":"@article{Hu_Peglow_Longwitz_Frank_Epping_Brüser_Werner_2020, title={Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>}, volume={13}, DOI={<a href=\"https://doi.org/10.1002/cssc.201903384\">10.1002/cssc.201903384</a>}, number={7}, journal={ChemSusChem}, publisher={Wiley}, author={Hu, Yuya and Peglow, Sandra and Longwitz, Lars and Frank, Marcus and Epping, Jan Dirk and Brüser, Volker and Werner, Thomas}, year={2020}, pages={1825–1833} }","short":"Y. Hu, S. Peglow, L. Longwitz, M. Frank, J.D. Epping, V. Brüser, T. Werner, ChemSusChem 13 (2020) 1825–1833.","mla":"Hu, Yuya, et al. “Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>.” <i>ChemSusChem</i>, vol. 13, no. 7, Wiley, 2020, pp. 1825–33, doi:<a href=\"https://doi.org/10.1002/cssc.201903384\">10.1002/cssc.201903384</a>.","chicago":"Hu, Yuya, Sandra Peglow, Lars Longwitz, Marcus Frank, Jan Dirk Epping, Volker Brüser, and Thomas Werner. “Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>.” <i>ChemSusChem</i> 13, no. 7 (2020): 1825–33. <a href=\"https://doi.org/10.1002/cssc.201903384\">https://doi.org/10.1002/cssc.201903384</a>.","ieee":"Y. Hu <i>et al.</i>, “Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>,” <i>ChemSusChem</i>, vol. 13, no. 7, pp. 1825–1833, 2020, doi: <a href=\"https://doi.org/10.1002/cssc.201903384\">10.1002/cssc.201903384</a>.","ama":"Hu Y, Peglow S, Longwitz L, et al. Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>. <i>ChemSusChem</i>. 2020;13(7):1825-1833. doi:<a href=\"https://doi.org/10.1002/cssc.201903384\">10.1002/cssc.201903384</a>"},"intvolume":"        13","page":"1825-1833","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37953","extern":"1","type":"journal_article","status":"public"},{"publication_identifier":{"issn":["0968-0896"]},"publication_status":"published","issue":"11","year":"2020","intvolume":"        28","citation":{"ama":"Grandane A, Nocentini A, Werner T, Zalubovskis R, Supuran CT. Benzoxepinones: A new isoform-selective class of tumor associated carbonic anhydrase inhibitors. <i>Bioorganic and Medicinal Chemistry</i>. 2020;28(11). doi:<a href=\"https://doi.org/10.1016/j.bmc.2020.115496\">10.1016/j.bmc.2020.115496</a>","ieee":"A. Grandane, A. Nocentini, T. Werner, R. Zalubovskis, and C. T. Supuran, “Benzoxepinones: A new isoform-selective class of tumor associated carbonic anhydrase inhibitors,” <i>Bioorganic and Medicinal Chemistry</i>, vol. 28, no. 11, Art. no. 115496, 2020, doi: <a href=\"https://doi.org/10.1016/j.bmc.2020.115496\">10.1016/j.bmc.2020.115496</a>.","chicago":"Grandane, Aiga, Alessio Nocentini, Thomas Werner, Raivis Zalubovskis, and Claudiu T. Supuran. “Benzoxepinones: A New Isoform-Selective Class of Tumor Associated Carbonic Anhydrase Inhibitors.” <i>Bioorganic and Medicinal Chemistry</i> 28, no. 11 (2020). <a href=\"https://doi.org/10.1016/j.bmc.2020.115496\">https://doi.org/10.1016/j.bmc.2020.115496</a>.","apa":"Grandane, A., Nocentini, A., Werner, T., Zalubovskis, R., &#38; Supuran, C. T. (2020). Benzoxepinones: A new isoform-selective class of tumor associated carbonic anhydrase inhibitors. <i>Bioorganic and Medicinal Chemistry</i>, <i>28</i>(11), Article 115496. <a href=\"https://doi.org/10.1016/j.bmc.2020.115496\">https://doi.org/10.1016/j.bmc.2020.115496</a>","mla":"Grandane, Aiga, et al. “Benzoxepinones: A New Isoform-Selective Class of Tumor Associated Carbonic Anhydrase Inhibitors.” <i>Bioorganic and Medicinal Chemistry</i>, vol. 28, no. 11, 115496, Elsevier BV, 2020, doi:<a href=\"https://doi.org/10.1016/j.bmc.2020.115496\">10.1016/j.bmc.2020.115496</a>.","short":"A. Grandane, A. Nocentini, T. Werner, R. Zalubovskis, C.T. Supuran, Bioorganic and Medicinal Chemistry 28 (2020).","bibtex":"@article{Grandane_Nocentini_Werner_Zalubovskis_Supuran_2020, title={Benzoxepinones: A new isoform-selective class of tumor associated carbonic anhydrase inhibitors}, volume={28}, DOI={<a href=\"https://doi.org/10.1016/j.bmc.2020.115496\">10.1016/j.bmc.2020.115496</a>}, number={11115496}, journal={Bioorganic and Medicinal Chemistry}, publisher={Elsevier BV}, author={Grandane, Aiga and Nocentini, Alessio and Werner, Thomas and Zalubovskis, Raivis and Supuran, Claudiu T.}, year={2020} }"},"publisher":"Elsevier BV","date_updated":"2025-11-10T08:51:24Z","volume":28,"author":[{"last_name":"Grandane","full_name":"Grandane, Aiga","first_name":"Aiga"},{"last_name":"Nocentini","full_name":"Nocentini, Alessio","first_name":"Alessio"},{"orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"},{"first_name":"Raivis","full_name":"Zalubovskis, Raivis","last_name":"Zalubovskis"},{"full_name":"Supuran, Claudiu T.","last_name":"Supuran","first_name":"Claudiu T."}],"date_created":"2023-01-22T20:36:02Z","title":"Benzoxepinones: A new isoform-selective class of tumor associated carbonic anhydrase inhibitors","doi":"10.1016/j.bmc.2020.115496","publication":"Bioorganic and Medicinal Chemistry","type":"journal_article","status":"public","_id":"37952","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","keyword":["T4","T2","CSSD"],"article_number":"115496","language":[{"iso":"eng"}],"extern":"1"},{"publisher":"American Chemical Society (ACS)","date_created":"2023-01-22T20:41:56Z","title":"Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature","issue":"10","year":"2019","keyword":["T2","CSSD"],"language":[{"iso":"eng"}],"publication":"ACS Catalysis","date_updated":"2025-11-10T08:54:03Z","author":[{"first_name":"Lars","full_name":"Longwitz, Lars","last_name":"Longwitz"},{"full_name":"Spannenberg, Anke","last_name":"Spannenberg","first_name":"Anke"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"volume":9,"doi":"10.1021/acscatal.9b02456","publication_status":"published","publication_identifier":{"issn":["2155-5435","2155-5435"]},"citation":{"ama":"Longwitz L, Spannenberg A, Werner T. Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature. <i>ACS Catalysis</i>. 2019;9(10):9237-9244. doi:<a href=\"https://doi.org/10.1021/acscatal.9b02456\">10.1021/acscatal.9b02456</a>","ieee":"L. Longwitz, A. Spannenberg, and T. Werner, “Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature,” <i>ACS Catalysis</i>, vol. 9, no. 10, pp. 9237–9244, 2019, doi: <a href=\"https://doi.org/10.1021/acscatal.9b02456\">10.1021/acscatal.9b02456</a>.","chicago":"Longwitz, Lars, Anke Spannenberg, and Thomas Werner. “Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature.” <i>ACS Catalysis</i> 9, no. 10 (2019): 9237–44. <a href=\"https://doi.org/10.1021/acscatal.9b02456\">https://doi.org/10.1021/acscatal.9b02456</a>.","apa":"Longwitz, L., Spannenberg, A., &#38; Werner, T. (2019). Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature. <i>ACS Catalysis</i>, <i>9</i>(10), 9237–9244. <a href=\"https://doi.org/10.1021/acscatal.9b02456\">https://doi.org/10.1021/acscatal.9b02456</a>","bibtex":"@article{Longwitz_Spannenberg_Werner_2019, title={Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature}, volume={9}, DOI={<a href=\"https://doi.org/10.1021/acscatal.9b02456\">10.1021/acscatal.9b02456</a>}, number={10}, journal={ACS Catalysis}, publisher={American Chemical Society (ACS)}, author={Longwitz, Lars and Spannenberg, Anke and Werner, Thomas}, year={2019}, pages={9237–9244} }","short":"L. Longwitz, A. Spannenberg, T. Werner, ACS Catalysis 9 (2019) 9237–9244.","mla":"Longwitz, Lars, et al. “Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature.” <i>ACS Catalysis</i>, vol. 9, no. 10, American Chemical Society (ACS), 2019, pp. 9237–44, doi:<a href=\"https://doi.org/10.1021/acscatal.9b02456\">10.1021/acscatal.9b02456</a>."},"page":"9237-9244","intvolume":"         9","_id":"37958","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"extern":"1","type":"journal_article","status":"public"},{"title":"Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts","publisher":"Royal Society of Chemistry (RSC)","date_created":"2023-01-22T20:43:38Z","year":"2019","issue":"19","keyword":["T3","CSSD"],"language":[{"iso":"eng"}],"abstract":[{"text":"<p>The reduction of poly and cyclic carbonates in the presence of an earth abundant metal catalyst using isopropanol as the hydrogen donor is reported.</p>","lang":"eng"}],"publication":"Green Chemistry","doi":"10.1039/c9gc02052g","date_updated":"2025-11-10T08:55:06Z","author":[{"last_name":"Liu","full_name":"Liu, Xin","first_name":"Xin"},{"full_name":"de Vries, Johannes G.","last_name":"de Vries","first_name":"Johannes G."},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"volume":21,"citation":{"apa":"Liu, X., de Vries, J. G., &#38; Werner, T. (2019). Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts. <i>Green Chemistry</i>, <i>21</i>(19), 5248–5255. <a href=\"https://doi.org/10.1039/c9gc02052g\">https://doi.org/10.1039/c9gc02052g</a>","mla":"Liu, Xin, et al. “Transfer Hydrogenation of Cyclic Carbonates and Polycarbonate to Methanol and Diols by Iron Pincer Catalysts.” <i>Green Chemistry</i>, vol. 21, no. 19, Royal Society of Chemistry (RSC), 2019, pp. 5248–55, doi:<a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>.","bibtex":"@article{Liu_de Vries_Werner_2019, title={Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts}, volume={21}, DOI={<a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>}, number={19}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Liu, Xin and de Vries, Johannes G. and Werner, Thomas}, year={2019}, pages={5248–5255} }","short":"X. Liu, J.G. de Vries, T. Werner, Green Chemistry 21 (2019) 5248–5255.","chicago":"Liu, Xin, Johannes G. de Vries, and Thomas Werner. “Transfer Hydrogenation of Cyclic Carbonates and Polycarbonate to Methanol and Diols by Iron Pincer Catalysts.” <i>Green Chemistry</i> 21, no. 19 (2019): 5248–55. <a href=\"https://doi.org/10.1039/c9gc02052g\">https://doi.org/10.1039/c9gc02052g</a>.","ieee":"X. Liu, J. G. de Vries, and T. Werner, “Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts,” <i>Green Chemistry</i>, vol. 21, no. 19, pp. 5248–5255, 2019, doi: <a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>.","ama":"Liu X, de Vries JG, Werner T. Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts. <i>Green Chemistry</i>. 2019;21(19):5248-5255. doi:<a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>"},"page":"5248-5255","intvolume":"        21","publication_status":"published","publication_identifier":{"issn":["1463-9262","1463-9270"]},"extern":"1","_id":"37961","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"status":"public","type":"journal_article"},{"type":"journal_article","publication":"ChemSusChem","status":"public","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37963","language":[{"iso":"eng"}],"extern":"1","keyword":["T1","T4","CSSD"],"issue":"12","publication_status":"published","publication_identifier":{"issn":["1864-5631","1864-564X"]},"citation":{"chicago":"Büttner, Hendrik, Christina Kohrt, Christoph Wulf, Benjamin Schäffner, Karsten Groenke, Yuya Hu, Daniela Kruse, and Thomas Werner. “Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate.” <i>ChemSusChem</i> 12, no. 12 (2019): 2701–7. <a href=\"https://doi.org/10.1002/cssc.201900678\">https://doi.org/10.1002/cssc.201900678</a>.","ieee":"H. Büttner <i>et al.</i>, “Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate,” <i>ChemSusChem</i>, vol. 12, no. 12, pp. 2701–2707, 2019, doi: <a href=\"https://doi.org/10.1002/cssc.201900678\">10.1002/cssc.201900678</a>.","ama":"Büttner H, Kohrt C, Wulf C, et al. Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate. <i>ChemSusChem</i>. 2019;12(12):2701-2707. doi:<a href=\"https://doi.org/10.1002/cssc.201900678\">10.1002/cssc.201900678</a>","apa":"Büttner, H., Kohrt, C., Wulf, C., Schäffner, B., Groenke, K., Hu, Y., Kruse, D., &#38; Werner, T. (2019). Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate. <i>ChemSusChem</i>, <i>12</i>(12), 2701–2707. <a href=\"https://doi.org/10.1002/cssc.201900678\">https://doi.org/10.1002/cssc.201900678</a>","bibtex":"@article{Büttner_Kohrt_Wulf_Schäffner_Groenke_Hu_Kruse_Werner_2019, title={Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate}, volume={12}, DOI={<a href=\"https://doi.org/10.1002/cssc.201900678\">10.1002/cssc.201900678</a>}, number={12}, journal={ChemSusChem}, publisher={Wiley}, author={Büttner, Hendrik and Kohrt, Christina and Wulf, Christoph and Schäffner, Benjamin and Groenke, Karsten and Hu, Yuya and Kruse, Daniela and Werner, Thomas}, year={2019}, pages={2701–2707} }","short":"H. Büttner, C. Kohrt, C. Wulf, B. Schäffner, K. Groenke, Y. Hu, D. Kruse, T. Werner, ChemSusChem 12 (2019) 2701–2707.","mla":"Büttner, Hendrik, et al. “Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate.” <i>ChemSusChem</i>, vol. 12, no. 12, Wiley, 2019, pp. 2701–07, doi:<a href=\"https://doi.org/10.1002/cssc.201900678\">10.1002/cssc.201900678</a>."},"intvolume":"        12","page":"2701-2707","year":"2019","date_created":"2023-01-22T20:44:24Z","author":[{"first_name":"Hendrik","full_name":"Büttner, Hendrik","last_name":"Büttner"},{"first_name":"Christina","last_name":"Kohrt","full_name":"Kohrt, Christina"},{"full_name":"Wulf, Christoph","last_name":"Wulf","first_name":"Christoph"},{"full_name":"Schäffner, Benjamin","last_name":"Schäffner","first_name":"Benjamin"},{"full_name":"Groenke, Karsten","last_name":"Groenke","first_name":"Karsten"},{"first_name":"Yuya","full_name":"Hu, Yuya","last_name":"Hu"},{"last_name":"Kruse","full_name":"Kruse, Daniela","first_name":"Daniela"},{"orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"volume":12,"publisher":"Wiley","date_updated":"2025-11-10T08:56:56Z","doi":"10.1002/cssc.201900678","title":"Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate"},{"title":"Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis","publisher":"American Chemical Society (ACS)","date_created":"2023-01-22T20:41:19Z","year":"2019","issue":"15","keyword":["T1","T3","CSSD"],"language":[{"iso":"eng"}],"publication":"ACS Sustainable Chemistry and Engineering","doi":"10.1021/acssuschemeng.9b02502","date_updated":"2025-11-10T08:55:33Z","volume":7,"author":[{"first_name":"Yuya","full_name":"Hu, Yuya","last_name":"Hu"},{"first_name":"Johannes","last_name":"Steinbauer","full_name":"Steinbauer, Johannes"},{"last_name":"Stefanow","full_name":"Stefanow, Vivian","first_name":"Vivian"},{"first_name":"Anke","full_name":"Spannenberg, Anke","last_name":"Spannenberg"},{"last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271","first_name":"Thomas"}],"page":"13257-13269","intvolume":"         7","citation":{"ama":"Hu Y, Steinbauer J, Stefanow V, Spannenberg A, Werner T. Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis. <i>ACS Sustainable Chemistry and Engineering</i>. 2019;7(15):13257-13269. doi:<a href=\"https://doi.org/10.1021/acssuschemeng.9b02502\">10.1021/acssuschemeng.9b02502</a>","ieee":"Y. Hu, J. Steinbauer, V. Stefanow, A. Spannenberg, and T. Werner, “Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis,” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 7, no. 15, pp. 13257–13269, 2019, doi: <a href=\"https://doi.org/10.1021/acssuschemeng.9b02502\">10.1021/acssuschemeng.9b02502</a>.","chicago":"Hu, Yuya, Johannes Steinbauer, Vivian Stefanow, Anke Spannenberg, and Thomas Werner. “Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis.” <i>ACS Sustainable Chemistry and Engineering</i> 7, no. 15 (2019): 13257–69. <a href=\"https://doi.org/10.1021/acssuschemeng.9b02502\">https://doi.org/10.1021/acssuschemeng.9b02502</a>.","apa":"Hu, Y., Steinbauer, J., Stefanow, V., Spannenberg, A., &#38; Werner, T. (2019). Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis. <i>ACS Sustainable Chemistry and Engineering</i>, <i>7</i>(15), 13257–13269. <a href=\"https://doi.org/10.1021/acssuschemeng.9b02502\">https://doi.org/10.1021/acssuschemeng.9b02502</a>","bibtex":"@article{Hu_Steinbauer_Stefanow_Spannenberg_Werner_2019, title={Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis}, volume={7}, DOI={<a href=\"https://doi.org/10.1021/acssuschemeng.9b02502\">10.1021/acssuschemeng.9b02502</a>}, number={15}, journal={ACS Sustainable Chemistry and Engineering}, publisher={American Chemical Society (ACS)}, author={Hu, Yuya and Steinbauer, Johannes and Stefanow, Vivian and Spannenberg, Anke and Werner, Thomas}, year={2019}, pages={13257–13269} }","short":"Y. Hu, J. Steinbauer, V. Stefanow, A. Spannenberg, T. Werner, ACS Sustainable Chemistry and Engineering 7 (2019) 13257–13269.","mla":"Hu, Yuya, et al. “Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis.” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 7, no. 15, American Chemical Society (ACS), 2019, pp. 13257–69, doi:<a href=\"https://doi.org/10.1021/acssuschemeng.9b02502\">10.1021/acssuschemeng.9b02502</a>."},"publication_identifier":{"issn":["2168-0485","2168-0485"]},"publication_status":"published","extern":"1","_id":"37957","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","status":"public","type":"journal_article"},{"status":"public","type":"journal_article","publication":"The Journal of Organic Chemistry","keyword":["T2","CSSD"],"language":[{"iso":"eng"}],"extern":"1","_id":"37962","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"year":"2019","citation":{"apa":"Longwitz, L., Jopp, S., &#38; Werner, T. (2019). Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling. <i>The Journal of Organic Chemistry</i>, <i>84</i>(12), 7863–7870. <a href=\"https://doi.org/10.1021/acs.joc.9b00741\">https://doi.org/10.1021/acs.joc.9b00741</a>","short":"L. Longwitz, S. Jopp, T. Werner, The Journal of Organic Chemistry 84 (2019) 7863–7870.","mla":"Longwitz, Lars, et al. “Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling.” <i>The Journal of Organic Chemistry</i>, vol. 84, no. 12, American Chemical Society (ACS), 2019, pp. 7863–70, doi:<a href=\"https://doi.org/10.1021/acs.joc.9b00741\">10.1021/acs.joc.9b00741</a>.","bibtex":"@article{Longwitz_Jopp_Werner_2019, title={Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling}, volume={84}, DOI={<a href=\"https://doi.org/10.1021/acs.joc.9b00741\">10.1021/acs.joc.9b00741</a>}, number={12}, journal={The Journal of Organic Chemistry}, publisher={American Chemical Society (ACS)}, author={Longwitz, Lars and Jopp, Stefan and Werner, Thomas}, year={2019}, pages={7863–7870} }","ama":"Longwitz L, Jopp S, Werner T. Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling. <i>The Journal of Organic Chemistry</i>. 2019;84(12):7863-7870. doi:<a href=\"https://doi.org/10.1021/acs.joc.9b00741\">10.1021/acs.joc.9b00741</a>","ieee":"L. Longwitz, S. Jopp, and T. Werner, “Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling,” <i>The Journal of Organic Chemistry</i>, vol. 84, no. 12, pp. 7863–7870, 2019, doi: <a href=\"https://doi.org/10.1021/acs.joc.9b00741\">10.1021/acs.joc.9b00741</a>.","chicago":"Longwitz, Lars, Stefan Jopp, and Thomas Werner. “Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling.” <i>The Journal of Organic Chemistry</i> 84, no. 12 (2019): 7863–70. <a href=\"https://doi.org/10.1021/acs.joc.9b00741\">https://doi.org/10.1021/acs.joc.9b00741</a>."},"intvolume":"        84","page":"7863-7870","publication_status":"published","publication_identifier":{"issn":["0022-3263","1520-6904"]},"issue":"12","title":"Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling","doi":"10.1021/acs.joc.9b00741","publisher":"American Chemical Society (ACS)","date_updated":"2025-11-10T08:54:28Z","date_created":"2023-01-22T20:44:02Z","author":[{"last_name":"Longwitz","full_name":"Longwitz, Lars","first_name":"Lars"},{"first_name":"Stefan","last_name":"Jopp","full_name":"Jopp, Stefan"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"volume":84},{"publication":"Science","abstract":[{"lang":"eng","text":"<jats:p>Catalytic nucleophilic substitution of alcohols makes organic synthesis greener</jats:p>"}],"keyword":["T2","CSSD"],"language":[{"iso":"eng"}],"issue":"6456","year":"2019","publisher":"American Association for the Advancement of Science (AAAS)","date_created":"2023-01-22T20:42:20Z","title":"The Mitsunobu reaction, reimagined","type":"journal_article","status":"public","_id":"37959","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","publication_identifier":{"issn":["0036-8075","1095-9203"]},"publication_status":"published","intvolume":"       365","page":"866-867","citation":{"apa":"Longwitz, L., &#38; Werner, T. (2019). The Mitsunobu reaction, reimagined. <i>Science</i>, <i>365</i>(6456), 866–867. <a href=\"https://doi.org/10.1126/science.aay6635\">https://doi.org/10.1126/science.aay6635</a>","short":"L. Longwitz, T. Werner, Science 365 (2019) 866–867.","bibtex":"@article{Longwitz_Werner_2019, title={The Mitsunobu reaction, reimagined}, volume={365}, DOI={<a href=\"https://doi.org/10.1126/science.aay6635\">10.1126/science.aay6635</a>}, number={6456}, journal={Science}, publisher={American Association for the Advancement of Science (AAAS)}, author={Longwitz, Lars and Werner, Thomas}, year={2019}, pages={866–867} }","mla":"Longwitz, Lars, and Thomas Werner. “The Mitsunobu Reaction, Reimagined.” <i>Science</i>, vol. 365, no. 6456, American Association for the Advancement of Science (AAAS), 2019, pp. 866–67, doi:<a href=\"https://doi.org/10.1126/science.aay6635\">10.1126/science.aay6635</a>.","chicago":"Longwitz, Lars, and Thomas Werner. “The Mitsunobu Reaction, Reimagined.” <i>Science</i> 365, no. 6456 (2019): 866–67. <a href=\"https://doi.org/10.1126/science.aay6635\">https://doi.org/10.1126/science.aay6635</a>.","ieee":"L. Longwitz and T. Werner, “The Mitsunobu reaction, reimagined,” <i>Science</i>, vol. 365, no. 6456, pp. 866–867, 2019, doi: <a href=\"https://doi.org/10.1126/science.aay6635\">10.1126/science.aay6635</a>.","ama":"Longwitz L, Werner T. The Mitsunobu reaction, reimagined. <i>Science</i>. 2019;365(6456):866-867. doi:<a href=\"https://doi.org/10.1126/science.aay6635\">10.1126/science.aay6635</a>"},"date_updated":"2025-11-10T09:01:38Z","volume":365,"author":[{"first_name":"Lars","full_name":"Longwitz, Lars","last_name":"Longwitz"},{"full_name":"Werner, Thomas","id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"doi":"10.1126/science.aay6635"},{"publication":"ACS Catalysis","language":[{"iso":"eng"}],"keyword":["T4","CSSD"],"year":"2019","issue":"9","title":"Catalytic Approaches to Monomers for Polymers Based on Renewables","date_created":"2023-01-22T20:42:48Z","publisher":"American Chemical Society (ACS)","status":"public","type":"journal_article","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37960","citation":{"short":"B.M. Stadler, C. Wulf, T. Werner, S. Tin, J.G. de Vries, ACS Catalysis 9 (2019) 8012–8067.","bibtex":"@article{Stadler_Wulf_Werner_Tin_de Vries_2019, title={Catalytic Approaches to Monomers for Polymers Based on Renewables}, volume={9}, DOI={<a href=\"https://doi.org/10.1021/acscatal.9b01665\">10.1021/acscatal.9b01665</a>}, number={9}, journal={ACS Catalysis}, publisher={American Chemical Society (ACS)}, author={Stadler, Bernhard M. and Wulf, Christoph and Werner, Thomas and Tin, Sergey and de Vries, Johannes G.}, year={2019}, pages={8012–8067} }","mla":"Stadler, Bernhard M., et al. “Catalytic Approaches to Monomers for Polymers Based on Renewables.” <i>ACS Catalysis</i>, vol. 9, no. 9, American Chemical Society (ACS), 2019, pp. 8012–67, doi:<a href=\"https://doi.org/10.1021/acscatal.9b01665\">10.1021/acscatal.9b01665</a>.","apa":"Stadler, B. M., Wulf, C., Werner, T., Tin, S., &#38; de Vries, J. G. (2019). Catalytic Approaches to Monomers for Polymers Based on Renewables. <i>ACS Catalysis</i>, <i>9</i>(9), 8012–8067. <a href=\"https://doi.org/10.1021/acscatal.9b01665\">https://doi.org/10.1021/acscatal.9b01665</a>","ama":"Stadler BM, Wulf C, Werner T, Tin S, de Vries JG. Catalytic Approaches to Monomers for Polymers Based on Renewables. <i>ACS Catalysis</i>. 2019;9(9):8012-8067. doi:<a href=\"https://doi.org/10.1021/acscatal.9b01665\">10.1021/acscatal.9b01665</a>","chicago":"Stadler, Bernhard M., Christoph Wulf, Thomas Werner, Sergey Tin, and Johannes G. de Vries. “Catalytic Approaches to Monomers for Polymers Based on Renewables.” <i>ACS Catalysis</i> 9, no. 9 (2019): 8012–67. <a href=\"https://doi.org/10.1021/acscatal.9b01665\">https://doi.org/10.1021/acscatal.9b01665</a>.","ieee":"B. M. Stadler, C. Wulf, T. Werner, S. Tin, and J. G. de Vries, “Catalytic Approaches to Monomers for Polymers Based on Renewables,” <i>ACS Catalysis</i>, vol. 9, no. 9, pp. 8012–8067, 2019, doi: <a href=\"https://doi.org/10.1021/acscatal.9b01665\">10.1021/acscatal.9b01665</a>."},"page":"8012-8067","intvolume":"         9","publication_status":"published","publication_identifier":{"issn":["2155-5435","2155-5435"]},"doi":"10.1021/acscatal.9b01665","author":[{"last_name":"Stadler","full_name":"Stadler, Bernhard M.","first_name":"Bernhard M."},{"last_name":"Wulf","full_name":"Wulf, Christoph","first_name":"Christoph"},{"orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"},{"full_name":"Tin, Sergey","last_name":"Tin","first_name":"Sergey"},{"first_name":"Johannes G.","full_name":"de Vries, Johannes G.","last_name":"de Vries"}],"volume":9,"date_updated":"2025-11-10T09:01:51Z"},{"status":"public","abstract":[{"text":"<jats:title>Abstract</jats:title>\r\n               <jats:p>Numerous organic transformations are based on the use of stoichiometric amounts of phosphorus reagents. The formation of phosphane oxides from phosphanes is usually the thermodynamic driving force for these reactions. The stoichiometric amounts of phosphane oxide which are formed as by-products often significantly hamper the product purification. Organophosphorus catalysis based on P(III)/P(V) redox cycling aims to address these problems. Herein we present our recent advances in developing catalytic Wittig-type reactions. More specifically, we reported our results on catalytic Wittig reactions based on readily available Bu<jats:sub>3</jats:sub>P=O as pre-catalyst as well as the first microwave-assisted version of this reaction and the first enantioselective catalytic Wittig reaction utilizing chiral phosphane catalysts. Further developments led to the implementation of catalytic base-free Wittig reactions yielding highly functionalized alkylidene and arylidene succinates.</jats:p>","lang":"eng"}],"publication":"Pure and Applied Chemistry","type":"journal_article","extern":"1","language":[{"iso":"eng"}],"keyword":["T2","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37966","page":"95-102","intvolume":"        91","citation":{"ieee":"L. Longwitz and T. Werner, “Recent advances in catalytic Wittig-type reactions based on P(III)/P(V) redox cycling,” <i>Pure and Applied Chemistry</i>, vol. 91, no. 1, pp. 95–102, 2019, doi: <a href=\"https://doi.org/10.1515/pac-2018-0920\">10.1515/pac-2018-0920</a>.","chicago":"Longwitz, Lars, and Thomas Werner. “Recent Advances in Catalytic Wittig-Type Reactions Based on P(III)/P(V) Redox Cycling.” <i>Pure and Applied Chemistry</i> 91, no. 1 (2019): 95–102. <a href=\"https://doi.org/10.1515/pac-2018-0920\">https://doi.org/10.1515/pac-2018-0920</a>.","ama":"Longwitz L, Werner T. Recent advances in catalytic Wittig-type reactions based on P(III)/P(V) redox cycling. <i>Pure and Applied Chemistry</i>. 2019;91(1):95-102. doi:<a href=\"https://doi.org/10.1515/pac-2018-0920\">10.1515/pac-2018-0920</a>","apa":"Longwitz, L., &#38; Werner, T. (2019). Recent advances in catalytic Wittig-type reactions based on P(III)/P(V) redox cycling. <i>Pure and Applied Chemistry</i>, <i>91</i>(1), 95–102. <a href=\"https://doi.org/10.1515/pac-2018-0920\">https://doi.org/10.1515/pac-2018-0920</a>","mla":"Longwitz, Lars, and Thomas Werner. “Recent Advances in Catalytic Wittig-Type Reactions Based on P(III)/P(V) Redox Cycling.” <i>Pure and Applied Chemistry</i>, vol. 91, no. 1, Walter de Gruyter GmbH, 2019, pp. 95–102, doi:<a href=\"https://doi.org/10.1515/pac-2018-0920\">10.1515/pac-2018-0920</a>.","bibtex":"@article{Longwitz_Werner_2019, title={Recent advances in catalytic Wittig-type reactions based on P(III)/P(V) redox cycling}, volume={91}, DOI={<a href=\"https://doi.org/10.1515/pac-2018-0920\">10.1515/pac-2018-0920</a>}, number={1}, journal={Pure and Applied Chemistry}, publisher={Walter de Gruyter GmbH}, author={Longwitz, Lars and Werner, Thomas}, year={2019}, pages={95–102} }","short":"L. Longwitz, T. Werner, Pure and Applied Chemistry 91 (2019) 95–102."},"year":"2019","issue":"1","publication_identifier":{"issn":["1365-3075","0033-4545"]},"publication_status":"published","doi":"10.1515/pac-2018-0920","title":"Recent advances in catalytic Wittig-type reactions based on P(III)/P(V) redox cycling","volume":91,"date_created":"2023-01-22T20:45:38Z","author":[{"last_name":"Longwitz","full_name":"Longwitz, Lars","first_name":"Lars"},{"id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"date_updated":"2025-11-10T09:06:58Z","publisher":"Walter de Gruyter GmbH"},{"publication":"The Journal of Organic Chemistry","language":[{"iso":"eng"}],"keyword":["T2","T4","CSSD"],"issue":"3","year":"2019","date_created":"2023-01-22T20:45:12Z","publisher":"American Chemical Society (ACS)","title":"Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones","type":"journal_article","status":"public","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37965","extern":"1","publication_identifier":{"issn":["0022-3263","1520-6904"]},"publication_status":"published","intvolume":"        84","page":"1320-1329","citation":{"ieee":"A. Grandane <i>et al.</i>, “Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones,” <i>The Journal of Organic Chemistry</i>, vol. 84, no. 3, pp. 1320–1329, 2019, doi: <a href=\"https://doi.org/10.1021/acs.joc.8b02789\">10.1021/acs.joc.8b02789</a>.","chicago":"Grandane, Aiga, Lars Longwitz, Catrin Roolf, Anke Spannenberg, Hugo Murua Escobar, Christian Junghanss, Edgars Suna, and Thomas Werner. “Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones.” <i>The Journal of Organic Chemistry</i> 84, no. 3 (2019): 1320–29. <a href=\"https://doi.org/10.1021/acs.joc.8b02789\">https://doi.org/10.1021/acs.joc.8b02789</a>.","ama":"Grandane A, Longwitz L, Roolf C, et al. Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones. <i>The Journal of Organic Chemistry</i>. 2019;84(3):1320-1329. doi:<a href=\"https://doi.org/10.1021/acs.joc.8b02789\">10.1021/acs.joc.8b02789</a>","short":"A. Grandane, L. Longwitz, C. Roolf, A. Spannenberg, H. Murua Escobar, C. Junghanss, E. Suna, T. Werner, The Journal of Organic Chemistry 84 (2019) 1320–1329.","bibtex":"@article{Grandane_Longwitz_Roolf_Spannenberg_Murua Escobar_Junghanss_Suna_Werner_2019, title={Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones}, volume={84}, DOI={<a href=\"https://doi.org/10.1021/acs.joc.8b02789\">10.1021/acs.joc.8b02789</a>}, number={3}, journal={The Journal of Organic Chemistry}, publisher={American Chemical Society (ACS)}, author={Grandane, Aiga and Longwitz, Lars and Roolf, Catrin and Spannenberg, Anke and Murua Escobar, Hugo and Junghanss, Christian and Suna, Edgars and Werner, Thomas}, year={2019}, pages={1320–1329} }","mla":"Grandane, Aiga, et al. “Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones.” <i>The Journal of Organic Chemistry</i>, vol. 84, no. 3, American Chemical Society (ACS), 2019, pp. 1320–29, doi:<a href=\"https://doi.org/10.1021/acs.joc.8b02789\">10.1021/acs.joc.8b02789</a>.","apa":"Grandane, A., Longwitz, L., Roolf, C., Spannenberg, A., Murua Escobar, H., Junghanss, C., Suna, E., &#38; Werner, T. (2019). Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones. <i>The Journal of Organic Chemistry</i>, <i>84</i>(3), 1320–1329. <a href=\"https://doi.org/10.1021/acs.joc.8b02789\">https://doi.org/10.1021/acs.joc.8b02789</a>"},"volume":84,"author":[{"first_name":"Aiga","full_name":"Grandane, Aiga","last_name":"Grandane"},{"first_name":"Lars","last_name":"Longwitz","full_name":"Longwitz, Lars"},{"full_name":"Roolf, Catrin","last_name":"Roolf","first_name":"Catrin"},{"full_name":"Spannenberg, Anke","last_name":"Spannenberg","first_name":"Anke"},{"first_name":"Hugo","full_name":"Murua Escobar, Hugo","last_name":"Murua Escobar"},{"full_name":"Junghanss, Christian","last_name":"Junghanss","first_name":"Christian"},{"last_name":"Suna","full_name":"Suna, Edgars","first_name":"Edgars"},{"orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"date_updated":"2025-11-10T09:10:18Z","doi":"10.1021/acs.joc.8b02789"},{"year":"2018","issue":"8","title":"Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach","date_created":"2023-01-22T20:46:04Z","publisher":"American Chemical Society (ACS)","publication":"ACS Sustainable Chemistry and Engineering","language":[{"iso":"eng"}],"keyword":["T1","T2","CSSD"],"citation":{"short":"J. Steinbauer, C. Kubis, R. Ludwig, T. Werner, ACS Sustainable Chemistry and Engineering 6 (2018) 10778–10788.","bibtex":"@article{Steinbauer_Kubis_Ludwig_Werner_2018, title={Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach}, volume={6}, DOI={<a href=\"https://doi.org/10.1021/acssuschemeng.8b02093\">10.1021/acssuschemeng.8b02093</a>}, number={8}, journal={ACS Sustainable Chemistry and Engineering}, publisher={American Chemical Society (ACS)}, author={Steinbauer, Johannes and Kubis, Christoph and Ludwig, Ralf and Werner, Thomas}, year={2018}, pages={10778–10788} }","mla":"Steinbauer, Johannes, et al. “Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach.” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 6, no. 8, American Chemical Society (ACS), 2018, pp. 10778–88, doi:<a href=\"https://doi.org/10.1021/acssuschemeng.8b02093\">10.1021/acssuschemeng.8b02093</a>.","apa":"Steinbauer, J., Kubis, C., Ludwig, R., &#38; Werner, T. (2018). Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach. <i>ACS Sustainable Chemistry and Engineering</i>, <i>6</i>(8), 10778–10788. <a href=\"https://doi.org/10.1021/acssuschemeng.8b02093\">https://doi.org/10.1021/acssuschemeng.8b02093</a>","ama":"Steinbauer J, Kubis C, Ludwig R, Werner T. Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach. <i>ACS Sustainable Chemistry and Engineering</i>. 2018;6(8):10778-10788. doi:<a href=\"https://doi.org/10.1021/acssuschemeng.8b02093\">10.1021/acssuschemeng.8b02093</a>","chicago":"Steinbauer, Johannes, Christoph Kubis, Ralf Ludwig, and Thomas Werner. “Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach.” <i>ACS Sustainable Chemistry and Engineering</i> 6, no. 8 (2018): 10778–88. <a href=\"https://doi.org/10.1021/acssuschemeng.8b02093\">https://doi.org/10.1021/acssuschemeng.8b02093</a>.","ieee":"J. Steinbauer, C. Kubis, R. Ludwig, and T. Werner, “Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach,” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 6, no. 8, pp. 10778–10788, 2018, doi: <a href=\"https://doi.org/10.1021/acssuschemeng.8b02093\">10.1021/acssuschemeng.8b02093</a>."},"page":"10778-10788","intvolume":"         6","publication_status":"published","publication_identifier":{"issn":["2168-0485","2168-0485"]},"doi":"10.1021/acssuschemeng.8b02093","author":[{"first_name":"Johannes","last_name":"Steinbauer","full_name":"Steinbauer, Johannes"},{"first_name":"Christoph","full_name":"Kubis, Christoph","last_name":"Kubis"},{"first_name":"Ralf","full_name":"Ludwig, Ralf","last_name":"Ludwig"},{"id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"volume":6,"date_updated":"2025-11-10T09:04:50Z","status":"public","type":"journal_article","extern":"1","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37967"},{"intvolume":"         8","page":"3673-3679","citation":{"chicago":"Wulf, Christoph, Ulrike Doering, and Thomas Werner. “Copolymerization of CO<sub>2</sub> and Epoxides Mediated by Zinc Organyls.” <i>RSC Advances</i> 8, no. 7 (2018): 3673–79. <a href=\"https://doi.org/10.1039/c7ra12535f\">https://doi.org/10.1039/c7ra12535f</a>.","ieee":"C. Wulf, U. Doering, and T. Werner, “Copolymerization of CO<sub>2</sub> and epoxides mediated by zinc organyls,” <i>RSC Advances</i>, vol. 8, no. 7, pp. 3673–3679, 2018, doi: <a href=\"https://doi.org/10.1039/c7ra12535f\">10.1039/c7ra12535f</a>.","ama":"Wulf C, Doering U, Werner T. Copolymerization of CO<sub>2</sub> and epoxides mediated by zinc organyls. <i>RSC Advances</i>. 2018;8(7):3673-3679. doi:<a href=\"https://doi.org/10.1039/c7ra12535f\">10.1039/c7ra12535f</a>","short":"C. Wulf, U. Doering, T. Werner, RSC Advances 8 (2018) 3673–3679.","mla":"Wulf, Christoph, et al. “Copolymerization of CO<sub>2</sub> and Epoxides Mediated by Zinc Organyls.” <i>RSC Advances</i>, vol. 8, no. 7, Royal Society of Chemistry (RSC), 2018, pp. 3673–79, doi:<a href=\"https://doi.org/10.1039/c7ra12535f\">10.1039/c7ra12535f</a>.","bibtex":"@article{Wulf_Doering_Werner_2018, title={Copolymerization of CO<sub>2</sub> and epoxides mediated by zinc organyls}, volume={8}, DOI={<a href=\"https://doi.org/10.1039/c7ra12535f\">10.1039/c7ra12535f</a>}, number={7}, journal={RSC Advances}, publisher={Royal Society of Chemistry (RSC)}, author={Wulf, Christoph and Doering, Ulrike and Werner, Thomas}, year={2018}, pages={3673–3679} }","apa":"Wulf, C., Doering, U., &#38; Werner, T. (2018). Copolymerization of CO<sub>2</sub> and epoxides mediated by zinc organyls. <i>RSC Advances</i>, <i>8</i>(7), 3673–3679. <a href=\"https://doi.org/10.1039/c7ra12535f\">https://doi.org/10.1039/c7ra12535f</a>"},"year":"2018","issue":"7","publication_identifier":{"issn":["2046-2069"]},"publication_status":"published","doi":"10.1039/c7ra12535f","title":"Copolymerization of CO<sub>2</sub> and epoxides mediated by zinc organyls","volume":8,"date_created":"2023-01-22T20:46:56Z","author":[{"full_name":"Wulf, Christoph","last_name":"Wulf","first_name":"Christoph"},{"full_name":"Doering, Ulrike","last_name":"Doering","first_name":"Ulrike"},{"last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271","first_name":"Thomas"}],"publisher":"Royal Society of Chemistry (RSC)","date_updated":"2025-11-10T09:03:07Z","status":"public","abstract":[{"lang":"eng","text":"<p>Simple zinc organyls (R<sub>2</sub>Zn) efficiently catalyze the copolymerization of CO<sub>2</sub> and cyclohexene oxide. The effect of various reaction parameters has been studied. The reaction proceeds under halogen-free conditions and no co-catalyst is required.</p>"}],"publication":"RSC Advances","type":"journal_article","extern":"1","language":[{"iso":"eng"}],"keyword":["T1","T3","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37969"},{"doi":"10.1021/acscatal.7b03367","date_updated":"2025-11-10T09:05:26Z","volume":8,"author":[{"full_name":"Longwitz, Lars","last_name":"Longwitz","first_name":"Lars"},{"first_name":"Johannes","last_name":"Steinbauer","full_name":"Steinbauer, Johannes"},{"full_name":"Spannenberg, Anke","last_name":"Spannenberg","first_name":"Anke"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"intvolume":"         8","page":"665-672","citation":{"mla":"Longwitz, Lars, et al. “Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions.” <i>ACS Catalysis</i>, vol. 8, no. 1, American Chemical Society (ACS), 2018, pp. 665–72, doi:<a href=\"https://doi.org/10.1021/acscatal.7b03367\">10.1021/acscatal.7b03367</a>.","bibtex":"@article{Longwitz_Steinbauer_Spannenberg_Werner_2018, title={Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions}, volume={8}, DOI={<a href=\"https://doi.org/10.1021/acscatal.7b03367\">10.1021/acscatal.7b03367</a>}, number={1}, journal={ACS Catalysis}, publisher={American Chemical Society (ACS)}, author={Longwitz, Lars and Steinbauer, Johannes and Spannenberg, Anke and Werner, Thomas}, year={2018}, pages={665–672} }","short":"L. Longwitz, J. Steinbauer, A. Spannenberg, T. Werner, ACS Catalysis 8 (2018) 665–672.","apa":"Longwitz, L., Steinbauer, J., Spannenberg, A., &#38; Werner, T. (2018). Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions. <i>ACS Catalysis</i>, <i>8</i>(1), 665–672. <a href=\"https://doi.org/10.1021/acscatal.7b03367\">https://doi.org/10.1021/acscatal.7b03367</a>","ama":"Longwitz L, Steinbauer J, Spannenberg A, Werner T. Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions. <i>ACS Catalysis</i>. 2018;8(1):665-672. doi:<a href=\"https://doi.org/10.1021/acscatal.7b03367\">10.1021/acscatal.7b03367</a>","chicago":"Longwitz, Lars, Johannes Steinbauer, Anke Spannenberg, and Thomas Werner. “Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions.” <i>ACS Catalysis</i> 8, no. 1 (2018): 665–72. <a href=\"https://doi.org/10.1021/acscatal.7b03367\">https://doi.org/10.1021/acscatal.7b03367</a>.","ieee":"L. Longwitz, J. Steinbauer, A. Spannenberg, and T. Werner, “Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions,” <i>ACS Catalysis</i>, vol. 8, no. 1, pp. 665–672, 2018, doi: <a href=\"https://doi.org/10.1021/acscatal.7b03367\">10.1021/acscatal.7b03367</a>."},"publication_identifier":{"issn":["2155-5435","2155-5435"]},"publication_status":"published","_id":"62105","department":[{"_id":"35"},{"_id":"2"}],"user_id":"89271","status":"public","type":"journal_article","title":"Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions","publisher":"American Chemical Society (ACS)","date_created":"2025-11-05T15:47:56Z","year":"2018","issue":"1","keyword":["T1","T3","T4","CSSD"],"language":[{"iso":"eng"}],"publication":"ACS Catalysis"},{"date_updated":"2025-11-10T09:14:45Z","author":[{"full_name":"Li, Wu","last_name":"Li","first_name":"Wu"},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"volume":19,"doi":"10.1021/acs.orglett.7b00720","publication_status":"published","publication_identifier":{"issn":["1523-7060","1523-7052"]},"citation":{"chicago":"Li, Wu, and Thomas Werner. “B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles.” <i>Organic Letters</i> 19, no. 10 (2017): 2568–71. <a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">https://doi.org/10.1021/acs.orglett.7b00720</a>.","ieee":"W. Li and T. Werner, “B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles,” <i>Organic Letters</i>, vol. 19, no. 10, pp. 2568–2571, 2017, doi: <a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">10.1021/acs.orglett.7b00720</a>.","ama":"Li W, Werner T. B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles. <i>Organic Letters</i>. 2017;19(10):2568-2571. doi:<a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">10.1021/acs.orglett.7b00720</a>","apa":"Li, W., &#38; Werner, T. (2017). B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles. <i>Organic Letters</i>, <i>19</i>(10), 2568–2571. <a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">https://doi.org/10.1021/acs.orglett.7b00720</a>","short":"W. Li, T. Werner, Organic Letters 19 (2017) 2568–2571.","mla":"Li, Wu, and Thomas Werner. “B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles.” <i>Organic Letters</i>, vol. 19, no. 10, American Chemical Society (ACS), 2017, pp. 2568–71, doi:<a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">10.1021/acs.orglett.7b00720</a>.","bibtex":"@article{Li_Werner_2017, title={B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles}, volume={19}, DOI={<a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">10.1021/acs.orglett.7b00720</a>}, number={10}, journal={Organic Letters}, publisher={American Chemical Society (ACS)}, author={Li, Wu and Werner, Thomas}, year={2017}, pages={2568–2571} }"},"intvolume":"        19","page":"2568-2571","_id":"37976","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"extern":"1","type":"journal_article","status":"public","publisher":"American Chemical Society (ACS)","date_created":"2023-01-22T20:59:34Z","title":"B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles","issue":"10","year":"2017","keyword":["CSSD"],"language":[{"iso":"eng"}],"publication":"Organic Letters"},{"title":"Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides","doi":"10.1039/c7gc01782k","date_updated":"2025-11-10T09:18:10Z","publisher":"Royal Society of Chemistry (RSC)","volume":19,"date_created":"2023-01-22T20:57:38Z","author":[{"full_name":"Steinbauer, J.","last_name":"Steinbauer","first_name":"J."},{"first_name":"L.","full_name":"Longwitz, L.","last_name":"Longwitz"},{"last_name":"Frank","full_name":"Frank, M.","first_name":"M."},{"first_name":"J.","full_name":"Epping, J.","last_name":"Epping"},{"full_name":"Kragl, U.","last_name":"Kragl","first_name":"U."},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas"}],"year":"2017","intvolume":"        19","page":"4435-4445","citation":{"ama":"Steinbauer J, Longwitz L, Frank M, Epping J, Kragl U, Werner T. 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>","chicago":"Steinbauer, J., L. Longwitz, M. Frank, J. Epping, U. Kragl, and Thomas Werner. “Immobilized Bifunctional Phosphonium Salts as Recyclable Organocatalysts in the Cycloaddition of CO<sub>2</sub> and Epoxides.” <i>Green Chemistry</i> 19, no. 18 (2017): 4435–45. <a href=\"https://doi.org/10.1039/c7gc01782k\">https://doi.org/10.1039/c7gc01782k</a>.","ieee":"J. Steinbauer, L. Longwitz, M. Frank, J. Epping, U. Kragl, and T. Werner, “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, pp. 4435–4445, 2017, doi: <a href=\"https://doi.org/10.1039/c7gc01782k\">10.1039/c7gc01782k</a>.","short":"J. Steinbauer, L. Longwitz, M. Frank, J. Epping, U. Kragl, T. Werner, Green Chemistry 19 (2017) 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>.","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} }","apa":"Steinbauer, J., Longwitz, L., Frank, M., Epping, J., Kragl, U., &#38; Werner, T. (2017). Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides. <i>Green Chemistry</i>, <i>19</i>(18), 4435–4445. <a href=\"https://doi.org/10.1039/c7gc01782k\">https://doi.org/10.1039/c7gc01782k</a>"},"publication_identifier":{"issn":["1463-9262","1463-9270"]},"publication_status":"published","issue":"18","keyword":["T1","T2","CSSD"],"extern":"1","language":[{"iso":"eng"}],"_id":"37973","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","abstract":[{"lang":"eng","text":"<p>An immobilized bifunctional phosphonium salt catalyst efficiently catalyzed the synthesis of cyclic carbonates under mild conditions, and was reused up to 15 times.</p>"}],"status":"public","publication":"Green Chemistry","type":"journal_article"},{"page":"3769-3779","intvolume":"        19","citation":{"ieee":"J. Steinbauer, A. Spannenberg, and T. Werner, “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, pp. 3769–3779, 2017, doi: <a href=\"https://doi.org/10.1039/c7gc01114h\">10.1039/c7gc01114h</a>.","chicago":"Steinbauer, J., A. Spannenberg, and Thomas Werner. “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> 19, no. 16 (2017): 3769–79. <a href=\"https://doi.org/10.1039/c7gc01114h\">https://doi.org/10.1039/c7gc01114h</a>.","ama":"Steinbauer J, Spannenberg A, Werner T. 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>. 2017;19(16):3769-3779. 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>","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>.","bibtex":"@article{Steinbauer_Spannenberg_Werner_2017, title={An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides}, volume={19}, DOI={<a href=\"https://doi.org/10.1039/c7gc01114h\">10.1039/c7gc01114h</a>}, number={16}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Steinbauer, J. and Spannenberg, A. and Werner, Thomas}, year={2017}, pages={3769–3779} }","short":"J. Steinbauer, A. Spannenberg, T. Werner, Green Chemistry 19 (2017) 3769–3779."},"year":"2017","issue":"16","publication_identifier":{"issn":["1463-9262","1463-9270"]},"publication_status":"published","doi":"10.1039/c7gc01114h","title":"An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides","volume":19,"author":[{"first_name":"J.","full_name":"Steinbauer, J.","last_name":"Steinbauer"},{"first_name":"A.","full_name":"Spannenberg, A.","last_name":"Spannenberg"},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner"}],"date_created":"2023-01-22T20:59:12Z","publisher":"Royal Society of Chemistry (RSC)","date_updated":"2025-11-10T09:18:18Z","status":"public","abstract":[{"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>","lang":"eng"}],"publication":"Green Chemistry","type":"journal_article","extern":"1","language":[{"iso":"eng"}],"keyword":["T1","T3","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37975"},{"title":"Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2","doi":"10.1007/s41061-017-0136-5","date_updated":"2025-11-10T09:17:38Z","publisher":"Springer Science and Business Media LLC","author":[{"full_name":"Büttner, Hendrik","last_name":"Büttner","first_name":"Hendrik"},{"first_name":"Lars","full_name":"Longwitz, Lars","last_name":"Longwitz"},{"last_name":"Steinbauer","full_name":"Steinbauer, Johannes","first_name":"Johannes"},{"first_name":"Christoph","full_name":"Wulf, Christoph","last_name":"Wulf"},{"full_name":"Werner, Thomas","id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"date_created":"2023-01-22T20:59:56Z","volume":375,"year":"2017","citation":{"apa":"Büttner, H., Longwitz, L., Steinbauer, J., Wulf, C., &#38; Werner, T. (2017). Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2. <i>Topics in Current Chemistry</i>, <i>375</i>(3), Article 50. <a href=\"https://doi.org/10.1007/s41061-017-0136-5\">https://doi.org/10.1007/s41061-017-0136-5</a>","short":"H. Büttner, L. Longwitz, J. Steinbauer, C. Wulf, T. Werner, Topics in Current Chemistry 375 (2017).","mla":"Büttner, Hendrik, et al. “Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2.” <i>Topics in Current Chemistry</i>, vol. 375, no. 3, 50, Springer Science and Business Media LLC, 2017, doi:<a href=\"https://doi.org/10.1007/s41061-017-0136-5\">10.1007/s41061-017-0136-5</a>.","bibtex":"@article{Büttner_Longwitz_Steinbauer_Wulf_Werner_2017, title={Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2}, volume={375}, DOI={<a href=\"https://doi.org/10.1007/s41061-017-0136-5\">10.1007/s41061-017-0136-5</a>}, number={350}, journal={Topics in Current Chemistry}, publisher={Springer Science and Business Media LLC}, author={Büttner, Hendrik and Longwitz, Lars and Steinbauer, Johannes and Wulf, Christoph and Werner, Thomas}, year={2017} }","ama":"Büttner H, Longwitz L, Steinbauer J, Wulf C, Werner T. Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2. <i>Topics in Current Chemistry</i>. 2017;375(3). 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>.","ieee":"H. Büttner, L. Longwitz, J. Steinbauer, C. Wulf, and T. 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>."},"intvolume":"       375","publication_status":"published","publication_identifier":{"issn":["2365-0869","2364-8961"]},"issue":"3","article_number":"50","keyword":["T1","CSSD"],"extern":"1","language":[{"iso":"eng"}],"_id":"37977","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"status":"public","type":"journal_article","publication":"Topics in Current Chemistry"},{"year":"2017","citation":{"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>.","ama":"Li W, Wang M-M, Hu Y, Werner T. 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>","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>","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>.","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} }"},"intvolume":"        19","page":"5768-5771","publication_status":"published","publication_identifier":{"issn":["1523-7060","1523-7052"]},"issue":"21","title":"B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds","doi":"10.1021/acs.orglett.7b02701","date_updated":"2025-11-10T09:18:33Z","publisher":"American Chemical Society (ACS)","author":[{"first_name":"Wu","full_name":"Li, Wu","last_name":"Li"},{"first_name":"Ming-Ming","full_name":"Wang, Ming-Ming","last_name":"Wang"},{"full_name":"Hu, Yuya","last_name":"Hu","first_name":"Yuya"},{"orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"date_created":"2023-01-22T20:57:15Z","volume":19,"status":"public","type":"journal_article","publication":"Organic Letters","keyword":["CSSD"],"language":[{"iso":"eng"}],"extern":"1","_id":"37972","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}]},{"keyword":["T1","T2","CSSD"],"language":[{"iso":"eng"}],"publication":"ChemSusChem","publisher":"Wiley","date_created":"2023-01-22T21:00:17Z","title":"Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables","issue":"6","year":"2017","_id":"37978","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","extern":"1","type":"journal_article","status":"public","date_updated":"2025-11-10T09:17:59Z","volume":10,"author":[{"first_name":"Hendrik","last_name":"Büttner","full_name":"Büttner, Hendrik"},{"first_name":"Johannes","last_name":"Steinbauer","full_name":"Steinbauer, Johannes"},{"last_name":"Wulf","full_name":"Wulf, Christoph","first_name":"Christoph"},{"first_name":"Mehmet","full_name":"Dindaroglu, Mehmet","last_name":"Dindaroglu"},{"last_name":"Schmalz","full_name":"Schmalz, Hans-Günther","first_name":"Hans-Günther"},{"id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"doi":"10.1002/cssc.201601163","publication_identifier":{"issn":["1864-5631"]},"publication_status":"published","intvolume":"        10","page":"1076-1079","citation":{"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>","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>.","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>","short":"H. Büttner, J. Steinbauer, C. Wulf, M. Dindaroglu, H.-G. Schmalz, T. Werner, ChemSusChem 10 (2017) 1076–1079.","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>.","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} }"}}]