[{"doi":"10.1021/acscatal.9b01665","volume":9,"author":[{"last_name":"Stadler","full_name":"Stadler, Bernhard M.","first_name":"Bernhard M."},{"last_name":"Wulf","full_name":"Wulf, Christoph","first_name":"Christoph"},{"id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"},{"first_name":"Sergey","full_name":"Tin, Sergey","last_name":"Tin"},{"full_name":"de Vries, Johannes G.","last_name":"de Vries","first_name":"Johannes G."}],"date_updated":"2025-11-10T09:01:51Z","intvolume":"         9","page":"8012-8067","citation":{"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>.","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>","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} }","short":"B.M. Stadler, C. Wulf, T. Werner, S. Tin, J.G. de Vries, ACS Catalysis 9 (2019) 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>."},"publication_identifier":{"issn":["2155-5435","2155-5435"]},"publication_status":"published","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37960","status":"public","type":"journal_article","title":"Catalytic Approaches to Monomers for Polymers Based on Renewables","date_created":"2023-01-22T20:42:48Z","publisher":"American Chemical Society (ACS)","year":"2019","issue":"9","language":[{"iso":"eng"}],"keyword":["T4","CSSD"],"publication":"ACS Catalysis"},{"title":"Recent advances in catalytic Wittig-type reactions based on P(III)/P(V) redox cycling","doi":"10.1515/pac-2018-0920","date_updated":"2025-11-10T09:06:58Z","publisher":"Walter de Gruyter GmbH","volume":91,"author":[{"full_name":"Longwitz, Lars","last_name":"Longwitz","first_name":"Lars"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"date_created":"2023-01-22T20:45:38Z","year":"2019","intvolume":"        91","page":"95-102","citation":{"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} }","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>.","short":"L. Longwitz, T. Werner, Pure and Applied Chemistry 91 (2019) 95–102.","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>","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>","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>.","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>."},"publication_identifier":{"issn":["1365-3075","0033-4545"]},"publication_status":"published","issue":"1","keyword":["T2","CSSD"],"language":[{"iso":"eng"}],"extern":"1","_id":"37966","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","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"}],"status":"public","publication":"Pure and Applied Chemistry","type":"journal_article"},{"page":"1320-1329","intvolume":"        84","citation":{"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>","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>.","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} }","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.","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>"},"publication_identifier":{"issn":["0022-3263","1520-6904"]},"publication_status":"published","doi":"10.1021/acs.joc.8b02789","volume":84,"author":[{"last_name":"Grandane","full_name":"Grandane, Aiga","first_name":"Aiga"},{"last_name":"Longwitz","full_name":"Longwitz, Lars","first_name":"Lars"},{"last_name":"Roolf","full_name":"Roolf, Catrin","first_name":"Catrin"},{"first_name":"Anke","last_name":"Spannenberg","full_name":"Spannenberg, Anke"},{"last_name":"Murua Escobar","full_name":"Murua Escobar, Hugo","first_name":"Hugo"},{"full_name":"Junghanss, Christian","last_name":"Junghanss","first_name":"Christian"},{"last_name":"Suna","full_name":"Suna, Edgars","first_name":"Edgars"},{"full_name":"Werner, Thomas","id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"date_updated":"2025-11-10T09:10:18Z","status":"public","type":"journal_article","extern":"1","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37965","year":"2019","issue":"3","title":"Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones","date_created":"2023-01-22T20:45:12Z","publisher":"American Chemical Society (ACS)","publication":"The Journal of Organic Chemistry","language":[{"iso":"eng"}],"keyword":["T2","T4","CSSD"]},{"date_created":"2023-01-22T20:48:24Z","publisher":"Wiley","title":"Trendbericht Organische Chemie 2017","issue":"3","year":"2018","language":[{"iso":"eng"}],"keyword":["General Chemical Engineering","General Chemistry"],"publication":"Nachrichten aus der Chemie","volume":66,"author":[{"first_name":"Bernd","last_name":"Straub","full_name":"Straub, Bernd"},{"first_name":"Jennifer N.","last_name":"Andexer","full_name":"Andexer, Jennifer N."},{"last_name":"Arenz","full_name":"Arenz, Christoph","first_name":"Christoph"},{"full_name":"Beifuss, Uwe","last_name":"Beifuss","first_name":"Uwe"},{"full_name":"Beuerle, Florian","last_name":"Beuerle","first_name":"Florian"},{"full_name":"Brasholz, Malte","last_name":"Brasholz","first_name":"Malte"},{"first_name":"Rolf","full_name":"Breinbauer, Rolf","last_name":"Breinbauer"},{"first_name":"Klaus","last_name":"Ditrich","full_name":"Ditrich, Klaus"},{"first_name":"Martin","full_name":"Ernst, Martin","last_name":"Ernst"},{"last_name":"Gulder","full_name":"Gulder, Tobias A. M.","first_name":"Tobias A. M."},{"first_name":"Markus","last_name":"Kordes","full_name":"Kordes, Markus"},{"first_name":"Anke","last_name":"Krueger","full_name":"Krueger, Anke"},{"last_name":"Lehmann","full_name":"Lehmann, Matthias","first_name":"Matthias"},{"last_name":"Lindel","full_name":"Lindel, Thomas","first_name":"Thomas"},{"full_name":"Lüdeke, Steffen","last_name":"Lüdeke","first_name":"Steffen"},{"first_name":"Burkhard","full_name":"Luy, Burkhard","last_name":"Luy"},{"full_name":"Meier, Michael A. R.","last_name":"Meier","first_name":"Michael A. R."},{"full_name":"Mück-Lichtenfeld, Christian","last_name":"Mück-Lichtenfeld","first_name":"Christian"},{"full_name":"Muhle-Goll, Claudia","last_name":"Muhle-Goll","first_name":"Claudia"},{"full_name":"Narine, Arun","last_name":"Narine","first_name":"Arun"},{"full_name":"Paradies, Jan","id":"53339","orcid":"0000-0002-3698-668X","last_name":"Paradies","first_name":"Jan"},{"full_name":"Pfau, Roland","last_name":"Pfau","first_name":"Roland"},{"full_name":"Pietruszka, Jörg","last_name":"Pietruszka","first_name":"Jörg"},{"first_name":"Norbert","full_name":"Schaschke, Norbert","last_name":"Schaschke"},{"first_name":"Mathias O.","full_name":"Senge, Mathias O.","last_name":"Senge"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271","full_name":"Werner, Thomas"},{"full_name":"Werz, Daniel B.","last_name":"Werz","first_name":"Daniel B."},{"first_name":"Christian","full_name":"Winter, Christian","last_name":"Winter"},{"first_name":"Dennis","last_name":"Worgull","full_name":"Worgull, Dennis"}],"date_updated":"2025-11-10T09:03:49Z","doi":"10.1002/nadc.20184072148","publication_identifier":{"issn":["1439-9598"]},"publication_status":"published","page":"249-280","intvolume":"        66","citation":{"ieee":"B. Straub <i>et al.</i>, “Trendbericht Organische Chemie 2017,” <i>Nachrichten aus der Chemie</i>, vol. 66, no. 3, pp. 249–280, 2018, doi: <a href=\"https://doi.org/10.1002/nadc.20184072148\">10.1002/nadc.20184072148</a>.","chicago":"Straub, Bernd, Jennifer N. Andexer, Christoph Arenz, Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, et al. “Trendbericht Organische Chemie 2017.” <i>Nachrichten Aus Der Chemie</i> 66, no. 3 (2018): 249–80. <a href=\"https://doi.org/10.1002/nadc.20184072148\">https://doi.org/10.1002/nadc.20184072148</a>.","ama":"Straub B, Andexer JN, Arenz C, et al. Trendbericht Organische Chemie 2017. <i>Nachrichten aus der Chemie</i>. 2018;66(3):249-280. doi:<a href=\"https://doi.org/10.1002/nadc.20184072148\">10.1002/nadc.20184072148</a>","apa":"Straub, B., Andexer, J. N., Arenz, C., Beifuss, U., Beuerle, F., Brasholz, M., Breinbauer, R., Ditrich, K., Ernst, M., Gulder, T. A. M., Kordes, M., Krueger, A., Lehmann, M., Lindel, T., Lüdeke, S., Luy, B., Meier, M. A. R., Mück-Lichtenfeld, C., Muhle-Goll, C., … Worgull, D. (2018). Trendbericht Organische Chemie 2017. <i>Nachrichten Aus Der Chemie</i>, <i>66</i>(3), 249–280. <a href=\"https://doi.org/10.1002/nadc.20184072148\">https://doi.org/10.1002/nadc.20184072148</a>","bibtex":"@article{Straub_Andexer_Arenz_Beifuss_Beuerle_Brasholz_Breinbauer_Ditrich_Ernst_Gulder_et al._2018, title={Trendbericht Organische Chemie 2017}, volume={66}, DOI={<a href=\"https://doi.org/10.1002/nadc.20184072148\">10.1002/nadc.20184072148</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Straub, Bernd and Andexer, Jennifer N. and Arenz, Christoph and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ditrich, Klaus and Ernst, Martin and Gulder, Tobias A. M. and et al.}, year={2018}, pages={249–280} }","mla":"Straub, Bernd, et al. “Trendbericht Organische Chemie 2017.” <i>Nachrichten Aus Der Chemie</i>, vol. 66, no. 3, Wiley, 2018, pp. 249–80, doi:<a href=\"https://doi.org/10.1002/nadc.20184072148\">10.1002/nadc.20184072148</a>.","short":"B. Straub, J.N. Andexer, C. Arenz, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, K. Ditrich, M. Ernst, T.A.M. Gulder, M. Kordes, A. Krueger, M. Lehmann, T. Lindel, S. Lüdeke, B. Luy, M.A.R. Meier, C. Mück-Lichtenfeld, C. Muhle-Goll, A. Narine, J. Paradies, R. Pfau, J. Pietruszka, N. Schaschke, M.O. Senge, T. Werner, D.B. Werz, C. Winter, D. Worgull, Nachrichten Aus Der Chemie 66 (2018) 249–280."},"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"},{"_id":"389"}],"user_id":"89271","_id":"37971","extern":"1","type":"journal_article","status":"public"},{"citation":{"ama":"Hu Y, Yin Z, Werner T, Spannenberg A, Wu X-F. 1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur. <i>European Journal of Organic Chemistry</i>. 2018;2018(10):1274-1276. doi:<a href=\"https://doi.org/10.1002/ejoc.201701813\">10.1002/ejoc.201701813</a>","chicago":"Hu, Yuya, Zhiping Yin, Thomas Werner, Anke Spannenberg, and Xiao-Feng Wu. “1,8-Diazabicyclo[5.4.0]Undec-7-Ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur.” <i>European Journal of Organic Chemistry</i> 2018, no. 10 (2018): 1274–76. <a href=\"https://doi.org/10.1002/ejoc.201701813\">https://doi.org/10.1002/ejoc.201701813</a>.","ieee":"Y. Hu, Z. Yin, T. Werner, A. Spannenberg, and X.-F. Wu, “1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur,” <i>European Journal of Organic Chemistry</i>, vol. 2018, no. 10, pp. 1274–1276, 2018, doi: <a href=\"https://doi.org/10.1002/ejoc.201701813\">10.1002/ejoc.201701813</a>.","short":"Y. Hu, Z. Yin, T. Werner, A. Spannenberg, X.-F. Wu, European Journal of Organic Chemistry 2018 (2018) 1274–1276.","bibtex":"@article{Hu_Yin_Werner_Spannenberg_Wu_2018, title={1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur}, volume={2018}, DOI={<a href=\"https://doi.org/10.1002/ejoc.201701813\">10.1002/ejoc.201701813</a>}, number={10}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Hu, Yuya and Yin, Zhiping and Werner, Thomas and Spannenberg, Anke and Wu, Xiao-Feng}, year={2018}, pages={1274–1276} }","mla":"Hu, Yuya, et al. “1,8-Diazabicyclo[5.4.0]Undec-7-Ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur.” <i>European Journal of Organic Chemistry</i>, vol. 2018, no. 10, Wiley, 2018, pp. 1274–76, doi:<a href=\"https://doi.org/10.1002/ejoc.201701813\">10.1002/ejoc.201701813</a>.","apa":"Hu, Y., Yin, Z., Werner, T., Spannenberg, A., &#38; Wu, X.-F. (2018). 1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur. <i>European Journal of Organic Chemistry</i>, <i>2018</i>(10), 1274–1276. <a href=\"https://doi.org/10.1002/ejoc.201701813\">https://doi.org/10.1002/ejoc.201701813</a>"},"intvolume":"      2018","page":"1274-1276","publication_status":"published","publication_identifier":{"issn":["1434-193X"]},"doi":"10.1002/ejoc.201701813","date_updated":"2025-11-10T09:05:47Z","author":[{"full_name":"Hu, Yuya","last_name":"Hu","first_name":"Yuya"},{"first_name":"Zhiping","full_name":"Yin, Zhiping","last_name":"Yin"},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner"},{"first_name":"Anke","last_name":"Spannenberg","full_name":"Spannenberg, Anke"},{"first_name":"Xiao-Feng","full_name":"Wu, Xiao-Feng","last_name":"Wu"}],"volume":2018,"status":"public","type":"journal_article","alternative_title":["1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur"],"extern":"1","_id":"37968","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"year":"2018","issue":"10","title":"1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur","publisher":"Wiley","date_created":"2023-01-22T20:46:32Z","publication":"European Journal of Organic Chemistry","keyword":["Organic Chemistry","Physical and Theoretical Chemistry"],"language":[{"iso":"eng"}]},{"volume":6,"author":[{"first_name":"Johannes","last_name":"Steinbauer","full_name":"Steinbauer, Johannes"},{"last_name":"Kubis","full_name":"Kubis, Christoph","first_name":"Christoph"},{"last_name":"Ludwig","full_name":"Ludwig, Ralf","first_name":"Ralf"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"date_updated":"2025-11-10T09:04:50Z","doi":"10.1021/acssuschemeng.8b02093","publication_identifier":{"issn":["2168-0485","2168-0485"]},"publication_status":"published","intvolume":"         6","page":"10778-10788","citation":{"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>.","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>.","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>","short":"J. Steinbauer, C. Kubis, R. Ludwig, T. Werner, ACS Sustainable Chemistry and Engineering 6 (2018) 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>.","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} }","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>"},"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37967","extern":"1","type":"journal_article","status":"public","date_created":"2023-01-22T20:46:04Z","publisher":"American Chemical Society (ACS)","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","issue":"8","year":"2018","language":[{"iso":"eng"}],"keyword":["T1","T2","CSSD"],"publication":"ACS Sustainable Chemistry and Engineering"},{"type":"journal_article","publication":"RSC Advances","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>"}],"user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37969","language":[{"iso":"eng"}],"extern":"1","keyword":["T1","T3","CSSD"],"issue":"7","publication_status":"published","publication_identifier":{"issn":["2046-2069"]},"citation":{"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>","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>.","short":"C. Wulf, U. Doering, T. Werner, RSC Advances 8 (2018) 3673–3679.","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} }","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>.","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>.","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>"},"intvolume":"         8","page":"3673-3679","year":"2018","author":[{"last_name":"Wulf","full_name":"Wulf, Christoph","first_name":"Christoph"},{"first_name":"Ulrike","last_name":"Doering","full_name":"Doering, Ulrike"},{"last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"date_created":"2023-01-22T20:46:56Z","volume":8,"publisher":"Royal Society of Chemistry (RSC)","date_updated":"2025-11-10T09:03:07Z","doi":"10.1039/c7ra12535f","title":"Copolymerization of CO<sub>2</sub> and epoxides mediated by zinc organyls"},{"date_updated":"2025-11-10T09:05:26Z","volume":8,"author":[{"first_name":"Lars","full_name":"Longwitz, Lars","last_name":"Longwitz"},{"last_name":"Steinbauer","full_name":"Steinbauer, Johannes","first_name":"Johannes"},{"last_name":"Spannenberg","full_name":"Spannenberg, Anke","first_name":"Anke"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271","full_name":"Werner, Thomas"}],"doi":"10.1021/acscatal.7b03367","publication_identifier":{"issn":["2155-5435","2155-5435"]},"publication_status":"published","page":"665-672","intvolume":"         8","citation":{"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>.","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>.","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>","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>","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."},"_id":"62105","department":[{"_id":"35"},{"_id":"2"}],"user_id":"89271","type":"journal_article","status":"public","publisher":"American Chemical Society (ACS)","date_created":"2025-11-05T15:47:56Z","title":"Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions","issue":"1","year":"2018","keyword":["T1","T3","T4","CSSD"],"language":[{"iso":"eng"}],"publication":"ACS Catalysis"},{"type":"journal_article","status":"public","_id":"37970","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","extern":"1","publication_identifier":{"issn":["2155-5435","2155-5435"]},"publication_status":"published","page":"665-672","intvolume":"         8","citation":{"bibtex":"@article{Longwitz_Steinbauer_Spannenberg_Werner_2017, 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={2017}, pages={665–672} }","short":"L. Longwitz, J. Steinbauer, A. Spannenberg, T. Werner, ACS Catalysis 8 (2017) 665–672.","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), 2017, pp. 665–72, doi:<a href=\"https://doi.org/10.1021/acscatal.7b03367\">10.1021/acscatal.7b03367</a>.","apa":"Longwitz, L., Steinbauer, J., Spannenberg, A., &#38; Werner, T. (2017). 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>. 2017;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 (2017): 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, 2017, doi: <a href=\"https://doi.org/10.1021/acscatal.7b03367\">10.1021/acscatal.7b03367</a>."},"date_updated":"2025-11-06T08:38:07Z","volume":8,"author":[{"full_name":"Longwitz, Lars","last_name":"Longwitz","first_name":"Lars"},{"full_name":"Steinbauer, Johannes","last_name":"Steinbauer","first_name":"Johannes"},{"last_name":"Spannenberg","full_name":"Spannenberg, Anke","first_name":"Anke"},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","orcid":"https://orcid.org/0000-0001-9025-3244","last_name":"Werner"}],"doi":"10.1021/acscatal.7b03367","publication":"ACS Catalysis","keyword":["T1","T3","T4"],"language":[{"iso":"eng"}],"issue":"1","year":"2017","publisher":"American Chemical Society (ACS)","date_created":"2023-01-22T20:47:19Z","title":"Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions"},{"type":"journal_article","status":"public","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"},{"_id":"389"}],"_id":"37979","extern":"1","publication_status":"published","publication_identifier":{"issn":["1439-9598"]},"citation":{"apa":"Straub, B. 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>","bibtex":"@article{Straub_Andexer_Arenz_Beifuss_Beuerle_Brasholz_Breinbauer_Ditrich_Gulder_Hüttel_et al._2017, title={Organische Chemie 2016}, volume={65}, DOI={<a href=\"https://doi.org/10.1002/nadc.20174059831\">10.1002/nadc.20174059831</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Straub, Bernd F. and Andexer, Jennifer and Arenz, Christoph and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ditrich, Klaus and Gulder, Tobias A. M. and Hüttel, Wolfgang and et al.}, year={2017}, pages={266–304} }","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. Worgull, Nachrichten Aus Der Chemie 65 (2017) 266–304.","mla":"Straub, Bernd F., et al. “Organische Chemie 2016.” <i>Nachrichten Aus Der Chemie</i>, vol. 65, no. 3, Wiley, 2017, pp. 266–304, doi:<a href=\"https://doi.org/10.1002/nadc.20174059831\">10.1002/nadc.20174059831</a>.","ama":"Straub BF, Andexer J, Arenz C, et al. 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. Straub <i>et al.</i>, “Organische Chemie 2016,” <i>Nachrichten aus der Chemie</i>, vol. 65, no. 3, pp. 266–304, 2017, doi: <a href=\"https://doi.org/10.1002/nadc.20174059831\">10.1002/nadc.20174059831</a>.","chicago":"Straub, Bernd F., Jennifer Andexer, Christoph Arenz, Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, et al. “Organische Chemie 2016.” <i>Nachrichten Aus Der Chemie</i> 65, no. 3 (2017): 266–304. <a href=\"https://doi.org/10.1002/nadc.20174059831\">https://doi.org/10.1002/nadc.20174059831</a>."},"page":"266-304","intvolume":"        65","author":[{"first_name":"Bernd F.","full_name":"Straub, Bernd F.","last_name":"Straub"},{"first_name":"Jennifer","full_name":"Andexer, Jennifer","last_name":"Andexer"},{"last_name":"Arenz","full_name":"Arenz, Christoph","first_name":"Christoph"},{"full_name":"Beifuss, Uwe","last_name":"Beifuss","first_name":"Uwe"},{"full_name":"Beuerle, Florian","last_name":"Beuerle","first_name":"Florian"},{"first_name":"Malte","last_name":"Brasholz","full_name":"Brasholz, Malte"},{"full_name":"Breinbauer, Rolf","last_name":"Breinbauer","first_name":"Rolf"},{"first_name":"Klaus","full_name":"Ditrich, Klaus","last_name":"Ditrich"},{"first_name":"Tobias A. M.","last_name":"Gulder","full_name":"Gulder, Tobias A. M."},{"first_name":"Wolfgang","last_name":"Hüttel","full_name":"Hüttel, Wolfgang"},{"last_name":"Kordes","full_name":"Kordes, Markus","first_name":"Markus"},{"last_name":"Krueger","full_name":"Krueger, Anke","first_name":"Anke"},{"first_name":"Matthias","full_name":"Lehmann, Matthias","last_name":"Lehmann"},{"last_name":"Lindel","full_name":"Lindel, Thomas","first_name":"Thomas"},{"full_name":"Luy, Burkhard","last_name":"Luy","first_name":"Burkhard"},{"first_name":"Michael A. R.","full_name":"Meier, Michael A. R.","last_name":"Meier"},{"first_name":"Christian","last_name":"Mück-Lichtenfeld","full_name":"Mück-Lichtenfeld, Christian"},{"first_name":"Claudia","last_name":"Muhle-Goll","full_name":"Muhle-Goll, Claudia"},{"last_name":"Müller","full_name":"Müller, Thomas J. J.","first_name":"Thomas J. J."},{"first_name":"Arun","last_name":"Narine","full_name":"Narine, Arun"},{"id":"53339","full_name":"Paradies, Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies","first_name":"Jan"},{"first_name":"Roland","full_name":"Pfau, Roland","last_name":"Pfau"},{"last_name":"Pietruszka","full_name":"Pietruszka, Jörg","first_name":"Jörg"},{"full_name":"Schaschke, Norbert","last_name":"Schaschke","first_name":"Norbert"},{"last_name":"Senge","full_name":"Senge, Mathias O.","first_name":"Mathias O."},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"},{"full_name":"Werz, Daniel B.","last_name":"Werz","first_name":"Daniel B."},{"first_name":"Christian A.","full_name":"Winter, Christian A.","last_name":"Winter"},{"first_name":"Dennis","full_name":"Worgull, Dennis","last_name":"Worgull"}],"volume":65,"date_updated":"2025-11-10T09:11:28Z","doi":"10.1002/nadc.20174059831","publication":"Nachrichten aus der Chemie","language":[{"iso":"eng"}],"keyword":["General Chemical Engineering","General Chemistry"],"issue":"3","year":"2017","date_created":"2023-01-22T21:00:37Z","publisher":"Wiley","title":"Organische Chemie 2016"},{"status":"public","type":"journal_article","extern":"1","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37976","page":"2568-2571","intvolume":"        19","citation":{"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>","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>.","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.","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} }","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>."},"publication_identifier":{"issn":["1523-7060","1523-7052"]},"publication_status":"published","doi":"10.1021/acs.orglett.7b00720","volume":19,"author":[{"full_name":"Li, Wu","last_name":"Li","first_name":"Wu"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas"}],"date_updated":"2025-11-10T09:14:45Z","publication":"Organic Letters","language":[{"iso":"eng"}],"keyword":["CSSD"],"year":"2017","issue":"10","title":"B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles","date_created":"2023-01-22T20:59:34Z","publisher":"American Chemical Society (ACS)"},{"year":"2017","page":"4435-4445","intvolume":"        19","citation":{"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} }","short":"J. Steinbauer, L. Longwitz, M. Frank, J. Epping, U. Kragl, T. Werner, Green Chemistry 19 (2017) 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>","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>","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>.","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>."},"publication_identifier":{"issn":["1463-9262","1463-9270"]},"publication_status":"published","issue":"18","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,"author":[{"last_name":"Steinbauer","full_name":"Steinbauer, J.","first_name":"J."},{"first_name":"L.","last_name":"Longwitz","full_name":"Longwitz, L."},{"last_name":"Frank","full_name":"Frank, M.","first_name":"M."},{"first_name":"J.","full_name":"Epping, J.","last_name":"Epping"},{"first_name":"U.","full_name":"Kragl, U.","last_name":"Kragl"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"date_created":"2023-01-22T20:57:38Z","abstract":[{"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>","lang":"eng"}],"status":"public","publication":"Green Chemistry","type":"journal_article","keyword":["T1","T2","CSSD"],"extern":"1","language":[{"iso":"eng"}],"_id":"37973","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271"},{"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"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"date_created":"2023-01-22T20:59:12Z","date_updated":"2025-11-10T09:18:18Z","publisher":"Royal Society of Chemistry (RSC)","page":"3769-3779","intvolume":"        19","citation":{"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>.","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>.","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>","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} }","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>.","short":"J. Steinbauer, A. Spannenberg, T. Werner, Green Chemistry 19 (2017) 3769–3779.","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>"},"year":"2017","issue":"16","publication_identifier":{"issn":["1463-9262","1463-9270"]},"publication_status":"published","language":[{"iso":"eng"}],"extern":"1","keyword":["T1","T3","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37975","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"},{"status":"public","type":"journal_article","publication":"Topics in Current Chemistry","article_number":"50","keyword":["T1","CSSD"],"language":[{"iso":"eng"}],"extern":"1","_id":"37977","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"year":"2017","citation":{"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>.","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. 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>","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} }"},"intvolume":"       375","publication_status":"published","publication_identifier":{"issn":["2365-0869","2364-8961"]},"issue":"3","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","date_created":"2023-01-22T20:59:56Z","author":[{"first_name":"Hendrik","last_name":"Büttner","full_name":"Büttner, Hendrik"},{"full_name":"Longwitz, Lars","last_name":"Longwitz","first_name":"Lars"},{"full_name":"Steinbauer, Johannes","last_name":"Steinbauer","first_name":"Johannes"},{"full_name":"Wulf, Christoph","last_name":"Wulf","first_name":"Christoph"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas"}],"volume":375},{"publisher":"American Chemical Society (ACS)","date_updated":"2025-11-10T09:18:33Z","author":[{"full_name":"Li, Wu","last_name":"Li","first_name":"Wu"},{"last_name":"Wang","full_name":"Wang, Ming-Ming","first_name":"Ming-Ming"},{"last_name":"Hu","full_name":"Hu, Yuya","first_name":"Yuya"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"date_created":"2023-01-22T20:57:15Z","volume":19,"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","publication_status":"published","publication_identifier":{"issn":["1523-7060","1523-7052"]},"issue":"21","year":"2017","citation":{"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>.","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>.","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>","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","_id":"37972","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["CSSD"],"extern":"1","language":[{"iso":"eng"}],"type":"journal_article","publication":"Organic Letters","status":"public"},{"publication":"ChemSusChem","language":[{"iso":"eng"}],"keyword":["T1","T2","CSSD"],"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","type":"journal_article","status":"public","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37978","extern":"1","publication_status":"published","publication_identifier":{"issn":["1864-5631"]},"citation":{"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} }","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>.","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>","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>"},"page":"1076-1079","intvolume":"        10","author":[{"first_name":"Hendrik","full_name":"Büttner, Hendrik","last_name":"Büttner"},{"first_name":"Johannes","full_name":"Steinbauer, Johannes","last_name":"Steinbauer"},{"full_name":"Wulf, Christoph","last_name":"Wulf","first_name":"Christoph"},{"last_name":"Dindaroglu","full_name":"Dindaroglu, Mehmet","first_name":"Mehmet"},{"first_name":"Hans-Günther","full_name":"Schmalz, Hans-Günther","last_name":"Schmalz"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas"}],"volume":10,"date_updated":"2025-11-10T09:17:59Z","doi":"10.1002/cssc.201601163"},{"date_created":"2023-01-22T20:58:02Z","publisher":"Wiley","title":"Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis","issue":"15","year":"2017","language":[{"iso":"eng"}],"keyword":["T1","T3","CSSD"],"publication":"ChemSusChem","author":[{"last_name":"Steinbauer","full_name":"Steinbauer, Johannes","first_name":"Johannes"},{"orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"volume":10,"date_updated":"2025-11-10T09:17:48Z","doi":"10.1002/cssc.201700788","publication_status":"published","publication_identifier":{"issn":["1864-5631"]},"citation":{"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>","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>.","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>.","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>"},"page":"3025-3029","intvolume":"        10","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37974","extern":"1","type":"journal_article","status":"public"},{"year":"2016","issue":"13","title":"Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables","date_created":"2023-01-22T21:03:02Z","publisher":"Royal Society of Chemistry (RSC)","abstract":[{"lang":"eng","text":"<p><bold>Taking Control!</bold>The binary catalyst system composed of MoO<sub>3</sub>and an organic phoshponium salt [Bu<sub>4</sub>P]X proved very efficient to produce oleochemical cyclic carbonates from renewables.</p>"}],"publication":"Green Chemistry","language":[{"iso":"eng"}],"keyword":["T1","T3","CSSD"],"citation":{"bibtex":"@article{Tenhumberg_Büttner_Schäffner_Kruse_Blumenstein_Werner_2016, title={Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables}, volume={18}, DOI={<a href=\"https://doi.org/10.1039/c6gc00671j\">10.1039/c6gc00671j</a>}, number={13}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Tenhumberg, Nils and Büttner, Hendrik and Schäffner, Benjamin and Kruse, Daniela and Blumenstein, Michael and Werner, Thomas}, year={2016}, pages={3775–3788} }","short":"N. Tenhumberg, H. Büttner, B. Schäffner, D. Kruse, M. Blumenstein, T. Werner, Green Chemistry 18 (2016) 3775–3788.","mla":"Tenhumberg, Nils, et al. “Cooperative Catalyst System for the Synthesis of Oleochemical Cyclic Carbonates from CO<sub>2</sub>and Renewables.” <i>Green Chemistry</i>, vol. 18, no. 13, Royal Society of Chemistry (RSC), 2016, pp. 3775–88, doi:<a href=\"https://doi.org/10.1039/c6gc00671j\">10.1039/c6gc00671j</a>.","apa":"Tenhumberg, N., Büttner, H., Schäffner, B., Kruse, D., Blumenstein, M., &#38; Werner, T. (2016). Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables. <i>Green Chemistry</i>, <i>18</i>(13), 3775–3788. <a href=\"https://doi.org/10.1039/c6gc00671j\">https://doi.org/10.1039/c6gc00671j</a>","ieee":"N. Tenhumberg, H. Büttner, B. Schäffner, D. Kruse, M. Blumenstein, and T. Werner, “Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables,” <i>Green Chemistry</i>, vol. 18, no. 13, pp. 3775–3788, 2016, doi: <a href=\"https://doi.org/10.1039/c6gc00671j\">10.1039/c6gc00671j</a>.","chicago":"Tenhumberg, Nils, Hendrik Büttner, Benjamin Schäffner, Daniela Kruse, Michael Blumenstein, and Thomas Werner. “Cooperative Catalyst System for the Synthesis of Oleochemical Cyclic Carbonates from CO<sub>2</sub>and Renewables.” <i>Green Chemistry</i> 18, no. 13 (2016): 3775–88. <a href=\"https://doi.org/10.1039/c6gc00671j\">https://doi.org/10.1039/c6gc00671j</a>.","ama":"Tenhumberg N, Büttner H, Schäffner B, Kruse D, Blumenstein M, Werner T. Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables. <i>Green Chemistry</i>. 2016;18(13):3775-3788. doi:<a href=\"https://doi.org/10.1039/c6gc00671j\">10.1039/c6gc00671j</a>"},"intvolume":"        18","page":"3775-3788","publication_status":"published","publication_identifier":{"issn":["1463-9262","1463-9270"]},"doi":"10.1039/c6gc00671j","author":[{"first_name":"Nils","last_name":"Tenhumberg","full_name":"Tenhumberg, Nils"},{"first_name":"Hendrik","last_name":"Büttner","full_name":"Büttner, Hendrik"},{"full_name":"Schäffner, Benjamin","last_name":"Schäffner","first_name":"Benjamin"},{"full_name":"Kruse, Daniela","last_name":"Kruse","first_name":"Daniela"},{"last_name":"Blumenstein","full_name":"Blumenstein, Michael","first_name":"Michael"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"volume":18,"date_updated":"2025-11-10T09:20:35Z","status":"public","type":"journal_article","extern":"1","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37983"},{"intvolume":"       358","page":"26-29","citation":{"short":"M.-L. Schirmer, S. Jopp, J. Holz, A. Spannenberg, T. Werner, Advanced Synthesis and Catalysis 358 (2016) 26–29.","bibtex":"@article{Schirmer_Jopp_Holz_Spannenberg_Werner_2016, title={Organocatalyzed Reduction of Tertiary Phosphine Oxides}, volume={358}, DOI={<a href=\"https://doi.org/10.1002/adsc.201500762\">10.1002/adsc.201500762</a>}, number={1}, journal={Advanced Synthesis and Catalysis}, publisher={Wiley}, author={Schirmer, Marie-Luis and Jopp, Stefan and Holz, Jens and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={26–29} }","mla":"Schirmer, Marie-Luis, et al. “Organocatalyzed Reduction of Tertiary Phosphine Oxides.” <i>Advanced Synthesis and Catalysis</i>, vol. 358, no. 1, Wiley, 2016, pp. 26–29, doi:<a href=\"https://doi.org/10.1002/adsc.201500762\">10.1002/adsc.201500762</a>.","apa":"Schirmer, M.-L., Jopp, S., Holz, J., Spannenberg, A., &#38; Werner, T. (2016). Organocatalyzed Reduction of Tertiary Phosphine Oxides. <i>Advanced Synthesis and Catalysis</i>, <i>358</i>(1), 26–29. <a href=\"https://doi.org/10.1002/adsc.201500762\">https://doi.org/10.1002/adsc.201500762</a>","ieee":"M.-L. Schirmer, S. Jopp, J. Holz, A. Spannenberg, and T. Werner, “Organocatalyzed Reduction of Tertiary Phosphine Oxides,” <i>Advanced Synthesis and Catalysis</i>, vol. 358, no. 1, pp. 26–29, 2016, doi: <a href=\"https://doi.org/10.1002/adsc.201500762\">10.1002/adsc.201500762</a>.","chicago":"Schirmer, Marie-Luis, Stefan Jopp, Jens Holz, Anke Spannenberg, and Thomas Werner. “Organocatalyzed Reduction of Tertiary Phosphine Oxides.” <i>Advanced Synthesis and Catalysis</i> 358, no. 1 (2016): 26–29. <a href=\"https://doi.org/10.1002/adsc.201500762\">https://doi.org/10.1002/adsc.201500762</a>.","ama":"Schirmer M-L, Jopp S, Holz J, Spannenberg A, Werner T. Organocatalyzed Reduction of Tertiary Phosphine Oxides. <i>Advanced Synthesis and Catalysis</i>. 2016;358(1):26-29. doi:<a href=\"https://doi.org/10.1002/adsc.201500762\">10.1002/adsc.201500762</a>"},"year":"2016","issue":"1","publication_identifier":{"issn":["1615-4150"]},"publication_status":"published","doi":"10.1002/adsc.201500762","title":"Organocatalyzed Reduction of Tertiary Phosphine Oxides","volume":358,"date_created":"2023-01-22T21:05:14Z","author":[{"full_name":"Schirmer, Marie-Luis","last_name":"Schirmer","first_name":"Marie-Luis"},{"first_name":"Stefan","full_name":"Jopp, Stefan","last_name":"Jopp"},{"first_name":"Jens","full_name":"Holz, Jens","last_name":"Holz"},{"last_name":"Spannenberg","full_name":"Spannenberg, Anke","first_name":"Anke"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"publisher":"Wiley","date_updated":"2025-11-10T09:22:07Z","status":"public","publication":"Advanced Synthesis and Catalysis","type":"journal_article","extern":"1","language":[{"iso":"eng"}],"keyword":["T2","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37989"},{"doi":"10.1107/s2053229616008159","author":[{"first_name":"Marie-Luis","full_name":"Schirmer, Marie-Luis","last_name":"Schirmer"},{"full_name":"Spannenberg, Anke","last_name":"Spannenberg","first_name":"Anke"},{"full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"volume":72,"date_updated":"2025-11-10T09:23:46Z","citation":{"mla":"Schirmer, Marie-Luis, et al. “Highly Functionalized Alkenes Produced from Base-Free Organocatalytic Wittig Reactions: (<i>E</i>)-3-Benzylidenepyrrolidine-2,5-Dione, (<i>E</i>)-3-Benzylidene-1-Methylpyrrolidine-2,5-Dione and (<i>E</i>)-3-Benzylidene-1-<i>Tert</i>-Butylpyrrolidine-2,5-Dione.” <i>Acta Crystallographica Section C Structural Chemistry</i>, vol. 72, no. 6, International Union of Crystallography (IUCr), 2016, pp. 504–08, doi:<a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>.","bibtex":"@article{Schirmer_Spannenberg_Werner_2016, title={Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione}, volume={72}, DOI={<a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>}, number={6}, journal={Acta Crystallographica Section C Structural Chemistry}, publisher={International Union of Crystallography (IUCr)}, author={Schirmer, Marie-Luis and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={504–508} }","short":"M.-L. Schirmer, A. Spannenberg, T. Werner, Acta Crystallographica Section C Structural Chemistry 72 (2016) 504–508.","apa":"Schirmer, M.-L., Spannenberg, A., &#38; Werner, T. (2016). Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione. <i>Acta Crystallographica Section C Structural Chemistry</i>, <i>72</i>(6), 504–508. <a href=\"https://doi.org/10.1107/s2053229616008159\">https://doi.org/10.1107/s2053229616008159</a>","ama":"Schirmer M-L, Spannenberg A, Werner T. Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione. <i>Acta Crystallographica Section C Structural Chemistry</i>. 2016;72(6):504-508. doi:<a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>","ieee":"M.-L. Schirmer, A. Spannenberg, and T. Werner, “Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione,” <i>Acta Crystallographica Section C Structural Chemistry</i>, vol. 72, no. 6, pp. 504–508, 2016, doi: <a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>.","chicago":"Schirmer, Marie-Luis, Anke Spannenberg, and Thomas Werner. “Highly Functionalized Alkenes Produced from Base-Free Organocatalytic Wittig Reactions: (<i>E</i>)-3-Benzylidenepyrrolidine-2,5-Dione, (<i>E</i>)-3-Benzylidene-1-Methylpyrrolidine-2,5-Dione and (<i>E</i>)-3-Benzylidene-1-<i>Tert</i>-Butylpyrrolidine-2,5-Dione.” <i>Acta Crystallographica Section C Structural Chemistry</i> 72, no. 6 (2016): 504–8. <a href=\"https://doi.org/10.1107/s2053229616008159\">https://doi.org/10.1107/s2053229616008159</a>."},"intvolume":"        72","page":"504-508","publication_status":"published","publication_identifier":{"issn":["2053-2296"]},"extern":"1","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37984","status":"public","type":"journal_article","title":"Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione","date_created":"2023-01-22T21:03:23Z","publisher":"International Union of Crystallography (IUCr)","year":"2016","issue":"6","language":[{"iso":"eng"}],"keyword":["T2"],"abstract":[{"lang":"eng","text":"<jats:p>The Wittig reaction is a fundamental transformation for the preparation of alkenes from carbonyl compounds and phosphonium ylides. The ylides are prepared prior to the olefination step from the respective phosphonium salts by deprotonation utilizing strong bases. A first free-base catalytic Wittig reaction for the preparation of highly functionalized alkenes was based on tributylphosphane as the catalyst. Subsequently we developed a system employing a phospholene oxide as a pre-catalyst and trimethoxysilane as reducing agent which operates under milder conditions. The title compounds, (<jats:italic>E</jats:italic>)-3-benzylidenepyrrolidine-2,5-dione, C<jats:sub>11</jats:sub>H<jats:sub>9</jats:sub>NO<jats:sub>2</jats:sub>, (I), the methylpyrrolidine derivative, C<jats:sub>12</jats:sub>H<jats:sub>11</jats:sub>NO<jats:sub>2</jats:sub>, (II), and the<jats:italic>tert-</jats:italic>butylpyrrolidine derivative, C<jats:sub>15</jats:sub>H<jats:sub>17</jats:sub>NO<jats:sub>2</jats:sub>, (III), have been synthesized by base-free catalytic Wittig reactions. In the crystal of (I), molecules are linked into centrosymmetric dimers<jats:italic>via</jats:italic>pairs of N—H...O hydrogen bonds. Furthermore, in the crystal structure of (III), there are two molecules in the asymmetric unit, whereas in (I) and (II), only one molecule is present.</jats:p>"}],"publication":"Acta Crystallographica Section C Structural Chemistry"}]