[{"citation":{"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>.","short":"L. Longwitz, S. Jopp, T. Werner, The Journal of Organic Chemistry 84 (2019) 7863–7870.","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>","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>.","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>","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} }","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>."},"status":"public","volume":84,"user_id":"89271","_id":"37962","publisher":"American Chemical Society (ACS)","page":"7863-7870","extern":"1","issue":"12","publication":"The Journal of Organic Chemistry","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2","CSSD"],"type":"journal_article","date_created":"2023-01-22T20:44:02Z","intvolume":"        84","date_updated":"2025-11-10T08:54:28Z","publication_status":"published","publication_identifier":{"issn":["0022-3263","1520-6904"]},"author":[{"first_name":"Lars","last_name":"Longwitz","full_name":"Longwitz, Lars"},{"last_name":"Jopp","first_name":"Stefan","full_name":"Jopp, Stefan"},{"id":"89271","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas"}],"title":"Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling","year":"2019","doi":"10.1021/acs.joc.9b00741","language":[{"iso":"eng"}]},{"date_updated":"2025-11-10T09:01:38Z","publication_status":"published","intvolume":"       365","year":"2019","title":"The Mitsunobu reaction, reimagined","author":[{"last_name":"Longwitz","first_name":"Lars","full_name":"Longwitz, Lars"},{"id":"89271","last_name":"Werner","first_name":"Thomas","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas"}],"publication_identifier":{"issn":["0036-8075","1095-9203"]},"doi":"10.1126/science.aay6635","language":[{"iso":"eng"}],"abstract":[{"lang":"eng","text":"<jats:p>Catalytic nucleophilic substitution of alcohols makes organic synthesis greener</jats:p>"}],"issue":"6456","publication":"Science","keyword":["T2","CSSD"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T20:42:20Z","status":"public","user_id":"89271","volume":365,"page":"866-867","_id":"37959","publisher":"American Association for the Advancement of Science (AAAS)","citation":{"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} }","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>","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>.","short":"L. Longwitz, T. Werner, Science 365 (2019) 866–867.","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>.","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>"}},{"date_created":"2023-01-22T20:42:48Z","type":"journal_article","keyword":["T4","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"issue":"9","publication":"ACS Catalysis","language":[{"iso":"eng"}],"doi":"10.1021/acscatal.9b01665","year":"2019","title":"Catalytic Approaches to Monomers for Polymers Based on Renewables","publication_identifier":{"issn":["2155-5435","2155-5435"]},"author":[{"full_name":"Stadler, Bernhard M.","last_name":"Stadler","first_name":"Bernhard M."},{"full_name":"Wulf, Christoph","first_name":"Christoph","last_name":"Wulf"},{"id":"89271","first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas"},{"full_name":"Tin, Sergey","first_name":"Sergey","last_name":"Tin"},{"first_name":"Johannes G.","last_name":"de Vries","full_name":"de Vries, Johannes G."}],"date_updated":"2025-11-10T09:01:51Z","publication_status":"published","intvolume":"         9","citation":{"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} }","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>","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>.","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>.","short":"B.M. Stadler, C. Wulf, T. Werner, S. Tin, J.G. de Vries, ACS Catalysis 9 (2019) 8012–8067.","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>"},"page":"8012-8067","_id":"37960","publisher":"American Chemical Society (ACS)","user_id":"89271","volume":9,"status":"public"},{"citation":{"short":"L. Longwitz, T. Werner, Pure and Applied Chemistry 91 (2019) 95–102.","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>.","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>","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} }","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>","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>."},"volume":91,"user_id":"89271","publisher":"Walter de Gruyter GmbH","_id":"37966","page":"95-102","status":"public","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2","CSSD"],"type":"journal_article","date_created":"2023-01-22T20:45:38Z","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"}],"extern":"1","publication":"Pure and Applied Chemistry","issue":"1","doi":"10.1515/pac-2018-0920","language":[{"iso":"eng"}],"intvolume":"        91","date_updated":"2025-11-10T09:06:58Z","publication_status":"published","publication_identifier":{"issn":["1365-3075","0033-4545"]},"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"}],"title":"Recent advances in catalytic Wittig-type reactions based on P(III)/P(V) redox cycling","year":"2019"},{"date_created":"2023-01-22T20:45:12Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T2","T4","CSSD"],"publication":"The Journal of Organic Chemistry","issue":"3","extern":"1","language":[{"iso":"eng"}],"doi":"10.1021/acs.joc.8b02789","publication_identifier":{"issn":["0022-3263","1520-6904"]},"author":[{"last_name":"Grandane","first_name":"Aiga","full_name":"Grandane, Aiga"},{"full_name":"Longwitz, Lars","last_name":"Longwitz","first_name":"Lars"},{"last_name":"Roolf","first_name":"Catrin","full_name":"Roolf, Catrin"},{"first_name":"Anke","last_name":"Spannenberg","full_name":"Spannenberg, Anke"},{"full_name":"Murua Escobar, Hugo","first_name":"Hugo","last_name":"Murua Escobar"},{"full_name":"Junghanss, Christian","first_name":"Christian","last_name":"Junghanss"},{"last_name":"Suna","first_name":"Edgars","full_name":"Suna, Edgars"},{"id":"89271","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas"}],"year":"2019","title":"Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones","intvolume":"        84","date_updated":"2025-11-10T09:10:18Z","publication_status":"published","citation":{"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>.","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.","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>.","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>","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} }","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>","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>."},"_id":"37965","publisher":"American Chemical Society (ACS)","page":"1320-1329","volume":84,"user_id":"89271","status":"public"},{"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"},{"_id":"389"}],"type":"journal_article","keyword":["General Chemical Engineering","General Chemistry"],"date_created":"2023-01-22T20:48:24Z","extern":"1","issue":"3","publication":"Nachrichten aus der Chemie","doi":"10.1002/nadc.20184072148","language":[{"iso":"eng"}],"intvolume":"        66","publication_status":"published","date_updated":"2025-11-10T09:03:49Z","publication_identifier":{"issn":["1439-9598"]},"author":[{"full_name":"Straub, Bernd","last_name":"Straub","first_name":"Bernd"},{"last_name":"Andexer","first_name":"Jennifer N.","full_name":"Andexer, Jennifer N."},{"full_name":"Arenz, Christoph","last_name":"Arenz","first_name":"Christoph"},{"full_name":"Beifuss, Uwe","first_name":"Uwe","last_name":"Beifuss"},{"last_name":"Beuerle","first_name":"Florian","full_name":"Beuerle, Florian"},{"full_name":"Brasholz, Malte","last_name":"Brasholz","first_name":"Malte"},{"full_name":"Breinbauer, Rolf","first_name":"Rolf","last_name":"Breinbauer"},{"full_name":"Ditrich, Klaus","last_name":"Ditrich","first_name":"Klaus"},{"full_name":"Ernst, Martin","first_name":"Martin","last_name":"Ernst"},{"first_name":"Tobias A. M.","last_name":"Gulder","full_name":"Gulder, Tobias A. M."},{"full_name":"Kordes, Markus","last_name":"Kordes","first_name":"Markus"},{"full_name":"Krueger, Anke","last_name":"Krueger","first_name":"Anke"},{"full_name":"Lehmann, Matthias","first_name":"Matthias","last_name":"Lehmann"},{"full_name":"Lindel, Thomas","first_name":"Thomas","last_name":"Lindel"},{"full_name":"Lüdeke, Steffen","first_name":"Steffen","last_name":"Lüdeke"},{"full_name":"Luy, Burkhard","first_name":"Burkhard","last_name":"Luy"},{"first_name":"Michael A. R.","last_name":"Meier","full_name":"Meier, Michael A. R."},{"full_name":"Mück-Lichtenfeld, Christian","first_name":"Christian","last_name":"Mück-Lichtenfeld"},{"first_name":"Claudia","last_name":"Muhle-Goll","full_name":"Muhle-Goll, Claudia"},{"full_name":"Narine, Arun","last_name":"Narine","first_name":"Arun"},{"id":"53339","full_name":"Paradies, Jan","orcid":"0000-0002-3698-668X","first_name":"Jan","last_name":"Paradies"},{"full_name":"Pfau, Roland","first_name":"Roland","last_name":"Pfau"},{"last_name":"Pietruszka","first_name":"Jörg","full_name":"Pietruszka, Jörg"},{"last_name":"Schaschke","first_name":"Norbert","full_name":"Schaschke, Norbert"},{"full_name":"Senge, Mathias O.","last_name":"Senge","first_name":"Mathias O."},{"id":"89271","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas"},{"first_name":"Daniel B.","last_name":"Werz","full_name":"Werz, Daniel B."},{"full_name":"Winter, Christian","last_name":"Winter","first_name":"Christian"},{"full_name":"Worgull, Dennis","last_name":"Worgull","first_name":"Dennis"}],"title":"Trendbericht Organische Chemie 2017","year":"2018","citation":{"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} }","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>","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.","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>.","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>.","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>"},"volume":66,"user_id":"89271","publisher":"Wiley","_id":"37971","page":"249-280","status":"public"},{"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["Organic Chemistry","Physical and Theoretical Chemistry"],"type":"journal_article","date_created":"2023-01-22T20:46:32Z","extern":"1","publication":"European Journal of Organic Chemistry","issue":"10","alternative_title":["1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur"],"doi":"10.1002/ejoc.201701813","language":[{"iso":"eng"}],"intvolume":"      2018","date_updated":"2025-11-10T09:05:47Z","publication_status":"published","publication_identifier":{"issn":["1434-193X"]},"author":[{"full_name":"Hu, Yuya","first_name":"Yuya","last_name":"Hu"},{"full_name":"Yin, Zhiping","first_name":"Zhiping","last_name":"Yin"},{"id":"89271","full_name":"Werner, Thomas","first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244"},{"first_name":"Anke","last_name":"Spannenberg","full_name":"Spannenberg, Anke"},{"last_name":"Wu","first_name":"Xiao-Feng","full_name":"Wu, Xiao-Feng"}],"title":"1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur","year":"2018","citation":{"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>.","short":"Y. Hu, Z. Yin, T. Werner, A. Spannenberg, X.-F. Wu, European Journal of Organic Chemistry 2018 (2018) 1274–1276.","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>.","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>","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} }","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>","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>."},"volume":2018,"user_id":"89271","publisher":"Wiley","_id":"37968","page":"1274-1276","status":"public"},{"status":"public","volume":6,"user_id":"89271","_id":"37967","publisher":"American Chemical Society (ACS)","page":"10778-10788","citation":{"short":"J. Steinbauer, C. Kubis, R. Ludwig, T. Werner, ACS Sustainable Chemistry and Engineering 6 (2018) 10778–10788.","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>.","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>","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} }","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>","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>."},"intvolume":"         6","publication_status":"published","date_updated":"2025-11-10T09:04:50Z","author":[{"full_name":"Steinbauer, Johannes","last_name":"Steinbauer","first_name":"Johannes"},{"first_name":"Christoph","last_name":"Kubis","full_name":"Kubis, Christoph"},{"full_name":"Ludwig, Ralf","last_name":"Ludwig","first_name":"Ralf"},{"full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas","id":"89271"}],"publication_identifier":{"issn":["2168-0485","2168-0485"]},"year":"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","doi":"10.1021/acssuschemeng.8b02093","language":[{"iso":"eng"}],"extern":"1","publication":"ACS Sustainable Chemistry and Engineering","issue":"8","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T1","T2","CSSD"],"date_created":"2023-01-22T20:46:04Z"},{"status":"public","volume":8,"user_id":"89271","_id":"37969","publisher":"Royal Society of Chemistry (RSC)","page":"3673-3679","citation":{"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} }","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>","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>.","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>","short":"C. Wulf, U. Doering, T. Werner, RSC Advances 8 (2018) 3673–3679.","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>."},"intvolume":"         8","date_updated":"2025-11-10T09:03:07Z","publication_status":"published","author":[{"last_name":"Wulf","first_name":"Christoph","full_name":"Wulf, Christoph"},{"full_name":"Doering, Ulrike","first_name":"Ulrike","last_name":"Doering"},{"id":"89271","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas"}],"publication_identifier":{"issn":["2046-2069"]},"year":"2018","title":"Copolymerization of CO<sub>2</sub> and epoxides mediated by zinc organyls","doi":"10.1039/c7ra12535f","language":[{"iso":"eng"}],"abstract":[{"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>","lang":"eng"}],"extern":"1","publication":"RSC Advances","issue":"7","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T1","T3","CSSD"],"date_created":"2023-01-22T20:46:56Z"},{"language":[{"iso":"eng"}],"doi":"10.1021/acscatal.7b03367","publication_identifier":{"issn":["2155-5435","2155-5435"]},"author":[{"last_name":"Longwitz","first_name":"Lars","full_name":"Longwitz, Lars"},{"full_name":"Steinbauer, Johannes","last_name":"Steinbauer","first_name":"Johannes"},{"full_name":"Spannenberg, Anke","last_name":"Spannenberg","first_name":"Anke"},{"first_name":"Thomas","last_name":"Werner","orcid":"https://orcid.org/0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"year":"2017","title":"Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions","intvolume":"         8","publication_status":"published","date_updated":"2025-11-06T08:38:07Z","date_created":"2023-01-22T20:47:19Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T1","T3","T4"],"issue":"1","publication":"ACS Catalysis","extern":"1","_id":"37970","publisher":"American Chemical Society (ACS)","page":"665-672","volume":8,"user_id":"89271","status":"public","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), 2017, pp. 665–72, doi:<a href=\"https://doi.org/10.1021/acscatal.7b03367\">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>","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} }","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>","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>.","short":"L. Longwitz, J. Steinbauer, A. Spannenberg, T. Werner, ACS Catalysis 8 (2017) 665–672.","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>."}},{"doi":"10.1002/nadc.20174059831","language":[{"iso":"eng"}],"intvolume":"        65","date_updated":"2025-11-10T09:11:28Z","publication_status":"published","author":[{"full_name":"Straub, Bernd F.","first_name":"Bernd F.","last_name":"Straub"},{"full_name":"Andexer, Jennifer","last_name":"Andexer","first_name":"Jennifer"},{"last_name":"Arenz","first_name":"Christoph","full_name":"Arenz, Christoph"},{"full_name":"Beifuss, Uwe","first_name":"Uwe","last_name":"Beifuss"},{"full_name":"Beuerle, Florian","last_name":"Beuerle","first_name":"Florian"},{"last_name":"Brasholz","first_name":"Malte","full_name":"Brasholz, Malte"},{"last_name":"Breinbauer","first_name":"Rolf","full_name":"Breinbauer, Rolf"},{"full_name":"Ditrich, Klaus","first_name":"Klaus","last_name":"Ditrich"},{"full_name":"Gulder, Tobias A. M.","last_name":"Gulder","first_name":"Tobias A. M."},{"full_name":"Hüttel, Wolfgang","first_name":"Wolfgang","last_name":"Hüttel"},{"last_name":"Kordes","first_name":"Markus","full_name":"Kordes, Markus"},{"full_name":"Krueger, Anke","last_name":"Krueger","first_name":"Anke"},{"last_name":"Lehmann","first_name":"Matthias","full_name":"Lehmann, Matthias"},{"last_name":"Lindel","first_name":"Thomas","full_name":"Lindel, Thomas"},{"first_name":"Burkhard","last_name":"Luy","full_name":"Luy, Burkhard"},{"first_name":"Michael A. R.","last_name":"Meier","full_name":"Meier, Michael A. R."},{"full_name":"Mück-Lichtenfeld, Christian","first_name":"Christian","last_name":"Mück-Lichtenfeld"},{"full_name":"Muhle-Goll, Claudia","last_name":"Muhle-Goll","first_name":"Claudia"},{"last_name":"Müller","first_name":"Thomas J. J.","full_name":"Müller, Thomas J. J."},{"full_name":"Narine, Arun","last_name":"Narine","first_name":"Arun"},{"full_name":"Paradies, Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan","id":"53339"},{"full_name":"Pfau, Roland","last_name":"Pfau","first_name":"Roland"},{"full_name":"Pietruszka, Jörg","first_name":"Jörg","last_name":"Pietruszka"},{"full_name":"Schaschke, Norbert","first_name":"Norbert","last_name":"Schaschke"},{"last_name":"Senge","first_name":"Mathias O.","full_name":"Senge, Mathias O."},{"id":"89271","first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas"},{"full_name":"Werz, Daniel B.","last_name":"Werz","first_name":"Daniel B."},{"first_name":"Christian A.","last_name":"Winter","full_name":"Winter, Christian A."},{"full_name":"Worgull, Dennis","last_name":"Worgull","first_name":"Dennis"}],"publication_identifier":{"issn":["1439-9598"]},"title":"Organische Chemie 2016","year":"2017","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"},{"_id":"389"}],"keyword":["General Chemical Engineering","General Chemistry"],"type":"journal_article","date_created":"2023-01-22T21:00:37Z","extern":"1","publication":"Nachrichten aus der Chemie","issue":"3","volume":65,"user_id":"89271","_id":"37979","publisher":"Wiley","page":"266-304","status":"public","citation":{"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>.","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} }","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>.","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>","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.","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>."}},{"status":"public","user_id":"89271","volume":19,"page":"2568-2571","_id":"37976","publisher":"American Chemical Society (ACS)","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>","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>.","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>.","short":"W. Li, T. Werner, Organic Letters 19 (2017) 2568–2571.","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>","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>."},"publication_status":"published","date_updated":"2025-11-10T09:14:45Z","intvolume":"        19","year":"2017","title":"B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles","author":[{"full_name":"Li, Wu","last_name":"Li","first_name":"Wu"},{"id":"89271","full_name":"Werner, Thomas","last_name":"Werner","first_name":"Thomas","orcid":"0000-0001-9025-3244"}],"publication_identifier":{"issn":["1523-7060","1523-7052"]},"doi":"10.1021/acs.orglett.7b00720","language":[{"iso":"eng"}],"extern":"1","issue":"10","publication":"Organic Letters","keyword":["CSSD"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T20:59:34Z"},{"year":"2017","title":"Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides","author":[{"full_name":"Steinbauer, J.","last_name":"Steinbauer","first_name":"J."},{"full_name":"Longwitz, L.","first_name":"L.","last_name":"Longwitz"},{"full_name":"Frank, M.","last_name":"Frank","first_name":"M."},{"last_name":"Epping","first_name":"J.","full_name":"Epping, J."},{"last_name":"Kragl","first_name":"U.","full_name":"Kragl, U."},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"publication_identifier":{"issn":["1463-9262","1463-9270"]},"publication_status":"published","date_updated":"2025-11-10T09:18:10Z","intvolume":"        19","language":[{"iso":"eng"}],"doi":"10.1039/c7gc01782k","publication":"Green Chemistry","issue":"18","extern":"1","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>"}],"date_created":"2023-01-22T20:57:38Z","keyword":["T1","T2","CSSD"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"status":"public","page":"4435-4445","_id":"37973","publisher":"Royal Society of Chemistry (RSC)","user_id":"89271","volume":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} }","ama":"Steinbauer J, Longwitz L, Frank M, Epping J, Kragl U, Werner T. 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Frank, J. Epping, U. Kragl, T. Werner, Green Chemistry 19 (2017) 4435–4445.","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>."}},{"volume":19,"user_id":"89271","publisher":"Royal Society of Chemistry (RSC)","_id":"37975","page":"3769-3779","status":"public","citation":{"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} }","chicago":"Steinbauer, J., A. 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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>"},"doi":"10.1039/c7gc01114h","language":[{"iso":"eng"}],"intvolume":"        19","publication_status":"published","date_updated":"2025-11-10T09:18:18Z","publication_identifier":{"issn":["1463-9262","1463-9270"]},"author":[{"first_name":"J.","last_name":"Steinbauer","full_name":"Steinbauer, J."},{"first_name":"A.","last_name":"Spannenberg","full_name":"Spannenberg, A."},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"year":"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","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T1","T3","CSSD"],"type":"journal_article","date_created":"2023-01-22T20:59:12Z","extern":"1","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","issue":"16"},{"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>.","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. 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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>","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} }","ama":"Büttner H, Steinbauer J, Wulf C, Dindaroglu M, Schmalz H-G, Werner T. Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables. <i>ChemSusChem</i>. 2017;10(6):1076-1079. doi:<a href=\"https://doi.org/10.1002/cssc.201601163\">10.1002/cssc.201601163</a>","mla":"Büttner, Hendrik, et al. “Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables.” <i>ChemSusChem</i>, vol. 10, no. 6, Wiley, 2017, pp. 1076–79, doi:<a href=\"https://doi.org/10.1002/cssc.201601163\">10.1002/cssc.201601163</a>."},"title":"Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables","year":"2017","publication_identifier":{"issn":["1864-5631"]},"author":[{"last_name":"Büttner","first_name":"Hendrik","full_name":"Büttner, Hendrik"},{"last_name":"Steinbauer","first_name":"Johannes","full_name":"Steinbauer, Johannes"},{"full_name":"Wulf, Christoph","first_name":"Christoph","last_name":"Wulf"},{"first_name":"Mehmet","last_name":"Dindaroglu","full_name":"Dindaroglu, Mehmet"},{"full_name":"Schmalz, Hans-Günther","first_name":"Hans-Günther","last_name":"Schmalz"},{"last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas","full_name":"Werner, Thomas","id":"89271"}],"date_updated":"2025-11-10T09:17:59Z","publication_status":"published","intvolume":"        10","language":[{"iso":"eng"}],"doi":"10.1002/cssc.201601163","publication":"ChemSusChem","issue":"6","extern":"1","date_created":"2023-01-22T21:00:17Z","keyword":["T1","T2","CSSD"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}]},{"_id":"37974","publisher":"Wiley","page":"3025-3029","volume":10,"user_id":"89271","status":"public","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>.","apa":"Steinbauer, J., &#38; Werner, T. 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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>."}},{"extern":"1","publication":"Advanced Synthesis and Catalysis","issue":"1","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T2","CSSD"],"date_created":"2023-01-22T21:05:14Z","intvolume":"       358","date_updated":"2025-11-10T09:22:07Z","publication_status":"published","author":[{"first_name":"Marie-Luis","last_name":"Schirmer","full_name":"Schirmer, Marie-Luis"},{"full_name":"Jopp, Stefan","last_name":"Jopp","first_name":"Stefan"},{"full_name":"Holz, Jens","last_name":"Holz","first_name":"Jens"},{"last_name":"Spannenberg","first_name":"Anke","full_name":"Spannenberg, Anke"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner"}],"publication_identifier":{"issn":["1615-4150"]},"year":"2016","title":"Organocatalyzed Reduction of Tertiary Phosphine Oxides","doi":"10.1002/adsc.201500762","language":[{"iso":"eng"}],"citation":{"apa":"Schirmer, M.-L., Jopp, S., Holz, J., Spannenberg, A., &#38; Werner, T. 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