[{"status":"public","abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>Highlights von November 2023 bis 2024: die erste Einelektron‐C–C‐σ‐Bindung und Anti‐Bredt‐Verbindung; gesättigte Heterocyclen elektrochemisch funktionalisieren; Ausrichten diskotischer Flüssigkristalle; enantioselektive Wagner‐Meerwein‐Umlagerung reiner Aliphaten; photokatalytisch von Furanen zu Pyrrolen; mit Ammoniak zu primären Arylaminen; Metallschrott recyceln mit ionischen Flüssigkeiten; terminale Alkene mit Ni‐Katalysatoren zum (Z)‐ oder (E)‐Alken isomerisieren;neue Fungizide, Medikamente und Alkaloide.</jats:p>","lang":"eng"}],"type":"journal_article","publication":"Nachrichten aus der Chemie","language":[{"iso":"eng"}],"user_id":"89271","department":[{"_id":"35"},{"_id":"2"}],"_id":"62087","citation":{"bibtex":"@article{Breugst_Andexer_Barra_Beil_Bierbach_Burkhardt_Dumele_Ernst_Frommer_Gellrich_et al._2025, title={Trendbericht: Organische Chemie 2025}, volume={73}, DOI={<a href=\"https://doi.org/10.1002/nadc.20254147860\">10.1002/nadc.20254147860</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Breugst, Martin and Andexer, Jennifer and Barra, Lena and Beil, Sebastian B. and Bierbach, Sascha and Burkhardt, Immo and Dumele, Oliver and Ernst, Martin and Frommer, Jennifer and Gellrich, Urs and et al.}, year={2025}, pages={40–70} }","short":"M. Breugst, J. Andexer, L. Barra, S.B. Beil, S. Bierbach, I. Burkhardt, O. Dumele, M. Ernst, J. Frommer, U. Gellrich, P. Germer, M. Giese, P. Huy, J. Klepp, K. Körber, M. Kordes, C.A. Kuttruff, T. Lindel, F. Pfrengle, B. Pieber, J. Pietruszka, N. Schaschke, M.O. Senge, N. Stadler, G. Storch, J.F. Teichert, S.R. Waldvogel, T. Werner, C. Winter, Nachrichten Aus Der Chemie 73 (2025) 40–70.","mla":"Breugst, Martin, et al. “Trendbericht: Organische Chemie 2025.” <i>Nachrichten Aus Der Chemie</i>, vol. 73, no. 3, Wiley, 2025, pp. 40–70, doi:<a href=\"https://doi.org/10.1002/nadc.20254147860\">10.1002/nadc.20254147860</a>.","apa":"Breugst, M., Andexer, J., Barra, L., Beil, S. B., Bierbach, S., Burkhardt, I., Dumele, O., Ernst, M., Frommer, J., Gellrich, U., Germer, P., Giese, M., Huy, P., Klepp, J., Körber, K., Kordes, M., Kuttruff, C. A., Lindel, T., Pfrengle, F., … Winter, C. (2025). Trendbericht: Organische Chemie 2025. <i>Nachrichten Aus Der Chemie</i>, <i>73</i>(3), 40–70. <a href=\"https://doi.org/10.1002/nadc.20254147860\">https://doi.org/10.1002/nadc.20254147860</a>","chicago":"Breugst, Martin, Jennifer Andexer, Lena Barra, Sebastian B. Beil, Sascha Bierbach, Immo Burkhardt, Oliver Dumele, et al. “Trendbericht: Organische Chemie 2025.” <i>Nachrichten Aus Der Chemie</i> 73, no. 3 (2025): 40–70. <a href=\"https://doi.org/10.1002/nadc.20254147860\">https://doi.org/10.1002/nadc.20254147860</a>.","ieee":"M. Breugst <i>et al.</i>, “Trendbericht: Organische Chemie 2025,” <i>Nachrichten aus der Chemie</i>, vol. 73, no. 3, pp. 40–70, 2025, doi: <a href=\"https://doi.org/10.1002/nadc.20254147860\">10.1002/nadc.20254147860</a>.","ama":"Breugst M, Andexer J, Barra L, et al. Trendbericht: Organische Chemie 2025. <i>Nachrichten aus der Chemie</i>. 2025;73(3):40-70. doi:<a href=\"https://doi.org/10.1002/nadc.20254147860\">10.1002/nadc.20254147860</a>"},"page":"40-70","intvolume":"        73","year":"2025","issue":"3","publication_status":"published","publication_identifier":{"issn":["1439-9598","1868-0054"]},"doi":"10.1002/nadc.20254147860","title":"Trendbericht: Organische Chemie 2025","date_created":"2025-11-05T15:11:51Z","author":[{"first_name":"Martin","full_name":"Breugst, Martin","last_name":"Breugst"},{"first_name":"Jennifer","last_name":"Andexer","full_name":"Andexer, Jennifer"},{"first_name":"Lena","last_name":"Barra","full_name":"Barra, Lena"},{"full_name":"Beil, Sebastian B.","last_name":"Beil","first_name":"Sebastian B."},{"last_name":"Bierbach","full_name":"Bierbach, Sascha","first_name":"Sascha"},{"last_name":"Burkhardt","full_name":"Burkhardt, Immo","first_name":"Immo"},{"last_name":"Dumele","full_name":"Dumele, Oliver","first_name":"Oliver"},{"first_name":"Martin","last_name":"Ernst","full_name":"Ernst, Martin"},{"first_name":"Jennifer","last_name":"Frommer","full_name":"Frommer, Jennifer"},{"full_name":"Gellrich, Urs","last_name":"Gellrich","first_name":"Urs"},{"full_name":"Germer, Philipp","last_name":"Germer","first_name":"Philipp"},{"first_name":"Michael","last_name":"Giese","full_name":"Giese, Michael"},{"last_name":"Huy","full_name":"Huy, Peter","first_name":"Peter"},{"full_name":"Klepp, Julian","last_name":"Klepp","first_name":"Julian"},{"first_name":"Karsten","full_name":"Körber, Karsten","last_name":"Körber"},{"last_name":"Kordes","full_name":"Kordes, Markus","first_name":"Markus"},{"last_name":"Kuttruff","full_name":"Kuttruff, Christian A.","first_name":"Christian A."},{"last_name":"Lindel","full_name":"Lindel, Thomas","first_name":"Thomas"},{"full_name":"Pfrengle, Fabian","last_name":"Pfrengle","first_name":"Fabian"},{"first_name":"Bartholomäus","full_name":"Pieber, Bartholomäus","last_name":"Pieber"},{"full_name":"Pietruszka, Jörg","last_name":"Pietruszka","first_name":"Jörg"},{"first_name":"Norbert","last_name":"Schaschke","full_name":"Schaschke, Norbert"},{"full_name":"Senge, Mathias O.","last_name":"Senge","first_name":"Mathias O."},{"last_name":"Stadler","full_name":"Stadler, Nina","first_name":"Nina"},{"first_name":"Golo","full_name":"Storch, Golo","last_name":"Storch"},{"last_name":"Teichert","full_name":"Teichert, Johannes F.","first_name":"Johannes F."},{"last_name":"Waldvogel","full_name":"Waldvogel, Siegfried R.","first_name":"Siegfried R."},{"last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"},{"first_name":"Christian","full_name":"Winter, Christian","last_name":"Winter"}],"volume":73,"date_updated":"2025-11-10T07:42:48Z","publisher":"Wiley"},{"citation":{"chicago":"Medvaric, Viktorija, Jan Paradies, and Thomas Werner. “Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides.” <i>Advanced Synthesis and Catalysis</i>, 2025. <a href=\"https://doi.org/10.1002/adsc.70059\">https://doi.org/10.1002/adsc.70059</a>.","ieee":"V. Medvaric, J. Paradies, and T. Werner, “Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides,” <i>Advanced Synthesis and Catalysis</i>, Art. no. 202500394, 2025, doi: <a href=\"https://doi.org/10.1002/adsc.70059\">10.1002/adsc.70059</a>.","ama":"Medvaric V, Paradies J, Werner T. Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides. <i>Advanced Synthesis and Catalysis</i>. Published online 2025. doi:<a href=\"https://doi.org/10.1002/adsc.70059\">10.1002/adsc.70059</a>","apa":"Medvaric, V., Paradies, J., &#38; Werner, T. (2025). Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides. <i>Advanced Synthesis and Catalysis</i>, Article 202500394. <a href=\"https://doi.org/10.1002/adsc.70059\">https://doi.org/10.1002/adsc.70059</a>","mla":"Medvaric, Viktorija, et al. “Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides.” <i>Advanced Synthesis and Catalysis</i>, 202500394, Wiley, 2025, doi:<a href=\"https://doi.org/10.1002/adsc.70059\">10.1002/adsc.70059</a>.","short":"V. Medvaric, J. Paradies, T. Werner, Advanced Synthesis and Catalysis (2025).","bibtex":"@article{Medvaric_Paradies_Werner_2025, title={Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides}, DOI={<a href=\"https://doi.org/10.1002/adsc.70059\">10.1002/adsc.70059</a>}, number={202500394}, journal={Advanced Synthesis and Catalysis}, publisher={Wiley}, author={Medvaric, Viktorija and Paradies, Jan and Werner, Thomas}, year={2025} }"},"year":"2025","publication_identifier":{"issn":["1615-4150","1615-4169"]},"publication_status":"published","doi":"10.1002/adsc.70059","title":"Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides","date_created":"2025-09-17T15:16:49Z","author":[{"first_name":"Viktorija","last_name":"Medvaric","id":"92677","full_name":"Medvaric, Viktorija"},{"full_name":"Paradies, Jan","id":"53339","orcid":"0000-0002-3698-668X","last_name":"Paradies","first_name":"Jan"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"date_updated":"2025-11-10T08:44:04Z","publisher":"Wiley","status":"public","abstract":[{"text":"<jats:p>Amidines are a ubiquitous class of bioactive compounds found in a wide variety of natural products; thus, efficient strategies for their preparation are in great demand. Herein, a novel protocol is reported for the synthesis of amidines based on P<jats:sup>III</jats:sup>/P<jats:sup>V</jats:sup>O redox catalysis. This two‐step, one‐pot approach involves the activation of amides via P<jats:sup>III</jats:sup>/P<jats:sup>V</jats:sup>O catalyzed in situ formation of imidoyl chloride intermediates which are directly converted upon reaction with amines into the corresponding amidines. Instead of traditionally used toxic and corrosive chloride sources, hexachloroacetone (HCA) is successfully employed as a halide source. The reaction proceeds with low catalyst loading (2 mol%) in BuOAc as the solvent. Under the optimized conditions, 20 amidines are prepared in yields up to 99%. A feasible mechanism is proposed based on experimental results. The synthetic potential of this method is evaluated in the preparation of the tyrosine kinase inhibitor (TKI) Erlotinib.</jats:p>","lang":"eng"}],"publication":"Advanced Synthesis and Catalysis","type":"journal_article","language":[{"iso":"eng"}],"keyword":["T2","T","CSSD"],"article_number":"202500394","department":[{"_id":"2"},{"_id":"389"}],"user_id":"89271","_id":"61335"},{"status":"public","type":"journal_article","_id":"62086","department":[{"_id":"35"},{"_id":"2"}],"user_id":"89271","intvolume":"        90","page":"12877-12887","citation":{"bibtex":"@article{Stefanow_Kell_Leduskrasta_Eh_Panten_Werner_2025, title={Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients}, volume={90}, DOI={<a href=\"https://doi.org/10.1021/acs.joc.5c00889\">10.1021/acs.joc.5c00889</a>}, number={37}, journal={The Journal of Organic Chemistry}, publisher={American Chemical Society (ACS)}, author={Stefanow, Vivian and Kell, Lukas and Leduskrasta, Aiga and Eh, Marcus and Panten, Johannes and Werner, Thomas}, year={2025}, pages={12877–12887} }","short":"V. Stefanow, L. Kell, A. Leduskrasta, M. Eh, J. Panten, T. Werner, The Journal of Organic Chemistry 90 (2025) 12877–12887.","mla":"Stefanow, Vivian, et al. “Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients.” <i>The Journal of Organic Chemistry</i>, vol. 90, no. 37, American Chemical Society (ACS), 2025, pp. 12877–87, doi:<a href=\"https://doi.org/10.1021/acs.joc.5c00889\">10.1021/acs.joc.5c00889</a>.","apa":"Stefanow, V., Kell, L., Leduskrasta, A., Eh, M., Panten, J., &#38; Werner, T. (2025). Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients. <i>The Journal of Organic Chemistry</i>, <i>90</i>(37), 12877–12887. <a href=\"https://doi.org/10.1021/acs.joc.5c00889\">https://doi.org/10.1021/acs.joc.5c00889</a>","ama":"Stefanow V, Kell L, Leduskrasta A, Eh M, Panten J, Werner T. Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients. <i>The Journal of Organic Chemistry</i>. 2025;90(37):12877-12887. doi:<a href=\"https://doi.org/10.1021/acs.joc.5c00889\">10.1021/acs.joc.5c00889</a>","ieee":"V. Stefanow, L. Kell, A. Leduskrasta, M. Eh, J. Panten, and T. Werner, “Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients,” <i>The Journal of Organic Chemistry</i>, vol. 90, no. 37, pp. 12877–12887, 2025, doi: <a href=\"https://doi.org/10.1021/acs.joc.5c00889\">10.1021/acs.joc.5c00889</a>.","chicago":"Stefanow, Vivian, Lukas Kell, Aiga Leduskrasta, Marcus Eh, Johannes Panten, and Thomas Werner. “Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients.” <i>The Journal of Organic Chemistry</i> 90, no. 37 (2025): 12877–87. <a href=\"https://doi.org/10.1021/acs.joc.5c00889\">https://doi.org/10.1021/acs.joc.5c00889</a>."},"publication_identifier":{"issn":["0022-3263","1520-6904"]},"publication_status":"published","doi":"10.1021/acs.joc.5c00889","date_updated":"2025-11-10T08:43:33Z","volume":90,"author":[{"first_name":"Vivian","full_name":"Stefanow, Vivian","last_name":"Stefanow"},{"last_name":"Kell","full_name":"Kell, Lukas","first_name":"Lukas"},{"first_name":"Aiga","full_name":"Leduskrasta, Aiga","last_name":"Leduskrasta"},{"first_name":"Marcus","full_name":"Eh, Marcus","last_name":"Eh"},{"full_name":"Panten, Johannes","last_name":"Panten","first_name":"Johannes"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"publication":"The Journal of Organic Chemistry","keyword":["T4","CSSD"],"language":[{"iso":"eng"}],"year":"2025","issue":"37","title":"Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients","publisher":"American Chemical Society (ACS)","date_created":"2025-11-05T15:10:13Z"},{"citation":{"chicago":"Zhou, Rundong, Viktorija Medvaric, Thomas Werner, and Jan Paradies. “Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance.” <i>Journal of the American Chemical Society</i>, 2025. <a href=\"https://doi.org/10.1021/jacs.5c06190\">https://doi.org/10.1021/jacs.5c06190</a>.","ieee":"R. Zhou, V. Medvaric, T. Werner, and J. Paradies, “Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance,” <i>Journal of the American Chemical Society</i>, Art. no. jacs. 5c06190, 2025, doi: <a href=\"https://doi.org/10.1021/jacs.5c06190\">10.1021/jacs.5c06190</a>.","ama":"Zhou R, Medvaric V, Werner T, Paradies J. Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance. <i>Journal of the American Chemical Society</i>. Published online 2025. doi:<a href=\"https://doi.org/10.1021/jacs.5c06190\">10.1021/jacs.5c06190</a>","apa":"Zhou, R., Medvaric, V., Werner, T., &#38; Paradies, J. (2025). Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance. <i>Journal of the American Chemical Society</i>, Article jacs. 5c06190. <a href=\"https://doi.org/10.1021/jacs.5c06190\">https://doi.org/10.1021/jacs.5c06190</a>","mla":"Zhou, Rundong, et al. “Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance.” <i>Journal of the American Chemical Society</i>, jacs. 5c06190, American Chemical Society (ACS), 2025, doi:<a href=\"https://doi.org/10.1021/jacs.5c06190\">10.1021/jacs.5c06190</a>.","bibtex":"@article{Zhou_Medvaric_Werner_Paradies_2025, title={Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance}, DOI={<a href=\"https://doi.org/10.1021/jacs.5c06190\">10.1021/jacs.5c06190</a>}, number={jacs. 5c06190}, journal={Journal of the American Chemical Society}, publisher={American Chemical Society (ACS)}, author={Zhou, Rundong and Medvaric, Viktorija and Werner, Thomas and Paradies, Jan}, year={2025} }","short":"R. Zhou, V. Medvaric, T. Werner, J. Paradies, Journal of the American Chemical Society (2025)."},"year":"2025","publication_status":"published","publication_identifier":{"issn":["0002-7863","1520-5126"]},"doi":"10.1021/jacs.5c06190","title":"Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance","author":[{"last_name":"Zhou","full_name":"Zhou, Rundong","first_name":"Rundong"},{"last_name":"Medvaric","id":"92677","full_name":"Medvaric, Viktorija","first_name":"Viktorija"},{"full_name":"Werner, Thomas","id":"89271","orcid":"https://orcid.org/0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"},{"last_name":"Paradies","orcid":"0000-0002-3698-668X","full_name":"Paradies, Jan","id":"53339","first_name":"Jan"}],"date_created":"2025-09-17T15:18:11Z","date_updated":"2025-11-10T08:43:50Z","publisher":"American Chemical Society (ACS)","status":"public","type":"journal_article","publication":"Journal of the American Chemical Society","language":[{"iso":"eng"}],"article_number":"jacs.5c06190","keyword":["T2","CSSD"],"user_id":"89271","department":[{"_id":"2"},{"_id":"389"}],"_id":"61336"},{"date_created":"2025-11-05T15:20:45Z","author":[{"last_name":"Breugst","full_name":"Breugst, Martin","first_name":"Martin"},{"first_name":"Jennifer","last_name":"Andexer","full_name":"Andexer, Jennifer"},{"first_name":"Lena","last_name":"Barra","full_name":"Barra, Lena"},{"first_name":"Sebastian B.","last_name":"Beil","full_name":"Beil, Sebastian B."},{"full_name":"Breinbauer, Rolf","last_name":"Breinbauer","first_name":"Rolf"},{"last_name":"Burkhardt","full_name":"Burkhardt, Immo","first_name":"Immo"},{"last_name":"Dumele","full_name":"Dumele, Oliver","first_name":"Oliver"},{"first_name":"Martin","last_name":"Ernst","full_name":"Ernst, Martin"},{"full_name":"Gellrich, Urs","last_name":"Gellrich","first_name":"Urs"},{"first_name":"Philipp","last_name":"Germer","full_name":"Germer, Philipp"},{"last_name":"Giese","full_name":"Giese, Michael","first_name":"Michael"},{"last_name":"Huy","full_name":"Huy, Peter","first_name":"Peter"},{"first_name":"Stephanie","last_name":"Kath‐Schorr","full_name":"Kath‐Schorr, Stephanie"},{"first_name":"Julian","full_name":"Klepp, Julian","last_name":"Klepp"},{"last_name":"Körber","full_name":"Körber, Karsten","first_name":"Karsten"},{"first_name":"Markus","last_name":"Kordes","full_name":"Kordes, Markus"},{"first_name":"Christian A.","last_name":"Kuttruff","full_name":"Kuttruff, Christian A."},{"last_name":"Lindel","full_name":"Lindel, Thomas","first_name":"Thomas"},{"first_name":"Sebastian","last_name":"Myllek","full_name":"Myllek, Sebastian"},{"first_name":"Fabian","full_name":"Pfrengle, Fabian","last_name":"Pfrengle"},{"first_name":"Jörg","last_name":"Pietruszka","full_name":"Pietruszka, Jörg"},{"first_name":"Norbert","last_name":"Schaschke","full_name":"Schaschke, Norbert"},{"full_name":"Senge, Mathias O.","last_name":"Senge","first_name":"Mathias O."},{"last_name":"Storch","full_name":"Storch, Golo","first_name":"Golo"},{"first_name":"Johannes F.","last_name":"Teichert","full_name":"Teichert, Johannes F."},{"full_name":"Tönjes, Jan","last_name":"Tönjes","first_name":"Jan"},{"first_name":"Siegfried R.","last_name":"Waldvogel","full_name":"Waldvogel, Siegfried R."},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner"},{"first_name":"Christian","last_name":"Winter","full_name":"Winter, Christian"}],"volume":72,"publisher":"Wiley","date_updated":"2025-11-10T07:46:36Z","doi":"10.1002/nadc.20244139258","title":"Trendbericht Organische Chemie 2024","issue":"3","publication_status":"published","publication_identifier":{"issn":["1439-9598","1868-0054"]},"citation":{"ama":"Breugst M, Andexer J, Barra L, et al. Trendbericht Organische Chemie 2024. <i>Nachrichten aus der Chemie</i>. 2024;72(3):44-67. doi:<a href=\"https://doi.org/10.1002/nadc.20244139258\">10.1002/nadc.20244139258</a>","ieee":"M. Breugst <i>et al.</i>, “Trendbericht Organische Chemie 2024,” <i>Nachrichten aus der Chemie</i>, vol. 72, no. 3, pp. 44–67, 2024, doi: <a href=\"https://doi.org/10.1002/nadc.20244139258\">10.1002/nadc.20244139258</a>.","chicago":"Breugst, Martin, Jennifer Andexer, Lena Barra, Sebastian B. Beil, Rolf Breinbauer, Immo Burkhardt, Oliver Dumele, et al. “Trendbericht Organische Chemie 2024.” <i>Nachrichten Aus Der Chemie</i> 72, no. 3 (2024): 44–67. <a href=\"https://doi.org/10.1002/nadc.20244139258\">https://doi.org/10.1002/nadc.20244139258</a>.","apa":"Breugst, M., Andexer, J., Barra, L., Beil, S. B., Breinbauer, R., Burkhardt, I., Dumele, O., Ernst, M., Gellrich, U., Germer, P., Giese, M., Huy, P., Kath‐Schorr, S., Klepp, J., Körber, K., Kordes, M., Kuttruff, C. A., Lindel, T., Myllek, S., … Winter, C. (2024). Trendbericht Organische Chemie 2024. <i>Nachrichten Aus Der Chemie</i>, <i>72</i>(3), 44–67. <a href=\"https://doi.org/10.1002/nadc.20244139258\">https://doi.org/10.1002/nadc.20244139258</a>","mla":"Breugst, Martin, et al. “Trendbericht Organische Chemie 2024.” <i>Nachrichten Aus Der Chemie</i>, vol. 72, no. 3, Wiley, 2024, pp. 44–67, doi:<a href=\"https://doi.org/10.1002/nadc.20244139258\">10.1002/nadc.20244139258</a>.","short":"M. Breugst, J. Andexer, L. Barra, S.B. Beil, R. Breinbauer, I. Burkhardt, O. Dumele, M. Ernst, U. Gellrich, P. Germer, M. Giese, P. Huy, S. Kath‐Schorr, J. Klepp, K. Körber, M. Kordes, C.A. Kuttruff, T. Lindel, S. Myllek, F. Pfrengle, J. Pietruszka, N. Schaschke, M.O. Senge, G. Storch, J.F. Teichert, J. Tönjes, S.R. Waldvogel, T. Werner, C. Winter, Nachrichten Aus Der Chemie 72 (2024) 44–67.","bibtex":"@article{Breugst_Andexer_Barra_Beil_Breinbauer_Burkhardt_Dumele_Ernst_Gellrich_Germer_et al._2024, title={Trendbericht Organische Chemie 2024}, volume={72}, DOI={<a href=\"https://doi.org/10.1002/nadc.20244139258\">10.1002/nadc.20244139258</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Breugst, Martin and Andexer, Jennifer and Barra, Lena and Beil, Sebastian B. and Breinbauer, Rolf and Burkhardt, Immo and Dumele, Oliver and Ernst, Martin and Gellrich, Urs and Germer, Philipp and et al.}, year={2024}, pages={44–67} }"},"page":"44-67","intvolume":"        72","year":"2024","user_id":"89271","department":[{"_id":"35"},{"_id":"2"}],"_id":"62093","language":[{"iso":"eng"}],"type":"journal_article","publication":"Nachrichten aus der Chemie","status":"public","abstract":[{"lang":"eng","text":"<jats:title>Abstract</jats:title><jats:p>Unter anderem das hat die Organik im letzten Jahr bewegt: milde Oxidation mit Elektrochemie, Oxidation zu enantiomerenreinen Sulfonylverbindungen, Flüssigkristallphasen erkennen mit maschinellem Lernen, CO<jats:sub>2</jats:sub>reagiert zu Succinat und Carbamaten, eine Alternative zu Bisphenol A, Subporphyrine, photoschaltbare Spinmaterialien, photochemische Thiophen‐Ringerweiterung, und Peptide werden mit Bor versehen und cyclisiert. Die Zusammenstellung des Trendberichts koordiniert hat Martin Breugst, Universität Chemnitz.</jats:p>"}]},{"keyword":["T4"],"language":[{"iso":"eng"}],"_id":"62092","user_id":"89271","department":[{"_id":"35"},{"_id":"2"}],"status":"public","type":"journal_article","publication":"Phytochemistry Letters","title":"Design, isolation, synthesis, and mechanistic insight of flavonoids isolated from Beilschmiedia obscura, as potential α-glucosidase inhibitors","doi":"10.1016/j.phytol.2024.06.004","date_updated":"2025-11-10T07:45:58Z","publisher":"Elsevier BV","date_created":"2025-11-05T15:18:32Z","author":[{"first_name":"Suzanne L.","last_name":"Nyemeck","full_name":"Nyemeck, Suzanne L."},{"last_name":"Eyong","full_name":"Eyong, Kenneth O.","first_name":"Kenneth O."},{"first_name":"Ronald","last_name":"Bidingha","full_name":"Bidingha, Ronald"},{"first_name":"Michael HK.","full_name":"Kamdem, Michael HK.","last_name":"Kamdem"},{"full_name":"Ndinteh, Derek T.","last_name":"Ndinteh","first_name":"Derek T."},{"last_name":"Odumosu","full_name":"Odumosu, Patricia O.","first_name":"Patricia O."},{"first_name":"Gabriel N.","last_name":"Folefoc","full_name":"Folefoc, Gabriel N."},{"first_name":"Danielle C.","last_name":"Bilanda","full_name":"Bilanda, Danielle C."},{"full_name":"Egbe, Andrew E.","last_name":"Egbe","first_name":"Andrew E."},{"full_name":"Werner, Thomas","id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"},{"first_name":"Boris D.","last_name":"Bekono","full_name":"Bekono, Boris D."},{"first_name":"Fidele","last_name":"Ntie-Kang","full_name":"Ntie-Kang, Fidele"}],"volume":62,"year":"2024","citation":{"ieee":"S. L. Nyemeck <i>et al.</i>, “Design, isolation, synthesis, and mechanistic insight of flavonoids isolated from Beilschmiedia obscura, as potential α-glucosidase inhibitors,” <i>Phytochemistry Letters</i>, vol. 62, pp. 59–67, 2024, doi: <a href=\"https://doi.org/10.1016/j.phytol.2024.06.004\">10.1016/j.phytol.2024.06.004</a>.","chicago":"Nyemeck, Suzanne L., Kenneth O. Eyong, Ronald Bidingha, Michael HK. Kamdem, Derek T. Ndinteh, Patricia O. Odumosu, Gabriel N. Folefoc, et al. “Design, Isolation, Synthesis, and Mechanistic Insight of Flavonoids Isolated from Beilschmiedia Obscura, as Potential α-Glucosidase Inhibitors.” <i>Phytochemistry Letters</i> 62 (2024): 59–67. <a href=\"https://doi.org/10.1016/j.phytol.2024.06.004\">https://doi.org/10.1016/j.phytol.2024.06.004</a>.","ama":"Nyemeck SL, Eyong KO, Bidingha R, et al. Design, isolation, synthesis, and mechanistic insight of flavonoids isolated from Beilschmiedia obscura, as potential α-glucosidase inhibitors. <i>Phytochemistry Letters</i>. 2024;62:59-67. doi:<a href=\"https://doi.org/10.1016/j.phytol.2024.06.004\">10.1016/j.phytol.2024.06.004</a>","bibtex":"@article{Nyemeck_Eyong_Bidingha_Kamdem_Ndinteh_Odumosu_Folefoc_Bilanda_Egbe_Werner_et al._2024, title={Design, isolation, synthesis, and mechanistic insight of flavonoids isolated from Beilschmiedia obscura, as potential α-glucosidase inhibitors}, volume={62}, DOI={<a href=\"https://doi.org/10.1016/j.phytol.2024.06.004\">10.1016/j.phytol.2024.06.004</a>}, journal={Phytochemistry Letters}, publisher={Elsevier BV}, author={Nyemeck, Suzanne L. and Eyong, Kenneth O. and Bidingha, Ronald and Kamdem, Michael HK. and Ndinteh, Derek T. and Odumosu, Patricia O. and Folefoc, Gabriel N. and Bilanda, Danielle C. and Egbe, Andrew E. and Werner, Thomas and et al.}, year={2024}, pages={59–67} }","short":"S.L. Nyemeck, K.O. Eyong, R. Bidingha, M.HK. Kamdem, D.T. Ndinteh, P.O. Odumosu, G.N. Folefoc, D.C. Bilanda, A.E. Egbe, T. Werner, B.D. Bekono, F. Ntie-Kang, Phytochemistry Letters 62 (2024) 59–67.","mla":"Nyemeck, Suzanne L., et al. “Design, Isolation, Synthesis, and Mechanistic Insight of Flavonoids Isolated from Beilschmiedia Obscura, as Potential α-Glucosidase Inhibitors.” <i>Phytochemistry Letters</i>, vol. 62, Elsevier BV, 2024, pp. 59–67, doi:<a href=\"https://doi.org/10.1016/j.phytol.2024.06.004\">10.1016/j.phytol.2024.06.004</a>.","apa":"Nyemeck, S. L., Eyong, K. O., Bidingha, R., Kamdem, M. HK., Ndinteh, D. T., Odumosu, P. O., Folefoc, G. N., Bilanda, D. C., Egbe, A. E., Werner, T., Bekono, B. D., &#38; Ntie-Kang, F. (2024). Design, isolation, synthesis, and mechanistic insight of flavonoids isolated from Beilschmiedia obscura, as potential α-glucosidase inhibitors. <i>Phytochemistry Letters</i>, <i>62</i>, 59–67. <a href=\"https://doi.org/10.1016/j.phytol.2024.06.004\">https://doi.org/10.1016/j.phytol.2024.06.004</a>"},"intvolume":"        62","page":"59-67","publication_status":"published","publication_identifier":{"issn":["1874-3900"]}},{"citation":{"apa":"Ren, C., Terazzi, C., &#38; Werner, T. (2024). Tuneable reduction of CO<sub>2</sub> – organocatalyzed selective formylation and methylation of amines. <i>Green Chemistry</i>, <i>26</i>(1), 439–447. <a href=\"https://doi.org/10.1039/d3gc03993e\">https://doi.org/10.1039/d3gc03993e</a>","short":"C. Ren, C. Terazzi, T. Werner, Green Chemistry 26 (2024) 439–447.","bibtex":"@article{Ren_Terazzi_Werner_2024, title={Tuneable reduction of CO<sub>2</sub> – organocatalyzed selective formylation and methylation of amines}, volume={26}, DOI={<a href=\"https://doi.org/10.1039/d3gc03993e\">10.1039/d3gc03993e</a>}, number={1}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Ren, Changyue and Terazzi, Constanza and Werner, Thomas}, year={2024}, pages={439–447} }","mla":"Ren, Changyue, et al. “Tuneable Reduction of CO<sub>2</sub> – Organocatalyzed Selective Formylation and Methylation of Amines.” <i>Green Chemistry</i>, vol. 26, no. 1, Royal Society of Chemistry (RSC), 2024, pp. 439–47, doi:<a href=\"https://doi.org/10.1039/d3gc03993e\">10.1039/d3gc03993e</a>.","chicago":"Ren, Changyue, Constanza Terazzi, and Thomas Werner. “Tuneable Reduction of CO<sub>2</sub> – Organocatalyzed Selective Formylation and Methylation of Amines.” <i>Green Chemistry</i> 26, no. 1 (2024): 439–47. <a href=\"https://doi.org/10.1039/d3gc03993e\">https://doi.org/10.1039/d3gc03993e</a>.","ieee":"C. Ren, C. Terazzi, and T. Werner, “Tuneable reduction of CO<sub>2</sub> – organocatalyzed selective formylation and methylation of amines,” <i>Green Chemistry</i>, vol. 26, no. 1, pp. 439–447, 2024, doi: <a href=\"https://doi.org/10.1039/d3gc03993e\">10.1039/d3gc03993e</a>.","ama":"Ren C, Terazzi C, Werner T. Tuneable reduction of CO<sub>2</sub> – organocatalyzed selective formylation and methylation of amines. <i>Green Chemistry</i>. 2024;26(1):439-447. doi:<a href=\"https://doi.org/10.1039/d3gc03993e\">10.1039/d3gc03993e</a>"},"page":"439-447","intvolume":"        26","year":"2024","issue":"1","publication_status":"published","publication_identifier":{"issn":["1463-9262","1463-9270"]},"doi":"10.1039/d3gc03993e","title":"Tuneable reduction of CO<sub>2</sub> – organocatalyzed selective formylation and methylation of amines","date_created":"2025-11-05T15:16:32Z","author":[{"first_name":"Changyue","full_name":"Ren, Changyue","last_name":"Ren"},{"first_name":"Constanza","full_name":"Terazzi, Constanza","last_name":"Terazzi"},{"orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271","first_name":"Thomas"}],"volume":26,"date_updated":"2025-11-10T08:44:44Z","publisher":"Royal Society of Chemistry (RSC)","status":"public","abstract":[{"text":"<jats:p>The selective <jats:italic>N</jats:italic>-formylation and <jats:italic>N</jats:italic>-methylation of amines with carbon dioxide (CO<jats:sub>2</jats:sub>) catalyzed by methyltriphenylphosphonium methylcarbonate and tuned by polymethylhydrosiloxane or trimethoxysilane as reducing agents is reported.</jats:p>","lang":"eng"}],"type":"journal_article","publication":"Green Chemistry","language":[{"iso":"eng"}],"keyword":["T1","T2","CSSD"],"user_id":"89271","department":[{"_id":"35"},{"_id":"2"}],"_id":"62090"},{"year":"2024","page":"10969-10977","intvolume":"        12","citation":{"ieee":"C. Ren, A. Spannenberg, and T. Werner, “Phosphonium-Salt-Catalyzed <i>N</i>-Methylation and <i>N</i>-Formylation of Amines with CO<sub>2</sub>,” <i>ACS Sustainable Chemistry &#38;amp; Engineering</i>, vol. 12, no. 29, pp. 10969–10977, 2024, doi: <a href=\"https://doi.org/10.1021/acssuschemeng.4c03464\">10.1021/acssuschemeng.4c03464</a>.","chicago":"Ren, Changyue, Anke Spannenberg, and Thomas Werner. “Phosphonium-Salt-Catalyzed <i>N</i>-Methylation and <i>N</i>-Formylation of Amines with CO<sub>2</sub>.” <i>ACS Sustainable Chemistry &#38;amp; Engineering</i> 12, no. 29 (2024): 10969–77. <a href=\"https://doi.org/10.1021/acssuschemeng.4c03464\">https://doi.org/10.1021/acssuschemeng.4c03464</a>.","ama":"Ren C, Spannenberg A, Werner T. Phosphonium-Salt-Catalyzed <i>N</i>-Methylation and <i>N</i>-Formylation of Amines with CO<sub>2</sub>. <i>ACS Sustainable Chemistry &#38;amp; Engineering</i>. 2024;12(29):10969-10977. doi:<a href=\"https://doi.org/10.1021/acssuschemeng.4c03464\">10.1021/acssuschemeng.4c03464</a>","short":"C. Ren, A. Spannenberg, T. Werner, ACS Sustainable Chemistry &#38;amp; Engineering 12 (2024) 10969–10977.","mla":"Ren, Changyue, et al. “Phosphonium-Salt-Catalyzed <i>N</i>-Methylation and <i>N</i>-Formylation of Amines with CO<sub>2</sub>.” <i>ACS Sustainable Chemistry &#38;amp; Engineering</i>, vol. 12, no. 29, American Chemical Society (ACS), 2024, pp. 10969–77, doi:<a href=\"https://doi.org/10.1021/acssuschemeng.4c03464\">10.1021/acssuschemeng.4c03464</a>.","bibtex":"@article{Ren_Spannenberg_Werner_2024, title={Phosphonium-Salt-Catalyzed <i>N</i>-Methylation and <i>N</i>-Formylation of Amines with CO<sub>2</sub>}, volume={12}, DOI={<a href=\"https://doi.org/10.1021/acssuschemeng.4c03464\">10.1021/acssuschemeng.4c03464</a>}, number={29}, journal={ACS Sustainable Chemistry &#38;amp; Engineering}, publisher={American Chemical Society (ACS)}, author={Ren, Changyue and Spannenberg, Anke and Werner, Thomas}, year={2024}, pages={10969–10977} }","apa":"Ren, C., Spannenberg, A., &#38; Werner, T. (2024). Phosphonium-Salt-Catalyzed <i>N</i>-Methylation and <i>N</i>-Formylation of Amines with CO<sub>2</sub>. <i>ACS Sustainable Chemistry &#38;amp; Engineering</i>, <i>12</i>(29), 10969–10977. <a href=\"https://doi.org/10.1021/acssuschemeng.4c03464\">https://doi.org/10.1021/acssuschemeng.4c03464</a>"},"publication_identifier":{"issn":["2168-0485","2168-0485"]},"publication_status":"published","issue":"29","title":"Phosphonium-Salt-Catalyzed <i>N</i>-Methylation and <i>N</i>-Formylation of Amines with CO<sub>2</sub>","doi":"10.1021/acssuschemeng.4c03464","date_updated":"2025-11-10T08:45:58Z","publisher":"American Chemical Society (ACS)","volume":12,"date_created":"2025-11-05T15:17:55Z","author":[{"first_name":"Changyue","last_name":"Ren","full_name":"Ren, Changyue"},{"full_name":"Spannenberg, Anke","last_name":"Spannenberg","first_name":"Anke"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"status":"public","publication":"ACS Sustainable Chemistry &amp; Engineering","type":"journal_article","keyword":["T1","T2","CSSD"],"language":[{"iso":"eng"}],"_id":"62091","department":[{"_id":"35"},{"_id":"2"}],"user_id":"89271"},{"publication":"Nachrichten aus der Chemie","abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>Polystyrolproben werden mit Eisen(III)chlorid und weißen LEDs zu Oligomeren und Benzoylprodukten; ein Wolframatkatalysator invertiert die Absolutkonfiguration an sp<jats:sup>3</jats:sup>‐Kohlenstoffzentren; gelöstes Rätsel um eine symmetrieverbotene konrotatorische 14‐Elektronen‐Elektrocyclisierung; Polycarbonate, die sich ohne Lösungsmittel recyceln lassen: Highlights von Oktober 2021 bis 2022.</jats:p>","lang":"eng"}],"language":[{"iso":"eng"}],"issue":"3","year":"2023","date_created":"2025-11-05T15:23:42Z","publisher":"Wiley","title":"Trendbericht Organische Chemie 2023","type":"journal_article","status":"public","department":[{"_id":"35"},{"_id":"2"}],"user_id":"89271","_id":"62097","publication_identifier":{"issn":["1439-9598","1868-0054"]},"publication_status":"published","intvolume":"        71","page":"40-66","citation":{"apa":"Breugst, M., Andexer, J. N., Beil, S. B., Breinbauer, R., Dumele, O., Ernst, M., Gellrich, U., Germer, P., Giese, M., Gulder, T. A. M., Huy, P., Hüttel, W., Kath‐Schorr, S., Körber, K., Kordes, M., Kuttruff, C., Lindel, T., Meier, R., Myllek, S., … Winter, C. (2023). Trendbericht Organische Chemie 2023. <i>Nachrichten Aus Der Chemie</i>, <i>71</i>(3), 40–66. <a href=\"https://doi.org/10.1002/nadc.20234135542\">https://doi.org/10.1002/nadc.20234135542</a>","short":"M. Breugst, J.N. Andexer, S.B. Beil, R. Breinbauer, O. Dumele, M. Ernst, U. Gellrich, P. Germer, M. Giese, T.A.M. Gulder, P. Huy, W. Hüttel, S. Kath‐Schorr, K. Körber, M. Kordes, C. Kuttruff, T. Lindel, R. Meier, S. Myllek, N. Schaschke, F. Pfrengle, J. Pietruszka, H. Sebode, M.O. Senge, G. Storch, B.F. Straub, J. Teichert, S.R. Waldvogel, T. Werner, C. Winter, Nachrichten Aus Der Chemie 71 (2023) 40–66.","mla":"Breugst, Martin, et al. “Trendbericht Organische Chemie 2023.” <i>Nachrichten Aus Der Chemie</i>, vol. 71, no. 3, Wiley, 2023, pp. 40–66, doi:<a href=\"https://doi.org/10.1002/nadc.20234135542\">10.1002/nadc.20234135542</a>.","bibtex":"@article{Breugst_Andexer_Beil_Breinbauer_Dumele_Ernst_Gellrich_Germer_Giese_Gulder_et al._2023, title={Trendbericht Organische Chemie 2023}, volume={71}, DOI={<a href=\"https://doi.org/10.1002/nadc.20234135542\">10.1002/nadc.20234135542</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Breugst, Martin and Andexer, Jennifer N. and Beil, Sebastian B. and Breinbauer, Rolf and Dumele, Oliver and Ernst, Martin and Gellrich, Urs and Germer, Philipp and Giese, Michael and Gulder, Tobias A. M. and et al.}, year={2023}, pages={40–66} }","ama":"Breugst M, Andexer JN, Beil SB, et al. Trendbericht Organische Chemie 2023. <i>Nachrichten aus der Chemie</i>. 2023;71(3):40-66. doi:<a href=\"https://doi.org/10.1002/nadc.20234135542\">10.1002/nadc.20234135542</a>","chicago":"Breugst, Martin, Jennifer N. Andexer, Sebastian B. Beil, Rolf Breinbauer, Oliver Dumele, Martin Ernst, Urs Gellrich, et al. “Trendbericht Organische Chemie 2023.” <i>Nachrichten Aus Der Chemie</i> 71, no. 3 (2023): 40–66. <a href=\"https://doi.org/10.1002/nadc.20234135542\">https://doi.org/10.1002/nadc.20234135542</a>.","ieee":"M. Breugst <i>et al.</i>, “Trendbericht Organische Chemie 2023,” <i>Nachrichten aus der Chemie</i>, vol. 71, no. 3, pp. 40–66, 2023, doi: <a href=\"https://doi.org/10.1002/nadc.20234135542\">10.1002/nadc.20234135542</a>."},"volume":71,"author":[{"first_name":"Martin","full_name":"Breugst, Martin","last_name":"Breugst"},{"full_name":"Andexer, Jennifer N.","last_name":"Andexer","first_name":"Jennifer N."},{"first_name":"Sebastian B.","last_name":"Beil","full_name":"Beil, Sebastian B."},{"first_name":"Rolf","last_name":"Breinbauer","full_name":"Breinbauer, Rolf"},{"last_name":"Dumele","full_name":"Dumele, Oliver","first_name":"Oliver"},{"first_name":"Martin","full_name":"Ernst, Martin","last_name":"Ernst"},{"first_name":"Urs","full_name":"Gellrich, Urs","last_name":"Gellrich"},{"first_name":"Philipp","full_name":"Germer, Philipp","last_name":"Germer"},{"first_name":"Michael","full_name":"Giese, Michael","last_name":"Giese"},{"full_name":"Gulder, Tobias A. M.","last_name":"Gulder","first_name":"Tobias A. M."},{"first_name":"Peter","last_name":"Huy","full_name":"Huy, Peter"},{"full_name":"Hüttel, Wolfgang","last_name":"Hüttel","first_name":"Wolfgang"},{"full_name":"Kath‐Schorr, Stephanie","last_name":"Kath‐Schorr","first_name":"Stephanie"},{"full_name":"Körber, Karsten","last_name":"Körber","first_name":"Karsten"},{"last_name":"Kordes","full_name":"Kordes, Markus","first_name":"Markus"},{"first_name":"Christian","last_name":"Kuttruff","full_name":"Kuttruff, Christian"},{"first_name":"Thomas","full_name":"Lindel, Thomas","last_name":"Lindel"},{"last_name":"Meier","full_name":"Meier, Robin","first_name":"Robin"},{"last_name":"Myllek","full_name":"Myllek, Sebastian","first_name":"Sebastian"},{"last_name":"Schaschke","full_name":"Schaschke, Norbert","first_name":"Norbert"},{"first_name":"Fabian","full_name":"Pfrengle, Fabian","last_name":"Pfrengle"},{"first_name":"Jörg","full_name":"Pietruszka, Jörg","last_name":"Pietruszka"},{"last_name":"Sebode","full_name":"Sebode, Hanna","first_name":"Hanna"},{"last_name":"Senge","full_name":"Senge, Mathias O.","first_name":"Mathias O."},{"first_name":"Golo","full_name":"Storch, Golo","last_name":"Storch"},{"first_name":"Bernd F.","full_name":"Straub, Bernd F.","last_name":"Straub"},{"first_name":"Johannes","full_name":"Teichert, Johannes","last_name":"Teichert"},{"last_name":"Waldvogel","full_name":"Waldvogel, Siegfried R.","first_name":"Siegfried R."},{"orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271","first_name":"Thomas"},{"first_name":"Christian","last_name":"Winter","full_name":"Winter, Christian"}],"date_updated":"2025-11-10T07:49:42Z","doi":"10.1002/nadc.20234135542"},{"publication_identifier":{"issn":["1874-3900"]},"publication_status":"published","intvolume":"        57","page":"26-35","citation":{"mla":"Yemback, Pierre, et al. “Lupane Derivatives: Design, Isolation, Synthesis and Evaluation of Antiplasmodial Activity against Plasmodium Falciparum 3D7 Strain.” <i>Phytochemistry Letters</i>, vol. 57, Elsevier BV, 2023, pp. 26–35, doi:<a href=\"https://doi.org/10.1016/j.phytol.2023.06.009\">10.1016/j.phytol.2023.06.009</a>.","short":"P. Yemback, K.O. Eyong, N.M. Efange, M.HK. Kamdem, D.T. Ndinteh, P.O. Odumosu, G.N. Folefoc, L. Ayong, T. Werner, Phytochemistry Letters 57 (2023) 26–35.","bibtex":"@article{Yemback_Eyong_Efange_Kamdem_Ndinteh_Odumosu_Folefoc_Ayong_Werner_2023, title={Lupane derivatives: Design, isolation, synthesis and evaluation of antiplasmodial activity against Plasmodium falciparum 3D7 strain}, volume={57}, DOI={<a href=\"https://doi.org/10.1016/j.phytol.2023.06.009\">10.1016/j.phytol.2023.06.009</a>}, journal={Phytochemistry Letters}, publisher={Elsevier BV}, author={Yemback, Pierre and Eyong, Kenneth O. and Efange, Noella M. and Kamdem, Michael HK. and Ndinteh, Derek T. and Odumosu, Patricia O. and Folefoc, Gabriel N. and Ayong, Lawrence and Werner, Thomas}, year={2023}, pages={26–35} }","apa":"Yemback, P., Eyong, K. O., Efange, N. M., Kamdem, M. HK., Ndinteh, D. T., Odumosu, P. O., Folefoc, G. N., Ayong, L., &#38; Werner, T. (2023). Lupane derivatives: Design, isolation, synthesis and evaluation of antiplasmodial activity against Plasmodium falciparum 3D7 strain. <i>Phytochemistry Letters</i>, <i>57</i>, 26–35. <a href=\"https://doi.org/10.1016/j.phytol.2023.06.009\">https://doi.org/10.1016/j.phytol.2023.06.009</a>","chicago":"Yemback, Pierre, Kenneth O. Eyong, Noella M. Efange, Michael HK. Kamdem, Derek T. Ndinteh, Patricia O. Odumosu, Gabriel N. Folefoc, Lawrence Ayong, and Thomas Werner. “Lupane Derivatives: Design, Isolation, Synthesis and Evaluation of Antiplasmodial Activity against Plasmodium Falciparum 3D7 Strain.” <i>Phytochemistry Letters</i> 57 (2023): 26–35. <a href=\"https://doi.org/10.1016/j.phytol.2023.06.009\">https://doi.org/10.1016/j.phytol.2023.06.009</a>.","ieee":"P. Yemback <i>et al.</i>, “Lupane derivatives: Design, isolation, synthesis and evaluation of antiplasmodial activity against Plasmodium falciparum 3D7 strain,” <i>Phytochemistry Letters</i>, vol. 57, pp. 26–35, 2023, doi: <a href=\"https://doi.org/10.1016/j.phytol.2023.06.009\">10.1016/j.phytol.2023.06.009</a>.","ama":"Yemback P, Eyong KO, Efange NM, et al. Lupane derivatives: Design, isolation, synthesis and evaluation of antiplasmodial activity against Plasmodium falciparum 3D7 strain. <i>Phytochemistry Letters</i>. 2023;57:26-35. doi:<a href=\"https://doi.org/10.1016/j.phytol.2023.06.009\">10.1016/j.phytol.2023.06.009</a>"},"year":"2023","volume":57,"date_created":"2025-11-05T15:21:35Z","author":[{"full_name":"Yemback, Pierre","last_name":"Yemback","first_name":"Pierre"},{"first_name":"Kenneth O.","full_name":"Eyong, Kenneth O.","last_name":"Eyong"},{"full_name":"Efange, Noella M.","last_name":"Efange","first_name":"Noella M."},{"first_name":"Michael HK.","full_name":"Kamdem, Michael HK.","last_name":"Kamdem"},{"first_name":"Derek T.","last_name":"Ndinteh","full_name":"Ndinteh, Derek T."},{"last_name":"Odumosu","full_name":"Odumosu, Patricia O.","first_name":"Patricia O."},{"full_name":"Folefoc, Gabriel N.","last_name":"Folefoc","first_name":"Gabriel N."},{"full_name":"Ayong, Lawrence","last_name":"Ayong","first_name":"Lawrence"},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner"}],"date_updated":"2025-11-10T07:47:25Z","publisher":"Elsevier BV","doi":"10.1016/j.phytol.2023.06.009","title":"Lupane derivatives: Design, isolation, synthesis and evaluation of antiplasmodial activity against Plasmodium falciparum 3D7 strain","publication":"Phytochemistry Letters","type":"journal_article","status":"public","department":[{"_id":"35"},{"_id":"2"}],"user_id":"89271","_id":"62094","language":[{"iso":"eng"}],"keyword":["T4"]},{"user_id":"89271","department":[{"_id":"35"},{"_id":"2"}],"_id":"62096","language":[{"iso":"eng"}],"article_number":"e202300917","keyword":["T1","T4","CSSD"],"type":"journal_article","publication":"ChemCatChem","status":"public","abstract":[{"lang":"eng","text":"<jats:title>Abstract</jats:title><jats:p>The biocatalytic kinetic resolution of cyclic carbonates derived from glycerol is reported. A selection of 26 esterases and lipases was tested for the asymmetric hydrolysis of the model substrate (epichlorohydrin carbonate) in aqueous medium. Among them, Pig Liver Esterase and Novozym® 435 showed the best selectivity with <jats:italic>E</jats:italic>=38 and 49, respectively. Both enzymes were employed for the conversion of 12 glycerol derivatives under optimized conditions. The resolution of halogenated carbonates afforded the unconverted enantiomer in up to &gt;99 : 1 <jats:italic>er</jats:italic>. Furthermore, Novozym® 435 was successfully recycled 10 times without significant loss of activity. Upscaling and isolation of the chiral carbonate was also demonstrated. Subsequent conversion of this chiral building block allowed the direct one‐pot synthesis of (<jats:italic>S</jats:italic>)‐Guaifenesin, (<jats:italic>S</jats:italic>)‐Mephenesin and (<jats:italic>S</jats:italic>)‐Chlorphenesin in up to 89 % yield and 94 : 6 <jats:italic>er</jats:italic>.</jats:p>"}],"author":[{"first_name":"Constanza","last_name":"Terazzi","full_name":"Terazzi, Constanza"},{"last_name":"Spannenberg","full_name":"Spannenberg, Anke","first_name":"Anke"},{"last_name":"von Langermann","full_name":"von Langermann, Jan","first_name":"Jan"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271","full_name":"Werner, Thomas"}],"date_created":"2025-11-05T15:23:21Z","volume":15,"publisher":"Wiley","date_updated":"2025-11-10T08:46:22Z","doi":"10.1002/cctc.202300917","title":"Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates","issue":"19","publication_status":"published","publication_identifier":{"issn":["1867-3880","1867-3899"]},"citation":{"ama":"Terazzi C, Spannenberg A, von Langermann J, Werner T. Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates. <i>ChemCatChem</i>. 2023;15(19). doi:<a href=\"https://doi.org/10.1002/cctc.202300917\">10.1002/cctc.202300917</a>","ieee":"C. Terazzi, A. Spannenberg, J. von Langermann, and T. Werner, “Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates,” <i>ChemCatChem</i>, vol. 15, no. 19, Art. no. e202300917, 2023, doi: <a href=\"https://doi.org/10.1002/cctc.202300917\">10.1002/cctc.202300917</a>.","chicago":"Terazzi, Constanza, Anke Spannenberg, Jan von Langermann, and Thomas Werner. “Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates.” <i>ChemCatChem</i> 15, no. 19 (2023). <a href=\"https://doi.org/10.1002/cctc.202300917\">https://doi.org/10.1002/cctc.202300917</a>.","apa":"Terazzi, C., Spannenberg, A., von Langermann, J., &#38; Werner, T. (2023). Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates. <i>ChemCatChem</i>, <i>15</i>(19), Article e202300917. <a href=\"https://doi.org/10.1002/cctc.202300917\">https://doi.org/10.1002/cctc.202300917</a>","mla":"Terazzi, Constanza, et al. “Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates.” <i>ChemCatChem</i>, vol. 15, no. 19, e202300917, Wiley, 2023, doi:<a href=\"https://doi.org/10.1002/cctc.202300917\">10.1002/cctc.202300917</a>.","short":"C. Terazzi, A. Spannenberg, J. von Langermann, T. Werner, ChemCatChem 15 (2023).","bibtex":"@article{Terazzi_Spannenberg_von Langermann_Werner_2023, title={Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates}, volume={15}, DOI={<a href=\"https://doi.org/10.1002/cctc.202300917\">10.1002/cctc.202300917</a>}, number={19e202300917}, journal={ChemCatChem}, publisher={Wiley}, author={Terazzi, Constanza and Spannenberg, Anke and von Langermann, Jan and Werner, Thomas}, year={2023} }"},"intvolume":"        15","year":"2023"},{"status":"public","publication":"Organic Letters","type":"journal_article","keyword":["T2","CSSD"],"language":[{"iso":"eng"}],"_id":"62095","department":[{"_id":"35"},{"_id":"2"}],"user_id":"89271","year":"2023","page":"9114-9118","intvolume":"        25","citation":{"bibtex":"@article{Tönjes_Kell_Werner_2023, title={Organocatalytic Stereospecific Appel Reaction}, volume={25}, DOI={<a href=\"https://doi.org/10.1021/acs.orglett.3c03463\">10.1021/acs.orglett.3c03463</a>}, number={51}, journal={Organic Letters}, publisher={American Chemical Society (ACS)}, author={Tönjes, Jan and Kell, Lukas and Werner, Thomas}, year={2023}, pages={9114–9118} }","mla":"Tönjes, Jan, et al. “Organocatalytic Stereospecific Appel Reaction.” <i>Organic Letters</i>, vol. 25, no. 51, American Chemical Society (ACS), 2023, pp. 9114–18, doi:<a href=\"https://doi.org/10.1021/acs.orglett.3c03463\">10.1021/acs.orglett.3c03463</a>.","short":"J. Tönjes, L. Kell, T. Werner, Organic Letters 25 (2023) 9114–9118.","apa":"Tönjes, J., Kell, L., &#38; Werner, T. (2023). Organocatalytic Stereospecific Appel Reaction. <i>Organic Letters</i>, <i>25</i>(51), 9114–9118. <a href=\"https://doi.org/10.1021/acs.orglett.3c03463\">https://doi.org/10.1021/acs.orglett.3c03463</a>","ama":"Tönjes J, Kell L, Werner T. Organocatalytic Stereospecific Appel Reaction. <i>Organic Letters</i>. 2023;25(51):9114-9118. doi:<a href=\"https://doi.org/10.1021/acs.orglett.3c03463\">10.1021/acs.orglett.3c03463</a>","ieee":"J. Tönjes, L. Kell, and T. Werner, “Organocatalytic Stereospecific Appel Reaction,” <i>Organic Letters</i>, vol. 25, no. 51, pp. 9114–9118, 2023, doi: <a href=\"https://doi.org/10.1021/acs.orglett.3c03463\">10.1021/acs.orglett.3c03463</a>.","chicago":"Tönjes, Jan, Lukas Kell, and Thomas Werner. “Organocatalytic Stereospecific Appel Reaction.” <i>Organic Letters</i> 25, no. 51 (2023): 9114–18. <a href=\"https://doi.org/10.1021/acs.orglett.3c03463\">https://doi.org/10.1021/acs.orglett.3c03463</a>."},"publication_identifier":{"issn":["1523-7060","1523-7052"]},"publication_status":"published","issue":"51","title":"Organocatalytic Stereospecific Appel Reaction","doi":"10.1021/acs.orglett.3c03463","publisher":"American Chemical Society (ACS)","date_updated":"2025-11-10T08:46:39Z","volume":25,"author":[{"first_name":"Jan","last_name":"Tönjes","full_name":"Tönjes, Jan"},{"full_name":"Kell, Lukas","last_name":"Kell","first_name":"Lukas"},{"last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271","first_name":"Thomas"}],"date_created":"2025-11-05T15:22:44Z"},{"publication":"Nachrichten aus der Chemie","type":"journal_article","status":"public","_id":"37942","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","keyword":["General Chemical Engineering","General Chemistry"],"language":[{"iso":"eng"}],"publication_identifier":{"issn":["1439-9598","1868-0054"]},"publication_status":"published","issue":"3","year":"2022","page":"42-69","intvolume":"        70","citation":{"mla":"Andexer, Jennifer N., et al. “Trendbericht Organische Chemie 2022.” <i>Nachrichten Aus Der Chemie</i>, vol. 70, no. 3, Wiley, 2022, pp. 42–69, doi:<a href=\"https://doi.org/10.1002/nadc.20224122453\">10.1002/nadc.20224122453</a>.","bibtex":"@article{Andexer_Beifuss_Brasholz_Breinbauer_Breugst_Dumele_Ernst_Ganardi_Giese_Gulder_et al._2022, title={Trendbericht Organische Chemie 2022}, volume={70}, DOI={<a href=\"https://doi.org/10.1002/nadc.20224122453\">10.1002/nadc.20224122453</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Andexer, Jennifer N. and Beifuss, Uwe and Brasholz, Malte and Breinbauer, Rolf and Breugst, Martin and Dumele, Oliver and Ernst, Martin and Ganardi, Ruth and Giese, Michael and Gulder, Tobias A. M. and et al.}, year={2022}, pages={42–69} }","short":"J.N. Andexer, U. Beifuss, M. Brasholz, R. Breinbauer, M. Breugst, O. Dumele, M. Ernst, R. Ganardi, M. Giese, T.A.M. Gulder, W. Hüttel, S. Kath‐Schorr, K. Körber, M. Kordes, T. Lindel, C. Mück‐Lichtenfeld, J. Niemeyer, R. Pfau, F. Pfrengle, J. Pietruszka, J.L. Röckl, N. Schaschke, H. Sebode, M.O. Senge, B.F. Straub, J. Teichert, S.R. Waldvogel, T. Werner, C. Winter, Nachrichten Aus Der Chemie 70 (2022) 42–69.","apa":"Andexer, J. N., Beifuss, U., Brasholz, M., Breinbauer, R., Breugst, M., Dumele, O., Ernst, M., Ganardi, R., Giese, M., Gulder, T. A. M., Hüttel, W., Kath‐Schorr, S., Körber, K., Kordes, M., Lindel, T., Mück‐Lichtenfeld, C., Niemeyer, J., Pfau, R., Pfrengle, F., … Winter, C. (2022). Trendbericht Organische Chemie 2022. <i>Nachrichten Aus Der Chemie</i>, <i>70</i>(3), 42–69. <a href=\"https://doi.org/10.1002/nadc.20224122453\">https://doi.org/10.1002/nadc.20224122453</a>","ama":"Andexer JN, Beifuss U, Brasholz M, et al. Trendbericht Organische Chemie 2022. <i>Nachrichten aus der Chemie</i>. 2022;70(3):42-69. doi:<a href=\"https://doi.org/10.1002/nadc.20224122453\">10.1002/nadc.20224122453</a>","chicago":"Andexer, Jennifer N., Uwe Beifuss, Malte Brasholz, Rolf Breinbauer, Martin Breugst, Oliver Dumele, Martin Ernst, et al. “Trendbericht Organische Chemie 2022.” <i>Nachrichten Aus Der Chemie</i> 70, no. 3 (2022): 42–69. <a href=\"https://doi.org/10.1002/nadc.20224122453\">https://doi.org/10.1002/nadc.20224122453</a>.","ieee":"J. N. Andexer <i>et al.</i>, “Trendbericht Organische Chemie 2022,” <i>Nachrichten aus der Chemie</i>, vol. 70, no. 3, pp. 42–69, 2022, doi: <a href=\"https://doi.org/10.1002/nadc.20224122453\">10.1002/nadc.20224122453</a>."},"date_updated":"2025-11-10T07:59:34Z","publisher":"Wiley","volume":70,"date_created":"2023-01-22T20:22:02Z","author":[{"first_name":"Jennifer N.","full_name":"Andexer, Jennifer N.","last_name":"Andexer"},{"last_name":"Beifuss","full_name":"Beifuss, Uwe","first_name":"Uwe"},{"first_name":"Malte","last_name":"Brasholz","full_name":"Brasholz, Malte"},{"full_name":"Breinbauer, Rolf","last_name":"Breinbauer","first_name":"Rolf"},{"first_name":"Martin","last_name":"Breugst","full_name":"Breugst, Martin"},{"full_name":"Dumele, Oliver","last_name":"Dumele","first_name":"Oliver"},{"first_name":"Martin","full_name":"Ernst, Martin","last_name":"Ernst"},{"last_name":"Ganardi","full_name":"Ganardi, Ruth","first_name":"Ruth"},{"full_name":"Giese, Michael","last_name":"Giese","first_name":"Michael"},{"first_name":"Tobias A. M.","full_name":"Gulder, Tobias A. M.","last_name":"Gulder"},{"last_name":"Hüttel","full_name":"Hüttel, Wolfgang","first_name":"Wolfgang"},{"full_name":"Kath‐Schorr, Stephanie","last_name":"Kath‐Schorr","first_name":"Stephanie"},{"last_name":"Körber","full_name":"Körber, Karsten","first_name":"Karsten"},{"full_name":"Kordes, Markus","last_name":"Kordes","first_name":"Markus"},{"last_name":"Lindel","full_name":"Lindel, Thomas","first_name":"Thomas"},{"full_name":"Mück‐Lichtenfeld, Christian","last_name":"Mück‐Lichtenfeld","first_name":"Christian"},{"full_name":"Niemeyer, Jochen","last_name":"Niemeyer","first_name":"Jochen"},{"last_name":"Pfau","full_name":"Pfau, Roland","first_name":"Roland"},{"first_name":"Fabian","last_name":"Pfrengle","full_name":"Pfrengle, Fabian"},{"first_name":"Jörg","last_name":"Pietruszka","full_name":"Pietruszka, Jörg"},{"full_name":"Röckl, Johannes L.","last_name":"Röckl","first_name":"Johannes L."},{"first_name":"Norbert","last_name":"Schaschke","full_name":"Schaschke, Norbert"},{"first_name":"Hanna","full_name":"Sebode, Hanna","last_name":"Sebode"},{"first_name":"Mathias O.","full_name":"Senge, Mathias O.","last_name":"Senge"},{"last_name":"Straub","full_name":"Straub, Bernd F.","first_name":"Bernd F."},{"last_name":"Teichert","full_name":"Teichert, Johannes","first_name":"Johannes"},{"full_name":"Waldvogel, Siegfried R.","last_name":"Waldvogel","first_name":"Siegfried R."},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner"},{"full_name":"Winter, Christian","last_name":"Winter","first_name":"Christian"}],"title":"Trendbericht Organische Chemie 2022","doi":"10.1002/nadc.20224122453"},{"status":"public","type":"journal_article","_id":"37938","user_id":"89271","department":[{"_id":"2"},{"_id":"657"}],"citation":{"short":"C. Terazzi, K. Laatz, J. von Langermann, T. Werner, ACS Sustainable Chemistry and Engineering 10 (2022) 13335–13342.","bibtex":"@article{Terazzi_Laatz_von Langermann_Werner_2022, title={Synthesis of Cyclic Carbonates Catalyzed by CaI<sub>2</sub>–Et<sub>3</sub>N and Studies on Their Biocatalytic Kinetic Resolution}, volume={10}, DOI={<a href=\"https://doi.org/10.1021/acssuschemeng.2c03210\">10.1021/acssuschemeng.2c03210</a>}, number={40}, journal={ACS Sustainable Chemistry and Engineering}, publisher={American Chemical Society (ACS)}, author={Terazzi, Constanza and Laatz, Karoline and von Langermann, Jan and Werner, Thomas}, year={2022}, pages={13335–13342} }","mla":"Terazzi, Constanza, et al. “Synthesis of Cyclic Carbonates Catalyzed by CaI<sub>2</sub>–Et<sub>3</sub>N and Studies on Their Biocatalytic Kinetic Resolution.” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 10, no. 40, American Chemical Society (ACS), 2022, pp. 13335–42, doi:<a href=\"https://doi.org/10.1021/acssuschemeng.2c03210\">10.1021/acssuschemeng.2c03210</a>.","apa":"Terazzi, C., Laatz, K., von Langermann, J., &#38; Werner, T. (2022). Synthesis of Cyclic Carbonates Catalyzed by CaI<sub>2</sub>–Et<sub>3</sub>N and Studies on Their Biocatalytic Kinetic Resolution. <i>ACS Sustainable Chemistry and Engineering</i>, <i>10</i>(40), 13335–13342. <a href=\"https://doi.org/10.1021/acssuschemeng.2c03210\">https://doi.org/10.1021/acssuschemeng.2c03210</a>","chicago":"Terazzi, Constanza, Karoline Laatz, Jan von Langermann, and Thomas Werner. “Synthesis of Cyclic Carbonates Catalyzed by CaI<sub>2</sub>–Et<sub>3</sub>N and Studies on Their Biocatalytic Kinetic Resolution.” <i>ACS Sustainable Chemistry and Engineering</i> 10, no. 40 (2022): 13335–42. <a href=\"https://doi.org/10.1021/acssuschemeng.2c03210\">https://doi.org/10.1021/acssuschemeng.2c03210</a>.","ieee":"C. Terazzi, K. Laatz, J. von Langermann, and T. Werner, “Synthesis of Cyclic Carbonates Catalyzed by CaI<sub>2</sub>–Et<sub>3</sub>N and Studies on Their Biocatalytic Kinetic Resolution,” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 10, no. 40, pp. 13335–13342, 2022, doi: <a href=\"https://doi.org/10.1021/acssuschemeng.2c03210\">10.1021/acssuschemeng.2c03210</a>.","ama":"Terazzi C, Laatz K, von Langermann J, Werner T. Synthesis of Cyclic Carbonates Catalyzed by CaI<sub>2</sub>–Et<sub>3</sub>N and Studies on Their Biocatalytic Kinetic Resolution. <i>ACS Sustainable Chemistry and Engineering</i>. 2022;10(40):13335-13342. doi:<a href=\"https://doi.org/10.1021/acssuschemeng.2c03210\">10.1021/acssuschemeng.2c03210</a>"},"page":"13335-13342","intvolume":"        10","publication_status":"published","publication_identifier":{"issn":["2168-0485","2168-0485"]},"doi":"10.1021/acssuschemeng.2c03210","date_updated":"2025-11-10T08:47:07Z","author":[{"last_name":"Terazzi","full_name":"Terazzi, Constanza","first_name":"Constanza"},{"first_name":"Karoline","last_name":"Laatz","full_name":"Laatz, Karoline"},{"last_name":"von Langermann","full_name":"von Langermann, Jan","first_name":"Jan"},{"last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"volume":10,"publication":"ACS Sustainable Chemistry and Engineering","keyword":["T1","T3","CSSD"],"language":[{"iso":"eng"}],"year":"2022","issue":"40","title":"Synthesis of Cyclic Carbonates Catalyzed by CaI<sub>2</sub>–Et<sub>3</sub>N and Studies on Their Biocatalytic Kinetic Resolution","publisher":"American Chemical Society (ACS)","date_created":"2023-01-22T20:10:44Z"},{"status":"public","type":"journal_article","publication":"Asian Journal of Organic Chemistry","language":[{"iso":"eng"}],"keyword":["T1","T2","CSSD"],"user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37940","citation":{"chicago":"Ren, Changyue, Anke Spannenberg, and Thomas Werner. “Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO            <sub>2</sub>.” <i>Asian Journal of Organic Chemistry</i> 11, no. 9 (2022). <a href=\"https://doi.org/10.1002/ajoc.202200156\">https://doi.org/10.1002/ajoc.202200156</a>.","ieee":"C. Ren, A. Spannenberg, and T. Werner, “Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO            <sub>2</sub>,” <i>Asian Journal of Organic Chemistry</i>, vol. 11, no. 9, 2022, doi: <a href=\"https://doi.org/10.1002/ajoc.202200156\">10.1002/ajoc.202200156</a>.","ama":"Ren C, Spannenberg A, Werner T. Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO            <sub>2</sub>. <i>Asian Journal of Organic Chemistry</i>. 2022;11(9). doi:<a href=\"https://doi.org/10.1002/ajoc.202200156\">10.1002/ajoc.202200156</a>","apa":"Ren, C., Spannenberg, A., &#38; Werner, T. (2022). Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO            <sub>2</sub>. <i>Asian Journal of Organic Chemistry</i>, <i>11</i>(9). <a href=\"https://doi.org/10.1002/ajoc.202200156\">https://doi.org/10.1002/ajoc.202200156</a>","mla":"Ren, Changyue, et al. “Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO            <sub>2</sub>.” <i>Asian Journal of Organic Chemistry</i>, vol. 11, no. 9, Wiley, 2022, doi:<a href=\"https://doi.org/10.1002/ajoc.202200156\">10.1002/ajoc.202200156</a>.","bibtex":"@article{Ren_Spannenberg_Werner_2022, title={Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO            <sub>2</sub>}, volume={11}, DOI={<a href=\"https://doi.org/10.1002/ajoc.202200156\">10.1002/ajoc.202200156</a>}, number={9}, journal={Asian Journal of Organic Chemistry}, publisher={Wiley}, author={Ren, Changyue and Spannenberg, Anke and Werner, Thomas}, year={2022} }","short":"C. Ren, A. Spannenberg, T. Werner, Asian Journal of Organic Chemistry 11 (2022)."},"intvolume":"        11","year":"2022","issue":"9","publication_status":"published","publication_identifier":{"issn":["2193-5807","2193-5815"]},"doi":"10.1002/ajoc.202200156","title":"Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO            <sub>2</sub>","author":[{"full_name":"Ren, Changyue","last_name":"Ren","first_name":"Changyue"},{"first_name":"Anke","full_name":"Spannenberg, Anke","last_name":"Spannenberg"},{"full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"date_created":"2023-01-22T20:19:21Z","volume":11,"publisher":"Wiley","date_updated":"2025-11-10T08:47:20Z"},{"status":"public","type":"patent","department":[{"_id":"35"},{"_id":"2"}],"user_id":"89271","_id":"62144","publication_date":"2022-10-27","citation":{"apa":"Weber, A., Werner, T., Grandane, A., Stefanow, V., &#38; Lenz, O. (2022). <i>Verfahren zur Herstellung von Cedrendiol</i>.","bibtex":"@article{Weber_Werner_Grandane_Stefanow_Lenz_2022, title={Verfahren zur Herstellung von Cedrendiol}, author={Weber, Arne and Werner, Thomas and Grandane, Aiga and Stefanow, V. and Lenz, O.}, year={2022} }","mla":"Weber, Arne, et al. <i>Verfahren Zur Herstellung von Cedrendiol</i>. 2022.","short":"A. Weber, T. Werner, A. Grandane, V. Stefanow, O. Lenz, (2022).","ama":"Weber A, Werner T, Grandane A, Stefanow V, Lenz O. Verfahren zur Herstellung von Cedrendiol. Published online 2022.","chicago":"Weber, Arne, Thomas Werner, Aiga Grandane, V. Stefanow, and O. Lenz. “Verfahren Zur Herstellung von Cedrendiol,” 2022.","ieee":"A. Weber, T. Werner, A. Grandane, V. Stefanow, and O. Lenz, “Verfahren zur Herstellung von Cedrendiol.” 2022."},"year":"2022","application_number":"WO2022/223117 A1","title":"Verfahren zur Herstellung von Cedrendiol","ipn":"WO2022/223117 A1","date_created":"2025-11-10T07:55:33Z","author":[{"first_name":"Arne","last_name":"Weber","full_name":"Weber, Arne"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas"},{"first_name":"Aiga","last_name":"Grandane","full_name":"Grandane, Aiga"},{"last_name":"Stefanow","full_name":"Stefanow, V.","first_name":"V."},{"last_name":"Lenz","full_name":"Lenz, O.","first_name":"O."}],"ipc":"-","date_updated":"2025-11-10T09:48:50Z"},{"publisher":"Wiley","date_updated":"2025-11-10T08:02:44Z","volume":69,"author":[{"first_name":"Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies","id":"53339","full_name":"Paradies, Jan"},{"first_name":"Jennifer","last_name":"Andexer","full_name":"Andexer, Jennifer"},{"last_name":"Beifuss","full_name":"Beifuss, Uwe","first_name":"Uwe"},{"last_name":"Beuerle","full_name":"Beuerle, Florian","first_name":"Florian"},{"full_name":"Brasholz, Malte","last_name":"Brasholz","first_name":"Malte"},{"first_name":"Rolf","last_name":"Breinbauer","full_name":"Breinbauer, Rolf"},{"first_name":"Martin","full_name":"Ernst, Martin","last_name":"Ernst"},{"full_name":"Ganardi, Ruth","last_name":"Ganardi","first_name":"Ruth"},{"first_name":"Tobias A. M.","last_name":"Gulder","full_name":"Gulder, Tobias A. M."},{"full_name":"Hüttel, Wolfgang","last_name":"Hüttel","first_name":"Wolfgang"},{"last_name":"Kath‐Schorr","full_name":"Kath‐Schorr, Stephanie","first_name":"Stephanie"},{"first_name":"Karsten","last_name":"Körber","full_name":"Körber, Karsten"},{"first_name":"Markus","full_name":"Kordes, Markus","last_name":"Kordes"},{"last_name":"Lehmann","full_name":"Lehmann, Matthias","first_name":"Matthias"},{"full_name":"Lindel, Thomas","last_name":"Lindel","first_name":"Thomas"},{"last_name":"Luy","full_name":"Luy, Burkhard","first_name":"Burkhard"},{"full_name":"Mück‐Lichtenfeld, Christian","last_name":"Mück‐Lichtenfeld","first_name":"Christian"},{"first_name":"Claudia","full_name":"Muhle‐Goll, Claudia","last_name":"Muhle‐Goll"},{"first_name":"Jochen","last_name":"Niemeyer","full_name":"Niemeyer, Jochen"},{"last_name":"Pfau","full_name":"Pfau, Roland","first_name":"Roland"},{"last_name":"Pietruszka","full_name":"Pietruszka, Jörg","first_name":"Jörg"},{"first_name":"Johannes L.","full_name":"Röckl, Johannes L.","last_name":"Röckl"},{"last_name":"Schaschke","full_name":"Schaschke, Norbert","first_name":"Norbert"},{"first_name":"Mathias O.","last_name":"Senge","full_name":"Senge, Mathias O."},{"last_name":"Straub","full_name":"Straub, Bernd F.","first_name":"Bernd F."},{"first_name":"Siegfried R.","full_name":"Waldvogel, Siegfried R.","last_name":"Waldvogel"},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244"},{"full_name":"Werz, Daniel B.","last_name":"Werz","first_name":"Daniel B."},{"last_name":"Winter","full_name":"Winter, Christian","first_name":"Christian"}],"date_created":"2023-01-22T20:28:35Z","title":"Organische Chemie","doi":"10.1002/nadc.20214105947","publication_identifier":{"issn":["1439-9598","1868-0054"]},"publication_status":"published","issue":"3","year":"2021","intvolume":"        69","page":"38-68","citation":{"apa":"Paradies, J., Andexer, J., Beifuss, U., Beuerle, F., Brasholz, M., Breinbauer, R., Ernst, M., Ganardi, R., Gulder, T. A. M., Hüttel, W., Kath‐Schorr, S., Körber, K., Kordes, M., Lehmann, M., Lindel, T., Luy, B., Mück‐Lichtenfeld, C., Muhle‐Goll, C., Niemeyer, J., … Winter, C. (2021). Organische Chemie. <i>Nachrichten Aus Der Chemie</i>, <i>69</i>(3), 38–68. <a href=\"https://doi.org/10.1002/nadc.20214105947\">https://doi.org/10.1002/nadc.20214105947</a>","mla":"Paradies, Jan, et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i>, vol. 69, no. 3, Wiley, 2021, pp. 38–68, doi:<a href=\"https://doi.org/10.1002/nadc.20214105947\">10.1002/nadc.20214105947</a>.","short":"J. Paradies, J. Andexer, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, M. Ernst, R. Ganardi, T.A.M. Gulder, W. Hüttel, S. Kath‐Schorr, K. Körber, M. Kordes, M. Lehmann, T. Lindel, B. Luy, C. Mück‐Lichtenfeld, C. Muhle‐Goll, J. Niemeyer, R. Pfau, J. Pietruszka, J.L. Röckl, N. Schaschke, M.O. Senge, B.F. Straub, S.R. Waldvogel, T. Werner, D.B. Werz, C. Winter, Nachrichten Aus Der Chemie 69 (2021) 38–68.","bibtex":"@article{Paradies_Andexer_Beifuss_Beuerle_Brasholz_Breinbauer_Ernst_Ganardi_Gulder_Hüttel_et al._2021, title={Organische Chemie}, volume={69}, DOI={<a href=\"https://doi.org/10.1002/nadc.20214105947\">10.1002/nadc.20214105947</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Paradies, Jan and Andexer, Jennifer and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ernst, Martin and Ganardi, Ruth and Gulder, Tobias A. M. and Hüttel, Wolfgang and et al.}, year={2021}, pages={38–68} }","ama":"Paradies J, Andexer J, Beifuss U, et al. Organische Chemie. <i>Nachrichten aus der Chemie</i>. 2021;69(3):38-68. doi:<a href=\"https://doi.org/10.1002/nadc.20214105947\">10.1002/nadc.20214105947</a>","ieee":"J. Paradies <i>et al.</i>, “Organische Chemie,” <i>Nachrichten aus der Chemie</i>, vol. 69, no. 3, pp. 38–68, 2021, doi: <a href=\"https://doi.org/10.1002/nadc.20214105947\">10.1002/nadc.20214105947</a>.","chicago":"Paradies, Jan, Jennifer Andexer, Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, Martin Ernst, et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i> 69, no. 3 (2021): 38–68. <a href=\"https://doi.org/10.1002/nadc.20214105947\">https://doi.org/10.1002/nadc.20214105947</a>."},"_id":"37947","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","keyword":["General Chemical Engineering","General Chemistry"],"language":[{"iso":"eng"}],"publication":"Nachrichten aus der Chemie","type":"journal_article","status":"public"},{"publisher":"Wiley","date_created":"2023-01-22T20:34:17Z","title":"Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts","issue":"1","year":"2021","keyword":["T1"],"language":[{"iso":"eng"}],"publication":"ChemSusChem","date_updated":"2025-11-10T08:04:27Z","author":[{"first_name":"Yuya","last_name":"Hu","full_name":"Hu, Yuya"},{"last_name":"Wei","full_name":"Wei, Zhihong","first_name":"Zhihong"},{"first_name":"Anna","full_name":"Frey, Anna","last_name":"Frey"},{"last_name":"Kubis","full_name":"Kubis, Christoph","first_name":"Christoph"},{"last_name":"Ren","full_name":"Ren, Chang‐Yue","first_name":"Chang‐Yue"},{"first_name":"Anke","full_name":"Spannenberg, Anke","last_name":"Spannenberg"},{"first_name":"Haijun","last_name":"Jiao","full_name":"Jiao, Haijun"},{"orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271","first_name":"Thomas"}],"volume":14,"doi":"10.1002/cssc.202002267","publication_status":"published","publication_identifier":{"issn":["1864-5631","1864-564X"]},"citation":{"apa":"Hu, Y., Wei, Z., Frey, A., Kubis, C., Ren, C., Spannenberg, A., Jiao, H., &#38; Werner, T. (2021). Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts. <i>ChemSusChem</i>, <i>14</i>(1), 363–372. <a href=\"https://doi.org/10.1002/cssc.202002267\">https://doi.org/10.1002/cssc.202002267</a>","bibtex":"@article{Hu_Wei_Frey_Kubis_Ren_Spannenberg_Jiao_Werner_2021, title={Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts}, volume={14}, DOI={<a href=\"https://doi.org/10.1002/cssc.202002267\">10.1002/cssc.202002267</a>}, number={1}, journal={ChemSusChem}, publisher={Wiley}, author={Hu, Yuya and Wei, Zhihong and Frey, Anna and Kubis, Christoph and Ren, Chang‐Yue and Spannenberg, Anke and Jiao, Haijun and Werner, Thomas}, year={2021}, pages={363–372} }","short":"Y. Hu, Z. Wei, A. Frey, C. Kubis, C. Ren, A. Spannenberg, H. Jiao, T. Werner, ChemSusChem 14 (2021) 363–372.","mla":"Hu, Yuya, et al. “Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts.” <i>ChemSusChem</i>, vol. 14, no. 1, Wiley, 2021, pp. 363–72, doi:<a href=\"https://doi.org/10.1002/cssc.202002267\">10.1002/cssc.202002267</a>.","ieee":"Y. Hu <i>et al.</i>, “Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts,” <i>ChemSusChem</i>, vol. 14, no. 1, pp. 363–372, 2021, doi: <a href=\"https://doi.org/10.1002/cssc.202002267\">10.1002/cssc.202002267</a>.","chicago":"Hu, Yuya, Zhihong Wei, Anna Frey, Christoph Kubis, Chang‐Yue Ren, Anke Spannenberg, Haijun Jiao, and Thomas Werner. “Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts.” <i>ChemSusChem</i> 14, no. 1 (2021): 363–72. <a href=\"https://doi.org/10.1002/cssc.202002267\">https://doi.org/10.1002/cssc.202002267</a>.","ama":"Hu Y, Wei Z, Frey A, et al. Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts. <i>ChemSusChem</i>. 2021;14(1):363-372. doi:<a href=\"https://doi.org/10.1002/cssc.202002267\">10.1002/cssc.202002267</a>"},"page":"363-372","intvolume":"        14","_id":"37950","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"extern":"1","type":"journal_article","status":"public"},{"title":"Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones","doi":"10.1055/a-1509-6078","date_updated":"2025-11-10T08:47:47Z","publisher":"Georg Thieme Verlag KG","volume":53,"date_created":"2023-01-22T20:27:34Z","author":[{"orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"},{"first_name":"Aiga","last_name":"Grandane","full_name":"Grandane, Aiga"},{"first_name":"Linda","full_name":"Pudnika, Linda","last_name":"Pudnika"},{"last_name":"Domraceva","full_name":"Domraceva, Ilona","first_name":"Ilona"},{"first_name":"Raivis","full_name":"Zalubovskis, Raivis","last_name":"Zalubovskis"}],"year":"2021","page":"3545-3554","intvolume":"        53","citation":{"ama":"Werner T, Grandane A, Pudnika L, Domraceva I, Zalubovskis R. Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones. <i>Synthesis</i>. 2021;53(19):3545-3554. doi:<a href=\"https://doi.org/10.1055/a-1509-6078\">10.1055/a-1509-6078</a>","chicago":"Werner, Thomas, Aiga Grandane, Linda Pudnika, Ilona Domraceva, and Raivis Zalubovskis. “Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones.” <i>Synthesis</i> 53, no. 19 (2021): 3545–54. <a href=\"https://doi.org/10.1055/a-1509-6078\">https://doi.org/10.1055/a-1509-6078</a>.","ieee":"T. Werner, A. Grandane, L. Pudnika, I. Domraceva, and R. Zalubovskis, “Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones,” <i>Synthesis</i>, vol. 53, no. 19, pp. 3545–3554, 2021, doi: <a href=\"https://doi.org/10.1055/a-1509-6078\">10.1055/a-1509-6078</a>.","apa":"Werner, T., Grandane, A., Pudnika, L., Domraceva, I., &#38; Zalubovskis, R. (2021). Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones. <i>Synthesis</i>, <i>53</i>(19), 3545–3554. <a href=\"https://doi.org/10.1055/a-1509-6078\">https://doi.org/10.1055/a-1509-6078</a>","short":"T. Werner, A. Grandane, L. Pudnika, I. Domraceva, R. Zalubovskis, Synthesis 53 (2021) 3545–3554.","mla":"Werner, Thomas, et al. “Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones.” <i>Synthesis</i>, vol. 53, no. 19, Georg Thieme Verlag KG, 2021, pp. 3545–54, doi:<a href=\"https://doi.org/10.1055/a-1509-6078\">10.1055/a-1509-6078</a>.","bibtex":"@article{Werner_Grandane_Pudnika_Domraceva_Zalubovskis_2021, title={Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones}, volume={53}, DOI={<a href=\"https://doi.org/10.1055/a-1509-6078\">10.1055/a-1509-6078</a>}, number={19}, journal={Synthesis}, publisher={Georg Thieme Verlag KG}, author={Werner, Thomas and Grandane, Aiga and Pudnika, Linda and Domraceva, Ilona and Zalubovskis, Raivis}, year={2021}, pages={3545–3554} }"},"publication_identifier":{"issn":["0039-7881","1437-210X"]},"publication_status":"published","issue":"19","keyword":["T2","T4","CSSD"],"language":[{"iso":"eng"}],"_id":"37946","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>The facile synthesis of highly functionalized building blocks with potential biological activity is of great interest to medicinal chemistry. The benzoxepinone core structures commonly exhibit biological activity. Thus, a short and efficient synthetic route towards benzoxepine containing scaffold, which enables late stage modification was developed. Namely, base-free catalytic Wittig reactions enabled the synthesis of bromobenzoxepinones from readily available starting materials. Subsequent, Suzuki–Miyaura and Stille reactions proved to be suitable methods to access a variety of benzoxepinone diaryl derivatives by late stage modification in only three steps. This three-step reaction sequence is suitable for high throughput applications and gives facile access to highly complex molecular structures, which are suitable for further functionalization. The antiproliferative properties of selected arylbenzoxepinones­ were tested in vitro on monolayer tumor cell line A549. Notably, in this initial screening, these compounds were found to be active in the micromolar range.</jats:p>","lang":"eng"}],"status":"public","publication":"Synthesis","type":"journal_article"},{"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37944","language":[{"iso":"eng"}],"keyword":["T1","T3","CSSD"],"publication":"Chemical Science","type":"journal_article","status":"public","abstract":[{"lang":"eng","text":"<p>A Mn–PNP complex proved to be a suitable catalyst for the transfer hydrogenation of amides, carbamates, urea derivatives and even polyurethanes.</p>"}],"volume":12,"author":[{"last_name":"Liu","full_name":"Liu, Xin","first_name":"Xin"},{"orcid":"https://orcid.org/0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"date_created":"2023-01-22T20:24:03Z","date_updated":"2025-11-10T08:49:01Z","publisher":"Royal Society of Chemistry (RSC)","doi":"10.1039/d1sc02663a","title":"Indirect reduction of CO<sub>2</sub> and recycling of polymers by manganese-catalyzed transfer hydrogenation of amides, carbamates, urea derivatives, and polyurethanes","issue":"31","publication_identifier":{"issn":["2041-6520","2041-6539"]},"publication_status":"published","page":"10590-10597","intvolume":"        12","citation":{"apa":"Liu, X., &#38; Werner, T. (2021). Indirect reduction of CO<sub>2</sub> and recycling of polymers by manganese-catalyzed transfer hydrogenation of amides, carbamates, urea derivatives, and polyurethanes. <i>Chemical Science</i>, <i>12</i>(31), 10590–10597. <a href=\"https://doi.org/10.1039/d1sc02663a\">https://doi.org/10.1039/d1sc02663a</a>","short":"X. Liu, T. Werner, Chemical Science 12 (2021) 10590–10597.","mla":"Liu, Xin, and Thomas Werner. “Indirect Reduction of CO<sub>2</sub> and Recycling of Polymers by Manganese-Catalyzed Transfer Hydrogenation of Amides, Carbamates, Urea Derivatives, and Polyurethanes.” <i>Chemical Science</i>, vol. 12, no. 31, Royal Society of Chemistry (RSC), 2021, pp. 10590–97, doi:<a href=\"https://doi.org/10.1039/d1sc02663a\">10.1039/d1sc02663a</a>.","bibtex":"@article{Liu_Werner_2021, title={Indirect reduction of CO<sub>2</sub> and recycling of polymers by manganese-catalyzed transfer hydrogenation of amides, carbamates, urea derivatives, and polyurethanes}, volume={12}, DOI={<a href=\"https://doi.org/10.1039/d1sc02663a\">10.1039/d1sc02663a</a>}, number={31}, journal={Chemical Science}, publisher={Royal Society of Chemistry (RSC)}, author={Liu, Xin and Werner, Thomas}, year={2021}, pages={10590–10597} }","chicago":"Liu, Xin, and Thomas Werner. “Indirect Reduction of CO<sub>2</sub> and Recycling of Polymers by Manganese-Catalyzed Transfer Hydrogenation of Amides, Carbamates, Urea Derivatives, and Polyurethanes.” <i>Chemical Science</i> 12, no. 31 (2021): 10590–97. <a href=\"https://doi.org/10.1039/d1sc02663a\">https://doi.org/10.1039/d1sc02663a</a>.","ieee":"X. Liu and T. Werner, “Indirect reduction of CO<sub>2</sub> and recycling of polymers by manganese-catalyzed transfer hydrogenation of amides, carbamates, urea derivatives, and polyurethanes,” <i>Chemical Science</i>, vol. 12, no. 31, pp. 10590–10597, 2021, doi: <a href=\"https://doi.org/10.1039/d1sc02663a\">10.1039/d1sc02663a</a>.","ama":"Liu X, Werner T. Indirect reduction of CO<sub>2</sub> and recycling of polymers by manganese-catalyzed transfer hydrogenation of amides, carbamates, urea derivatives, and polyurethanes. <i>Chemical Science</i>. 2021;12(31):10590-10597. doi:<a href=\"https://doi.org/10.1039/d1sc02663a\">10.1039/d1sc02663a</a>"},"year":"2021"}]