--- _id: '37970' author: - first_name: Lars full_name: Longwitz, Lars last_name: Longwitz - first_name: Johannes full_name: Steinbauer, Johannes last_name: Steinbauer - first_name: Anke full_name: Spannenberg, Anke last_name: Spannenberg - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: https://orcid.org/0000-0001-9025-3244 citation: ama: Longwitz L, Steinbauer J, Spannenberg A, Werner T. Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions. ACS Catalysis. 2017;8(1):665-672. doi:10.1021/acscatal.7b03367 apa: Longwitz, L., Steinbauer, J., Spannenberg, A., & Werner, T. (2017). Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions. ACS Catalysis, 8(1), 665–672. https://doi.org/10.1021/acscatal.7b03367 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={10.1021/acscatal.7b03367}, 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} }' 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.” ACS Catalysis 8, no. 1 (2017): 665–72. https://doi.org/10.1021/acscatal.7b03367.' 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,” ACS Catalysis, vol. 8, no. 1, pp. 665–672, 2017, doi: 10.1021/acscatal.7b03367.' mla: Longwitz, Lars, et al. “Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions.” ACS Catalysis, vol. 8, no. 1, American Chemical Society (ACS), 2017, pp. 665–72, doi:10.1021/acscatal.7b03367. short: L. Longwitz, J. Steinbauer, A. Spannenberg, T. Werner, ACS Catalysis 8 (2017) 665–672. date_created: 2023-01-22T20:47:19Z date_updated: 2025-11-06T08:38:07Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1021/acscatal.7b03367 extern: '1' intvolume: ' 8' issue: '1' keyword: - T1 - T3 - T4 language: - iso: eng page: 665-672 publication: ACS Catalysis publication_identifier: issn: - 2155-5435 - 2155-5435 publication_status: published publisher: American Chemical Society (ACS) status: public title: Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions type: journal_article user_id: '89271' volume: 8 year: '2017' ... --- _id: '37979' author: - first_name: Bernd F. full_name: Straub, Bernd F. last_name: Straub - first_name: Jennifer full_name: Andexer, Jennifer last_name: Andexer - first_name: Christoph full_name: Arenz, Christoph last_name: Arenz - first_name: Uwe full_name: Beifuss, Uwe last_name: Beifuss - first_name: Florian full_name: Beuerle, Florian last_name: Beuerle - first_name: Malte full_name: Brasholz, Malte last_name: Brasholz - first_name: Rolf full_name: Breinbauer, Rolf last_name: Breinbauer - first_name: Klaus full_name: Ditrich, Klaus last_name: Ditrich - first_name: Tobias A. M. full_name: Gulder, Tobias A. M. last_name: Gulder - first_name: Wolfgang full_name: Hüttel, Wolfgang last_name: Hüttel - first_name: Markus full_name: Kordes, Markus last_name: Kordes - first_name: Anke full_name: Krueger, Anke last_name: Krueger - first_name: Matthias full_name: Lehmann, Matthias last_name: Lehmann - first_name: Thomas full_name: Lindel, Thomas last_name: Lindel - first_name: Burkhard full_name: Luy, Burkhard last_name: Luy - first_name: Michael A. R. full_name: Meier, Michael A. R. last_name: Meier - first_name: Christian full_name: Mück-Lichtenfeld, Christian last_name: Mück-Lichtenfeld - first_name: Claudia full_name: Muhle-Goll, Claudia last_name: Muhle-Goll - first_name: Thomas J. J. full_name: Müller, Thomas J. J. last_name: Müller - first_name: Arun full_name: Narine, Arun last_name: Narine - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X - first_name: Roland full_name: Pfau, Roland last_name: Pfau - first_name: Jörg full_name: Pietruszka, Jörg last_name: Pietruszka - first_name: Norbert full_name: Schaschke, Norbert last_name: Schaschke - first_name: Mathias O. full_name: Senge, Mathias O. last_name: Senge - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: 0000-0001-9025-3244 - first_name: Daniel B. full_name: Werz, Daniel B. last_name: Werz - first_name: Christian A. full_name: Winter, Christian A. last_name: Winter - first_name: Dennis full_name: Worgull, Dennis last_name: Worgull citation: ama: Straub BF, Andexer J, Arenz C, et al. Organische Chemie 2016. Nachrichten aus der Chemie. 2017;65(3):266-304. doi:10.1002/nadc.20174059831 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. Nachrichten Aus Der Chemie, 65(3), 266–304. https://doi.org/10.1002/nadc.20174059831 bibtex: '@article{Straub_Andexer_Arenz_Beifuss_Beuerle_Brasholz_Breinbauer_Ditrich_Gulder_Hüttel_et al._2017, title={Organische Chemie 2016}, volume={65}, DOI={10.1002/nadc.20174059831}, 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} }' chicago: 'Straub, Bernd F., Jennifer Andexer, Christoph Arenz, Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, et al. “Organische Chemie 2016.” Nachrichten Aus Der Chemie 65, no. 3 (2017): 266–304. https://doi.org/10.1002/nadc.20174059831.' ieee: 'B. F. Straub et al., “Organische Chemie 2016,” Nachrichten aus der Chemie, vol. 65, no. 3, pp. 266–304, 2017, doi: 10.1002/nadc.20174059831.' mla: Straub, Bernd F., et al. “Organische Chemie 2016.” Nachrichten Aus Der Chemie, vol. 65, no. 3, Wiley, 2017, pp. 266–304, doi:10.1002/nadc.20174059831. 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. date_created: 2023-01-22T21:00:37Z date_updated: 2025-11-10T09:11:28Z department: - _id: '35' - _id: '2' - _id: '657' - _id: '389' doi: 10.1002/nadc.20174059831 extern: '1' intvolume: ' 65' issue: '3' keyword: - General Chemical Engineering - General Chemistry language: - iso: eng page: 266-304 publication: Nachrichten aus der Chemie publication_identifier: issn: - 1439-9598 publication_status: published publisher: Wiley status: public title: Organische Chemie 2016 type: journal_article user_id: '89271' volume: 65 year: '2017' ... --- _id: '37976' author: - first_name: Wu full_name: Li, Wu last_name: Li - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: 0000-0001-9025-3244 citation: ama: 'Li W, Werner T. B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles. Organic Letters. 2017;19(10):2568-2571. doi:10.1021/acs.orglett.7b00720' apa: 'Li, W., & Werner, T. (2017). B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles. Organic Letters, 19(10), 2568–2571. https://doi.org/10.1021/acs.orglett.7b00720' bibtex: '@article{Li_Werner_2017, title={B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles}, volume={19}, DOI={10.1021/acs.orglett.7b00720}, number={10}, journal={Organic Letters}, publisher={American Chemical Society (ACS)}, author={Li, Wu and Werner, Thomas}, year={2017}, pages={2568–2571} }' chicago: 'Li, Wu, and Thomas Werner. “B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles.” Organic Letters 19, no. 10 (2017): 2568–71. https://doi.org/10.1021/acs.orglett.7b00720.' ieee: 'W. Li and T. Werner, “B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles,” Organic Letters, vol. 19, no. 10, pp. 2568–2571, 2017, doi: 10.1021/acs.orglett.7b00720.' mla: 'Li, Wu, and Thomas Werner. “B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles.” Organic Letters, vol. 19, no. 10, American Chemical Society (ACS), 2017, pp. 2568–71, doi:10.1021/acs.orglett.7b00720.' short: W. Li, T. Werner, Organic Letters 19 (2017) 2568–2571. date_created: 2023-01-22T20:59:34Z date_updated: 2025-11-10T09:14:45Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1021/acs.orglett.7b00720 extern: '1' intvolume: ' 19' issue: '10' keyword: - CSSD language: - iso: eng page: 2568-2571 publication: Organic Letters publication_identifier: issn: - 1523-7060 - 1523-7052 publication_status: published publisher: American Chemical Society (ACS) status: public title: 'B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles' type: journal_article user_id: '89271' volume: 19 year: '2017' ... --- _id: '37973' abstract: - lang: eng text:

An immobilized bifunctional phosphonium salt catalyst efficiently catalyzed the synthesis of cyclic carbonates under mild conditions, and was reused up to 15 times.

author: - first_name: J. full_name: Steinbauer, J. last_name: Steinbauer - first_name: L. full_name: Longwitz, L. last_name: Longwitz - first_name: M. full_name: Frank, M. last_name: Frank - first_name: J. full_name: Epping, J. last_name: Epping - first_name: U. full_name: Kragl, U. last_name: Kragl - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: 0000-0001-9025-3244 citation: ama: Steinbauer J, Longwitz L, Frank M, Epping J, Kragl U, Werner T. Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO₂ and epoxides. Green Chemistry. 2017;19(18):4435-4445. doi:10.1039/c7gc01782k apa: Steinbauer, J., Longwitz, L., Frank, M., Epping, J., Kragl, U., & Werner, T. (2017). Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO₂ and epoxides. Green Chemistry, 19(18), 4435–4445. https://doi.org/10.1039/c7gc01782k bibtex: '@article{Steinbauer_Longwitz_Frank_Epping_Kragl_Werner_2017, title={Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO₂ and epoxides}, volume={19}, DOI={10.1039/c7gc01782k}, 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} }' 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 CO₂ and Epoxides.” Green Chemistry 19, no. 18 (2017): 4435–45. https://doi.org/10.1039/c7gc01782k.' ieee: 'J. Steinbauer, L. Longwitz, M. Frank, J. Epping, U. Kragl, and T. Werner, “Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO₂ and epoxides,” Green Chemistry, vol. 19, no. 18, pp. 4435–4445, 2017, doi: 10.1039/c7gc01782k.' mla: Steinbauer, J., et al. “Immobilized Bifunctional Phosphonium Salts as Recyclable Organocatalysts in the Cycloaddition of CO₂ and Epoxides.” Green Chemistry, vol. 19, no. 18, Royal Society of Chemistry (RSC), 2017, pp. 4435–45, doi:10.1039/c7gc01782k. short: J. Steinbauer, L. Longwitz, M. Frank, J. Epping, U. Kragl, T. Werner, Green Chemistry 19 (2017) 4435–4445. date_created: 2023-01-22T20:57:38Z date_updated: 2025-11-10T09:18:10Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1039/c7gc01782k extern: '1' intvolume: ' 19' issue: '18' keyword: - T1 - T2 - CSSD language: - iso: eng page: 4435-4445 publication: Green Chemistry publication_identifier: issn: - 1463-9262 - 1463-9270 publication_status: published publisher: Royal Society of Chemistry (RSC) status: public title: Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO₂ and epoxides type: journal_article user_id: '89271' volume: 19 year: '2017' ... --- _id: '37975' abstract: - lang: eng text: '

Calcium punched beyond its weight: An in situ formed Ca²⁺–crown ether complex showed unprecedented efficiency in cyclic carbonate synthesis.

' author: - first_name: J. full_name: Steinbauer, J. last_name: Steinbauer - first_name: A. full_name: Spannenberg, A. last_name: Spannenberg - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: 0000-0001-9025-3244 citation: ama: Steinbauer J, Spannenberg A, Werner T. An in situ formed Ca²⁺–crown ether complex and its use in CO₂-fixation reactions with terminal and internal epoxides. Green Chemistry. 2017;19(16):3769-3779. doi:10.1039/c7gc01114h apa: Steinbauer, J., Spannenberg, A., & Werner, T. (2017). An in situ formed Ca²⁺–crown ether complex and its use in CO₂-fixation reactions with terminal and internal epoxides. Green Chemistry, 19(16), 3769–3779. https://doi.org/10.1039/c7gc01114h bibtex: '@article{Steinbauer_Spannenberg_Werner_2017, title={An in situ formed Ca²⁺–crown ether complex and its use in CO₂-fixation reactions with terminal and internal epoxides}, volume={19}, DOI={10.1039/c7gc01114h}, 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. Spannenberg, and Thomas Werner. “An in Situ Formed Ca²⁺–Crown Ether Complex and Its Use in CO₂-Fixation Reactions with Terminal and Internal Epoxides.” Green Chemistry 19, no. 16 (2017): 3769–79. https://doi.org/10.1039/c7gc01114h.' ieee: 'J. Steinbauer, A. Spannenberg, and T. Werner, “An in situ formed Ca²⁺–crown ether complex and its use in CO₂-fixation reactions with terminal and internal epoxides,” Green Chemistry, vol. 19, no. 16, pp. 3769–3779, 2017, doi: 10.1039/c7gc01114h.' mla: Steinbauer, J., et al. “An in Situ Formed Ca²⁺–Crown Ether Complex and Its Use in CO₂-Fixation Reactions with Terminal and Internal Epoxides.” Green Chemistry, vol. 19, no. 16, Royal Society of Chemistry (RSC), 2017, pp. 3769–79, doi:10.1039/c7gc01114h. short: J. Steinbauer, A. Spannenberg, T. Werner, Green Chemistry 19 (2017) 3769–3779. date_created: 2023-01-22T20:59:12Z date_updated: 2025-11-10T09:18:18Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1039/c7gc01114h extern: '1' intvolume: ' 19' issue: '16' keyword: - T1 - T3 - CSSD language: - iso: eng page: 3769-3779 publication: Green Chemistry publication_identifier: issn: - 1463-9262 - 1463-9270 publication_status: published publisher: Royal Society of Chemistry (RSC) status: public title: An in situ formed Ca²⁺–crown ether complex and its use in CO₂-fixation reactions with terminal and internal epoxides type: journal_article user_id: '89271' volume: 19 year: '2017' ... --- _id: '37977' article_number: '50' author: - first_name: Hendrik full_name: Büttner, Hendrik last_name: Büttner - first_name: Lars full_name: Longwitz, Lars last_name: Longwitz - first_name: Johannes full_name: Steinbauer, Johannes last_name: Steinbauer - first_name: Christoph full_name: Wulf, Christoph last_name: Wulf - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: 0000-0001-9025-3244 citation: ama: Büttner H, Longwitz L, Steinbauer J, Wulf C, Werner T. Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2. Topics in Current Chemistry. 2017;375(3). doi:10.1007/s41061-017-0136-5 apa: Büttner, H., Longwitz, L., Steinbauer, J., Wulf, C., & Werner, T. (2017). Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2. Topics in Current Chemistry, 375(3), Article 50. https://doi.org/10.1007/s41061-017-0136-5 bibtex: '@article{Büttner_Longwitz_Steinbauer_Wulf_Werner_2017, title={Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2}, volume={375}, DOI={10.1007/s41061-017-0136-5}, number={350}, journal={Topics in Current Chemistry}, publisher={Springer Science and Business Media LLC}, author={Büttner, Hendrik and Longwitz, Lars and Steinbauer, Johannes and Wulf, Christoph and Werner, Thomas}, year={2017} }' chicago: Büttner, Hendrik, Lars Longwitz, Johannes Steinbauer, Christoph Wulf, and Thomas Werner. “Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2.” Topics in Current Chemistry 375, no. 3 (2017). https://doi.org/10.1007/s41061-017-0136-5. ieee: 'H. Büttner, L. Longwitz, J. Steinbauer, C. Wulf, and T. Werner, “Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2,” Topics in Current Chemistry, vol. 375, no. 3, Art. no. 50, 2017, doi: 10.1007/s41061-017-0136-5.' mla: Büttner, Hendrik, et al. “Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2.” Topics in Current Chemistry, vol. 375, no. 3, 50, Springer Science and Business Media LLC, 2017, doi:10.1007/s41061-017-0136-5. short: H. Büttner, L. Longwitz, J. Steinbauer, C. Wulf, T. Werner, Topics in Current Chemistry 375 (2017). date_created: 2023-01-22T20:59:56Z date_updated: 2025-11-10T09:17:38Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1007/s41061-017-0136-5 extern: '1' intvolume: ' 375' issue: '3' keyword: - T1 - CSSD language: - iso: eng publication: Topics in Current Chemistry publication_identifier: issn: - 2365-0869 - 2364-8961 publication_status: published publisher: Springer Science and Business Media LLC status: public title: Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2 type: journal_article user_id: '89271' volume: 375 year: '2017' ... --- _id: '37972' author: - first_name: Wu full_name: Li, Wu last_name: Li - first_name: Ming-Ming full_name: Wang, Ming-Ming last_name: Wang - first_name: Yuya full_name: Hu, Yuya last_name: Hu - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: 0000-0001-9025-3244 citation: ama: Li W, Wang M-M, Hu Y, Werner T. B(C₆F₅)₃-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds. Organic Letters. 2017;19(21):5768-5771. doi:10.1021/acs.orglett.7b02701 apa: Li, W., Wang, M.-M., Hu, Y., & Werner, T. (2017). B(C₆F₅)₃-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds. Organic Letters, 19(21), 5768–5771. https://doi.org/10.1021/acs.orglett.7b02701 bibtex: '@article{Li_Wang_Hu_Werner_2017, title={B(C₆F₅)₃-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds}, volume={19}, DOI={10.1021/acs.orglett.7b02701}, number={21}, journal={Organic Letters}, publisher={American Chemical Society (ACS)}, author={Li, Wu and Wang, Ming-Ming and Hu, Yuya and Werner, Thomas}, year={2017}, pages={5768–5771} }' chicago: 'Li, Wu, Ming-Ming Wang, Yuya Hu, and Thomas Werner. “B(C₆F₅)₃-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds.” Organic Letters 19, no. 21 (2017): 5768–71. https://doi.org/10.1021/acs.orglett.7b02701.' ieee: 'W. Li, M.-M. Wang, Y. Hu, and T. Werner, “B(C₆F₅)₃-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds,” Organic Letters, vol. 19, no. 21, pp. 5768–5771, 2017, doi: 10.1021/acs.orglett.7b02701.' mla: Li, Wu, et al. “B(C₆F₅)₃-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds.” Organic Letters, vol. 19, no. 21, American Chemical Society (ACS), 2017, pp. 5768–71, doi:10.1021/acs.orglett.7b02701. short: W. Li, M.-M. Wang, Y. Hu, T. Werner, Organic Letters 19 (2017) 5768–5771. date_created: 2023-01-22T20:57:15Z date_updated: 2025-11-10T09:18:33Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1021/acs.orglett.7b02701 extern: '1' intvolume: ' 19' issue: '21' keyword: - CSSD language: - iso: eng page: 5768-5771 publication: Organic Letters publication_identifier: issn: - 1523-7060 - 1523-7052 publication_status: published publisher: American Chemical Society (ACS) status: public title: B(C₆F₅)₃-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds type: journal_article user_id: '89271' volume: 19 year: '2017' ... --- _id: '37978' author: - first_name: Hendrik full_name: Büttner, Hendrik last_name: Büttner - first_name: Johannes full_name: Steinbauer, Johannes last_name: Steinbauer - first_name: Christoph full_name: Wulf, Christoph last_name: Wulf - first_name: Mehmet full_name: Dindaroglu, Mehmet last_name: Dindaroglu - first_name: Hans-Günther full_name: Schmalz, Hans-Günther last_name: Schmalz - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: 0000-0001-9025-3244 citation: ama: Büttner H, Steinbauer J, Wulf C, Dindaroglu M, Schmalz H-G, Werner T. Organocatalyzed Synthesis of Oleochemical Carbonates from CO₂and Renewables. ChemSusChem. 2017;10(6):1076-1079. doi:10.1002/cssc.201601163 apa: Büttner, H., Steinbauer, J., Wulf, C., Dindaroglu, M., Schmalz, H.-G., & Werner, T. (2017). Organocatalyzed Synthesis of Oleochemical Carbonates from CO₂and Renewables. ChemSusChem, 10(6), 1076–1079. https://doi.org/10.1002/cssc.201601163 bibtex: '@article{Büttner_Steinbauer_Wulf_Dindaroglu_Schmalz_Werner_2017, title={Organocatalyzed Synthesis of Oleochemical Carbonates from CO₂and Renewables}, volume={10}, DOI={10.1002/cssc.201601163}, 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} }' chicago: 'Büttner, Hendrik, Johannes Steinbauer, Christoph Wulf, Mehmet Dindaroglu, Hans-Günther Schmalz, and Thomas Werner. “Organocatalyzed Synthesis of Oleochemical Carbonates from CO₂and Renewables.” ChemSusChem 10, no. 6 (2017): 1076–79. https://doi.org/10.1002/cssc.201601163.' ieee: 'H. Büttner, J. Steinbauer, C. Wulf, M. Dindaroglu, H.-G. Schmalz, and T. Werner, “Organocatalyzed Synthesis of Oleochemical Carbonates from CO₂and Renewables,” ChemSusChem, vol. 10, no. 6, pp. 1076–1079, 2017, doi: 10.1002/cssc.201601163.' mla: Büttner, Hendrik, et al. “Organocatalyzed Synthesis of Oleochemical Carbonates from CO₂and Renewables.” ChemSusChem, vol. 10, no. 6, Wiley, 2017, pp. 1076–79, doi:10.1002/cssc.201601163. short: H. Büttner, J. Steinbauer, C. Wulf, M. Dindaroglu, H.-G. Schmalz, T. Werner, ChemSusChem 10 (2017) 1076–1079. date_created: 2023-01-22T21:00:17Z date_updated: 2025-11-10T09:17:59Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1002/cssc.201601163 extern: '1' intvolume: ' 10' issue: '6' keyword: - T1 - T2 - CSSD language: - iso: eng page: 1076-1079 publication: ChemSusChem publication_identifier: issn: - 1864-5631 publication_status: published publisher: Wiley status: public title: Organocatalyzed Synthesis of Oleochemical Carbonates from CO₂and Renewables type: journal_article user_id: '89271' volume: 10 year: '2017' ... --- _id: '37974' author: - first_name: Johannes full_name: Steinbauer, Johannes last_name: Steinbauer - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: 0000-0001-9025-3244 citation: ama: Steinbauer J, Werner T. Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis. ChemSusChem. 2017;10(15):3025-3029. doi:10.1002/cssc.201700788 apa: Steinbauer, J., & Werner, T. (2017). Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis. ChemSusChem, 10(15), 3025–3029. https://doi.org/10.1002/cssc.201700788 bibtex: '@article{Steinbauer_Werner_2017, title={Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis}, volume={10}, DOI={10.1002/cssc.201700788}, number={15}, journal={ChemSusChem}, publisher={Wiley}, author={Steinbauer, Johannes and Werner, Thomas}, year={2017}, pages={3025–3029} }' chicago: 'Steinbauer, Johannes, and Thomas Werner. “Poly(Ethylene Glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis.” ChemSusChem 10, no. 15 (2017): 3025–29. https://doi.org/10.1002/cssc.201700788.' ieee: 'J. Steinbauer and T. Werner, “Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis,” ChemSusChem, vol. 10, no. 15, pp. 3025–3029, 2017, doi: 10.1002/cssc.201700788.' mla: Steinbauer, Johannes, and Thomas Werner. “Poly(Ethylene Glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis.” ChemSusChem, vol. 10, no. 15, Wiley, 2017, pp. 3025–29, doi:10.1002/cssc.201700788. short: J. Steinbauer, T. Werner, ChemSusChem 10 (2017) 3025–3029. date_created: 2023-01-22T20:58:02Z date_updated: 2025-11-10T09:17:48Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1002/cssc.201700788 extern: '1' intvolume: ' 10' issue: '15' keyword: - T1 - T3 - CSSD language: - iso: eng page: 3025-3029 publication: ChemSusChem publication_identifier: issn: - 1864-5631 publication_status: published publisher: Wiley status: public title: Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis type: journal_article user_id: '89271' volume: 10 year: '2017' ... --- _id: '13412' author: - first_name: Dagny D. full_name: Konieczna, Dagny D. last_name: Konieczna - first_name: Harry full_name: Biller, Harry last_name: Biller - first_name: Matthias full_name: Witte, Matthias last_name: Witte - first_name: Wolf Gero full_name: Schmidt, Wolf Gero id: '468' last_name: Schmidt orcid: 0000-0002-2717-5076 - first_name: Adam full_name: Neuba, Adam last_name: Neuba - first_name: René full_name: Wilhelm, René last_name: Wilhelm citation: ama: Konieczna DD, Biller H, Witte M, Schmidt WG, Neuba A, Wilhelm R. New pyridinium based ionic dyes for the hydrogen evolution reaction. Tetrahedron. Published online 2017:142-149. doi:10.1016/j.tet.2017.11.053 apa: Konieczna, D. D., Biller, H., Witte, M., Schmidt, W. G., Neuba, A., & Wilhelm, R. (2017). New pyridinium based ionic dyes for the hydrogen evolution reaction. Tetrahedron, 142–149. https://doi.org/10.1016/j.tet.2017.11.053 bibtex: '@article{Konieczna_Biller_Witte_Schmidt_Neuba_Wilhelm_2017, title={New pyridinium based ionic dyes for the hydrogen evolution reaction}, DOI={10.1016/j.tet.2017.11.053}, journal={Tetrahedron}, author={Konieczna, Dagny D. and Biller, Harry and Witte, Matthias and Schmidt, Wolf Gero and Neuba, Adam and Wilhelm, René}, year={2017}, pages={142–149} }' chicago: Konieczna, Dagny D., Harry Biller, Matthias Witte, Wolf Gero Schmidt, Adam Neuba, and René Wilhelm. “New Pyridinium Based Ionic Dyes for the Hydrogen Evolution Reaction.” Tetrahedron, 2017, 142–49. https://doi.org/10.1016/j.tet.2017.11.053. ieee: 'D. D. Konieczna, H. Biller, M. Witte, W. G. Schmidt, A. Neuba, and R. Wilhelm, “New pyridinium based ionic dyes for the hydrogen evolution reaction,” Tetrahedron, pp. 142–149, 2017, doi: 10.1016/j.tet.2017.11.053.' mla: Konieczna, Dagny D., et al. “New Pyridinium Based Ionic Dyes for the Hydrogen Evolution Reaction.” Tetrahedron, 2017, pp. 142–49, doi:10.1016/j.tet.2017.11.053. short: D.D. Konieczna, H. Biller, M. Witte, W.G. Schmidt, A. Neuba, R. Wilhelm, Tetrahedron (2017) 142–149. date_created: 2019-09-20T11:33:20Z date_updated: 2025-12-05T10:16:13Z department: - _id: '15' - _id: '170' - _id: '295' - _id: '2' - _id: '312' - _id: '35' - _id: '230' - _id: '27' doi: 10.1016/j.tet.2017.11.053 language: - iso: eng page: 142-149 project: - _id: '52' name: Computing Resources Provided by the Paderborn Center for Parallel Computing publication: Tetrahedron publication_identifier: issn: - 0040-4020 publication_status: published status: public title: New pyridinium based ionic dyes for the hydrogen evolution reaction type: journal_article user_id: '16199' year: '2017' ... --- _id: '64888' abstract: - lang: eng text: AbstractManche boranbasierten frustrierten Lewis‐Paare spalten Wasserstoff – wie, war bislang unklar. Um Struktur und Reaktivität in Beziehung zu setzen, werden quantenchemische Untersuchungen und NMR‐Experimente kombiniert. Sind pKa‐Werte der Lewis‐Base bekannt, lässt sich damit Reaktivität vorhersagen. author: - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X citation: ama: Paradies J. Reaktivität verstehen, ohne die Katalysatorstruktur zu kennen. Nachrichten aus der Chemie. 2017;65(2):118-122. doi:10.1002/nadc.20174055283 apa: Paradies, J. (2017). Reaktivität verstehen, ohne die Katalysatorstruktur zu kennen. Nachrichten Aus Der Chemie, 65(2), 118–122. https://doi.org/10.1002/nadc.20174055283 bibtex: '@article{Paradies_2017, title={Reaktivität verstehen, ohne die Katalysatorstruktur zu kennen}, volume={65}, DOI={10.1002/nadc.20174055283}, number={2}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Paradies, Jan}, year={2017}, pages={118–122} }' chicago: 'Paradies, Jan. “Reaktivität Verstehen, Ohne Die Katalysatorstruktur Zu Kennen.” Nachrichten Aus Der Chemie 65, no. 2 (2017): 118–22. https://doi.org/10.1002/nadc.20174055283.' ieee: 'J. Paradies, “Reaktivität verstehen, ohne die Katalysatorstruktur zu kennen,” Nachrichten aus der Chemie, vol. 65, no. 2, pp. 118–122, 2017, doi: 10.1002/nadc.20174055283.' mla: Paradies, Jan. “Reaktivität Verstehen, Ohne Die Katalysatorstruktur Zu Kennen.” Nachrichten Aus Der Chemie, vol. 65, no. 2, Wiley, 2017, pp. 118–22, doi:10.1002/nadc.20174055283. short: J. Paradies, Nachrichten Aus Der Chemie 65 (2017) 118–122. date_created: 2026-03-11T10:15:53Z date_updated: 2026-03-11T10:15:59Z department: - _id: '2' - _id: '389' doi: 10.1002/nadc.20174055283 intvolume: ' 65' issue: '2' language: - iso: eng page: 118-122 publication: Nachrichten aus der Chemie publication_identifier: issn: - 1439-9598 - 1868-0054 publication_status: published publisher: Wiley status: public title: Reaktivität verstehen, ohne die Katalysatorstruktur zu kennen type: journal_article user_id: '53339' volume: 65 year: '2017' ... --- _id: '64899' author: - first_name: Bernd F. full_name: Straub, Bernd F. last_name: Straub - first_name: Jennifer full_name: Andexer, Jennifer last_name: Andexer - first_name: Christoph full_name: Arenz, Christoph last_name: Arenz - first_name: Uwe full_name: Beifuss, Uwe last_name: Beifuss - first_name: Florian full_name: Beuerle, Florian last_name: Beuerle - first_name: Malte full_name: Brasholz, Malte last_name: Brasholz - first_name: Rolf full_name: Breinbauer, Rolf last_name: Breinbauer - first_name: Klaus full_name: Ditrich, Klaus last_name: Ditrich - first_name: Tobias A. M. full_name: Gulder, Tobias A. M. last_name: Gulder - first_name: Wolfgang full_name: Hüttel, Wolfgang last_name: Hüttel - first_name: Markus full_name: Kordes, Markus last_name: Kordes - first_name: Anke full_name: Krueger, Anke last_name: Krueger - first_name: Matthias full_name: Lehmann, Matthias last_name: Lehmann - first_name: Thomas full_name: Lindel, Thomas last_name: Lindel - first_name: Burkhard full_name: Luy, Burkhard last_name: Luy - first_name: Michael A. R. full_name: Meier, Michael A. R. last_name: Meier - first_name: Christian full_name: Mück-Lichtenfeld, Christian last_name: Mück-Lichtenfeld - first_name: Claudia full_name: Muhle-Goll, Claudia last_name: Muhle-Goll - first_name: Thomas J. J. full_name: Müller, Thomas J. J. last_name: Müller - first_name: Arun full_name: Narine, Arun last_name: Narine - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X - first_name: Roland full_name: Pfau, Roland last_name: Pfau - first_name: Jörg full_name: Pietruszka, Jörg last_name: Pietruszka - first_name: Norbert full_name: Schaschke, Norbert last_name: Schaschke - first_name: Mathias O. full_name: Senge, Mathias O. last_name: Senge - first_name: Thomas full_name: Werner, Thomas last_name: Werner - first_name: Daniel B. full_name: Werz, Daniel B. last_name: Werz - first_name: Christian A. full_name: Winter, Christian A. last_name: Winter - first_name: Dennis full_name: Worgull, Dennis last_name: Worgull citation: ama: Straub BF, Andexer J, Arenz C, et al. Organische Chemie 2016. Nachrichten aus der Chemie. 2017;65(3):266-304. doi:10.1002/nadc.20174059831 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. Nachrichten Aus Der Chemie, 65(3), 266–304. https://doi.org/10.1002/nadc.20174059831 bibtex: '@article{Straub_Andexer_Arenz_Beifuss_Beuerle_Brasholz_Breinbauer_Ditrich_Gulder_Hüttel_et al._2017, title={Organische Chemie 2016}, volume={65}, DOI={10.1002/nadc.20174059831}, 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} }' chicago: 'Straub, Bernd F., Jennifer Andexer, Christoph Arenz, Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, et al. “Organische Chemie 2016.” Nachrichten Aus Der Chemie 65, no. 3 (2017): 266–304. https://doi.org/10.1002/nadc.20174059831.' ieee: 'B. F. Straub et al., “Organische Chemie 2016,” Nachrichten aus der Chemie, vol. 65, no. 3, pp. 266–304, 2017, doi: 10.1002/nadc.20174059831.' mla: Straub, Bernd F., et al. “Organische Chemie 2016.” Nachrichten Aus Der Chemie, vol. 65, no. 3, Wiley, 2017, pp. 266–304, doi:10.1002/nadc.20174059831. 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. date_created: 2026-03-11T10:25:45Z date_updated: 2026-03-11T10:26:39Z department: - _id: '2' - _id: '389' doi: 10.1002/nadc.20174059831 intvolume: ' 65' issue: '3' language: - iso: eng page: 266-304 publication: Nachrichten aus der Chemie publication_identifier: issn: - 1439-9598 publication_status: published publisher: Wiley status: public title: Organische Chemie 2016 type: journal_article user_id: '53339' volume: 65 year: '2017' ... --- _id: '64900' author: - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X citation: ama: 'Paradies J. Chiral Borane-Based Lewis Acids for Metal Free Hydrogenations. In: Topics in Organometallic Chemistry. Springer International Publishing; 2017. doi:10.1007/3418_2016_173' apa: Paradies, J. (2017). Chiral Borane-Based Lewis Acids for Metal Free Hydrogenations. In Topics in Organometallic Chemistry. Springer International Publishing. https://doi.org/10.1007/3418_2016_173 bibtex: '@inbook{Paradies_2017, place={Cham}, title={Chiral Borane-Based Lewis Acids for Metal Free Hydrogenations}, DOI={10.1007/3418_2016_173}, booktitle={Topics in Organometallic Chemistry}, publisher={Springer International Publishing}, author={Paradies, Jan}, year={2017} }' chicago: 'Paradies, Jan. “Chiral Borane-Based Lewis Acids for Metal Free Hydrogenations.” In Topics in Organometallic Chemistry. Cham: Springer International Publishing, 2017. https://doi.org/10.1007/3418_2016_173.' ieee: 'J. Paradies, “Chiral Borane-Based Lewis Acids for Metal Free Hydrogenations,” in Topics in Organometallic Chemistry, Cham: Springer International Publishing, 2017.' mla: Paradies, Jan. “Chiral Borane-Based Lewis Acids for Metal Free Hydrogenations.” Topics in Organometallic Chemistry, Springer International Publishing, 2017, doi:10.1007/3418_2016_173. short: 'J. Paradies, in: Topics in Organometallic Chemistry, Springer International Publishing, Cham, 2017.' date_created: 2026-03-11T10:30:16Z date_updated: 2026-03-11T10:34:43Z department: - _id: '2' - _id: '389' doi: 10.1007/3418_2016_173 language: - iso: eng place: Cham publication: Topics in Organometallic Chemistry publication_identifier: isbn: - '9783319708041' - '9783319708065' issn: - 1436-6002 - 1616-8534 publication_status: published publisher: Springer International Publishing status: public title: Chiral Borane-Based Lewis Acids for Metal Free Hydrogenations type: book_chapter user_id: '53339' year: '2017' ... --- _id: '35706' author: - first_name: Peter full_name: Oechsle, Peter last_name: Oechsle - first_name: Peng full_name: Hou, Peng last_name: Hou - first_name: Ulrich full_name: Flörke, Ulrich last_name: Flörke - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X citation: ama: Oechsle P, Hou P, Flörke U, Paradies J. Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence. Advanced Synthesis & Catalysis. 2016;358(23):3770-3776. doi:10.1002/adsc.201600802 apa: Oechsle, P., Hou, P., Flörke, U., & Paradies, J. (2016). Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence. Advanced Synthesis & Catalysis, 358(23), 3770–3776. https://doi.org/10.1002/adsc.201600802 bibtex: '@article{Oechsle_Hou_Flörke_Paradies_2016, title={Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence}, volume={358}, DOI={10.1002/adsc.201600802}, number={23}, journal={Advanced Synthesis & Catalysis}, publisher={Wiley}, author={Oechsle, Peter and Hou, Peng and Flörke, Ulrich and Paradies, Jan}, year={2016}, pages={3770–3776} }' chicago: 'Oechsle, Peter, Peng Hou, Ulrich Flörke, and Jan Paradies. “Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence.” Advanced Synthesis & Catalysis 358, no. 23 (2016): 3770–76. https://doi.org/10.1002/adsc.201600802.' ieee: 'P. Oechsle, P. Hou, U. Flörke, and J. Paradies, “Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence,” Advanced Synthesis & Catalysis, vol. 358, no. 23, pp. 3770–3776, 2016, doi: 10.1002/adsc.201600802.' mla: Oechsle, Peter, et al. “Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence.” Advanced Synthesis & Catalysis, vol. 358, no. 23, Wiley, 2016, pp. 3770–76, doi:10.1002/adsc.201600802. short: P. Oechsle, P. Hou, U. Flörke, J. Paradies, Advanced Synthesis & Catalysis 358 (2016) 3770–3776. date_created: 2023-01-10T09:12:45Z date_updated: 2024-07-24T09:15:18Z department: - _id: '2' - _id: '389' doi: 10.1002/adsc.201600802 intvolume: ' 358' issue: '23' keyword: - General Chemistry language: - iso: eng page: 3770-3776 publication: Advanced Synthesis & Catalysis publication_identifier: issn: - 1615-4150 publication_status: published publisher: Wiley status: public title: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence type: journal_article user_id: '53339' volume: 358 year: '2016' ... --- _id: '35708' author: - first_name: Peter full_name: Oechsle, Peter last_name: Oechsle - first_name: Peng full_name: Hou, Peng last_name: Hou - first_name: Ulrich full_name: Flörke, Ulrich last_name: Flörke - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X citation: ama: 'Oechsle P, Hou P, Flörke U, Paradies J. Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016). Advanced Synthesis & Catalysis. 2016;358(23):3656-3656. doi:10.1002/adsc.201601149' apa: 'Oechsle, P., Hou, P., Flörke, U., & Paradies, J. (2016). Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016). Advanced Synthesis & Catalysis, 358(23), 3656–3656. https://doi.org/10.1002/adsc.201601149' bibtex: '@article{Oechsle_Hou_Flörke_Paradies_2016, title={Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016)}, volume={358}, DOI={10.1002/adsc.201601149}, number={23}, journal={Advanced Synthesis & Catalysis}, publisher={Wiley}, author={Oechsle, Peter and Hou, Peng and Flörke, Ulrich and Paradies, Jan}, year={2016}, pages={3656–3656} }' chicago: 'Oechsle, Peter, Peng Hou, Ulrich Flörke, and Jan Paradies. “Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016).” Advanced Synthesis & Catalysis 358, no. 23 (2016): 3656–3656. https://doi.org/10.1002/adsc.201601149.' ieee: 'P. Oechsle, P. Hou, U. Flörke, and J. Paradies, “Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016),” Advanced Synthesis & Catalysis, vol. 358, no. 23, pp. 3656–3656, 2016, doi: 10.1002/adsc.201601149.' mla: 'Oechsle, Peter, et al. “Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016).” Advanced Synthesis & Catalysis, vol. 358, no. 23, Wiley, 2016, pp. 3656–3656, doi:10.1002/adsc.201601149.' short: P. Oechsle, P. Hou, U. Flörke, J. Paradies, Advanced Synthesis & Catalysis 358 (2016) 3656–3656. date_created: 2023-01-10T09:13:12Z date_updated: 2023-01-23T12:47:30Z department: - _id: '2' - _id: '389' doi: 10.1002/adsc.201601149 intvolume: ' 358' issue: '23' keyword: - General Chemistry language: - iso: eng page: 3656-3656 publication: Advanced Synthesis & Catalysis publication_identifier: issn: - 1615-4150 publication_status: published publisher: Wiley status: public title: 'Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016)' type: journal_article user_id: '53339' volume: 358 year: '2016' ... --- _id: '35710' author: - first_name: Sebastian full_name: Tussing, Sebastian last_name: Tussing - first_name: Karl full_name: Kaupmees, Karl last_name: Kaupmees - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X citation: ama: 'Tussing S, Kaupmees K, Paradies J. Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016). Chemistry – A European Journal. 2016;22(22):7302-7302. doi:10.1002/chem.201601558' apa: 'Tussing, S., Kaupmees, K., & Paradies, J. (2016). Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016). Chemistry – A European Journal, 22(22), 7302–7302. https://doi.org/10.1002/chem.201601558' bibtex: '@article{Tussing_Kaupmees_Paradies_2016, title={Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016)}, volume={22}, DOI={10.1002/chem.201601558}, number={22}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Tussing, Sebastian and Kaupmees, Karl and Paradies, Jan}, year={2016}, pages={7302–7302} }' chicago: 'Tussing, Sebastian, Karl Kaupmees, and Jan Paradies. “Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016).” Chemistry – A European Journal 22, no. 22 (2016): 7302–7302. https://doi.org/10.1002/chem.201601558.' ieee: 'S. Tussing, K. Kaupmees, and J. Paradies, “Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016),” Chemistry – A European Journal, vol. 22, no. 22, pp. 7302–7302, 2016, doi: 10.1002/chem.201601558.' mla: 'Tussing, Sebastian, et al. “Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016).” Chemistry – A European Journal, vol. 22, no. 22, Wiley, 2016, pp. 7302–7302, doi:10.1002/chem.201601558.' short: S. Tussing, K. Kaupmees, J. Paradies, Chemistry – A European Journal 22 (2016) 7302–7302. date_created: 2023-01-10T09:13:44Z date_updated: 2023-01-23T12:54:23Z department: - _id: '2' - _id: '389' doi: 10.1002/chem.201601558 intvolume: ' 22' issue: '22' keyword: - General Chemistry - Catalysis - Organic Chemistry language: - iso: eng page: 7302-7302 publication: Chemistry – A European Journal publication_identifier: issn: - 0947-6539 - 1521-3765 publication_status: published publisher: Wiley status: public title: 'Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016)' type: journal_article user_id: '53339' volume: 22 year: '2016' ... --- _id: '37983' abstract: - lang: eng text:

Taking Control!The binary catalyst system composed of MoO₃and an organic phoshponium salt [Bu₄P]X proved very efficient to produce oleochemical cyclic carbonates from renewables.

author: - first_name: Nils full_name: Tenhumberg, Nils last_name: Tenhumberg - first_name: Hendrik full_name: Büttner, Hendrik last_name: Büttner - first_name: Benjamin full_name: Schäffner, Benjamin last_name: Schäffner - first_name: Daniela full_name: Kruse, Daniela last_name: Kruse - first_name: Michael full_name: Blumenstein, Michael last_name: Blumenstein - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: 0000-0001-9025-3244 citation: ama: Tenhumberg N, Büttner H, Schäffner B, Kruse D, Blumenstein M, Werner T. Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO₂and renewables. Green Chemistry. 2016;18(13):3775-3788. doi:10.1039/c6gc00671j apa: Tenhumberg, N., Büttner, H., Schäffner, B., Kruse, D., Blumenstein, M., & Werner, T. (2016). Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO₂and renewables. Green Chemistry, 18(13), 3775–3788. https://doi.org/10.1039/c6gc00671j bibtex: '@article{Tenhumberg_Büttner_Schäffner_Kruse_Blumenstein_Werner_2016, title={Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO₂and renewables}, volume={18}, DOI={10.1039/c6gc00671j}, number={13}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Tenhumberg, Nils and Büttner, Hendrik and Schäffner, Benjamin and Kruse, Daniela and Blumenstein, Michael and Werner, Thomas}, year={2016}, pages={3775–3788} }' chicago: 'Tenhumberg, Nils, Hendrik Büttner, Benjamin Schäffner, Daniela Kruse, Michael Blumenstein, and Thomas Werner. “Cooperative Catalyst System for the Synthesis of Oleochemical Cyclic Carbonates from CO₂and Renewables.” Green Chemistry 18, no. 13 (2016): 3775–88. https://doi.org/10.1039/c6gc00671j.' ieee: 'N. Tenhumberg, H. Büttner, B. Schäffner, D. Kruse, M. Blumenstein, and T. Werner, “Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO₂and renewables,” Green Chemistry, vol. 18, no. 13, pp. 3775–3788, 2016, doi: 10.1039/c6gc00671j.' mla: Tenhumberg, Nils, et al. “Cooperative Catalyst System for the Synthesis of Oleochemical Cyclic Carbonates from CO₂and Renewables.” Green Chemistry, vol. 18, no. 13, Royal Society of Chemistry (RSC), 2016, pp. 3775–88, doi:10.1039/c6gc00671j. short: N. Tenhumberg, H. Büttner, B. Schäffner, D. Kruse, M. Blumenstein, T. Werner, Green Chemistry 18 (2016) 3775–3788. date_created: 2023-01-22T21:03:02Z date_updated: 2025-11-10T09:20:35Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1039/c6gc00671j extern: '1' intvolume: ' 18' issue: '13' keyword: - T1 - T3 - CSSD language: - iso: eng page: 3775-3788 publication: Green Chemistry publication_identifier: issn: - 1463-9262 - 1463-9270 publication_status: published publisher: Royal Society of Chemistry (RSC) status: public title: Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO₂and renewables type: journal_article user_id: '89271' volume: 18 year: '2016' ... --- _id: '37989' author: - first_name: Marie-Luis full_name: Schirmer, Marie-Luis last_name: Schirmer - first_name: Stefan full_name: Jopp, Stefan last_name: Jopp - first_name: Jens full_name: Holz, Jens last_name: Holz - first_name: Anke full_name: Spannenberg, Anke last_name: Spannenberg - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: 0000-0001-9025-3244 citation: ama: Schirmer M-L, Jopp S, Holz J, Spannenberg A, Werner T. Organocatalyzed Reduction of Tertiary Phosphine Oxides. Advanced Synthesis and Catalysis. 2016;358(1):26-29. doi:10.1002/adsc.201500762 apa: Schirmer, M.-L., Jopp, S., Holz, J., Spannenberg, A., & Werner, T. (2016). Organocatalyzed Reduction of Tertiary Phosphine Oxides. Advanced Synthesis and Catalysis, 358(1), 26–29. https://doi.org/10.1002/adsc.201500762 bibtex: '@article{Schirmer_Jopp_Holz_Spannenberg_Werner_2016, title={Organocatalyzed Reduction of Tertiary Phosphine Oxides}, volume={358}, DOI={10.1002/adsc.201500762}, number={1}, journal={Advanced Synthesis and Catalysis}, publisher={Wiley}, author={Schirmer, Marie-Luis and Jopp, Stefan and Holz, Jens and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={26–29} }' chicago: 'Schirmer, Marie-Luis, Stefan Jopp, Jens Holz, Anke Spannenberg, and Thomas Werner. “Organocatalyzed Reduction of Tertiary Phosphine Oxides.” Advanced Synthesis and Catalysis 358, no. 1 (2016): 26–29. https://doi.org/10.1002/adsc.201500762.' ieee: 'M.-L. Schirmer, S. Jopp, J. Holz, A. Spannenberg, and T. Werner, “Organocatalyzed Reduction of Tertiary Phosphine Oxides,” Advanced Synthesis and Catalysis, vol. 358, no. 1, pp. 26–29, 2016, doi: 10.1002/adsc.201500762.' mla: Schirmer, Marie-Luis, et al. “Organocatalyzed Reduction of Tertiary Phosphine Oxides.” Advanced Synthesis and Catalysis, vol. 358, no. 1, Wiley, 2016, pp. 26–29, doi:10.1002/adsc.201500762. short: M.-L. Schirmer, S. Jopp, J. Holz, A. Spannenberg, T. Werner, Advanced Synthesis and Catalysis 358 (2016) 26–29. date_created: 2023-01-22T21:05:14Z date_updated: 2025-11-10T09:22:07Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1002/adsc.201500762 extern: '1' intvolume: ' 358' issue: '1' keyword: - T2 - CSSD language: - iso: eng page: 26-29 publication: Advanced Synthesis and Catalysis publication_identifier: issn: - 1615-4150 publication_status: published publisher: Wiley status: public title: Organocatalyzed Reduction of Tertiary Phosphine Oxides type: journal_article user_id: '89271' volume: 358 year: '2016' ... --- _id: '37984' abstract: - lang: eng text: The Wittig reaction is a fundamental transformation for the preparation of alkenes from carbonyl compounds and phosphonium ylides. The ylides are prepared prior to the olefination step from the respective phosphonium salts by deprotonation utilizing strong bases. A first free-base catalytic Wittig reaction for the preparation of highly functionalized alkenes was based on tributylphosphane as the catalyst. Subsequently we developed a system employing a phospholene oxide as a pre-catalyst and trimethoxysilane as reducing agent which operates under milder conditions. The title compounds, (E)-3-benzylidenepyrrolidine-2,5-dione, C11H9NO2, (I), the methylpyrrolidine derivative, C12H11NO2, (II), and thetert-butylpyrrolidine derivative, C15H17NO2, (III), have been synthesized by base-free catalytic Wittig reactions. In the crystal of (I), molecules are linked into centrosymmetric dimersviapairs of N—H...O hydrogen bonds. Furthermore, in the crystal structure of (III), there are two molecules in the asymmetric unit, whereas in (I) and (II), only one molecule is present. author: - first_name: Marie-Luis full_name: Schirmer, Marie-Luis last_name: Schirmer - first_name: Anke full_name: Spannenberg, Anke last_name: Spannenberg - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: 0000-0001-9025-3244 citation: ama: 'Schirmer M-L, Spannenberg A, Werner T. Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (E)-3-benzylidenepyrrolidine-2,5-dione, (E)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (E)-3-benzylidene-1-tert-butylpyrrolidine-2,5-dione. Acta Crystallographica Section C Structural Chemistry. 2016;72(6):504-508. doi:10.1107/s2053229616008159' apa: 'Schirmer, M.-L., Spannenberg, A., & Werner, T. (2016). Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (E)-3-benzylidenepyrrolidine-2,5-dione, (E)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (E)-3-benzylidene-1-tert-butylpyrrolidine-2,5-dione. Acta Crystallographica Section C Structural Chemistry, 72(6), 504–508. https://doi.org/10.1107/s2053229616008159' bibtex: '@article{Schirmer_Spannenberg_Werner_2016, title={Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (E)-3-benzylidenepyrrolidine-2,5-dione, (E)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (E)-3-benzylidene-1-tert-butylpyrrolidine-2,5-dione}, volume={72}, DOI={10.1107/s2053229616008159}, number={6}, journal={Acta Crystallographica Section C Structural Chemistry}, publisher={International Union of Crystallography (IUCr)}, author={Schirmer, Marie-Luis and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={504–508} }' chicago: 'Schirmer, Marie-Luis, Anke Spannenberg, and Thomas Werner. “Highly Functionalized Alkenes Produced from Base-Free Organocatalytic Wittig Reactions: (E)-3-Benzylidenepyrrolidine-2,5-Dione, (E)-3-Benzylidene-1-Methylpyrrolidine-2,5-Dione and (E)-3-Benzylidene-1-Tert-Butylpyrrolidine-2,5-Dione.” Acta Crystallographica Section C Structural Chemistry 72, no. 6 (2016): 504–8. https://doi.org/10.1107/s2053229616008159.' ieee: 'M.-L. Schirmer, A. Spannenberg, and T. Werner, “Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (E)-3-benzylidenepyrrolidine-2,5-dione, (E)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (E)-3-benzylidene-1-tert-butylpyrrolidine-2,5-dione,” Acta Crystallographica Section C Structural Chemistry, vol. 72, no. 6, pp. 504–508, 2016, doi: 10.1107/s2053229616008159.' mla: 'Schirmer, Marie-Luis, et al. “Highly Functionalized Alkenes Produced from Base-Free Organocatalytic Wittig Reactions: (E)-3-Benzylidenepyrrolidine-2,5-Dione, (E)-3-Benzylidene-1-Methylpyrrolidine-2,5-Dione and (E)-3-Benzylidene-1-Tert-Butylpyrrolidine-2,5-Dione.” Acta Crystallographica Section C Structural Chemistry, vol. 72, no. 6, International Union of Crystallography (IUCr), 2016, pp. 504–08, doi:10.1107/s2053229616008159.' short: M.-L. Schirmer, A. Spannenberg, T. Werner, Acta Crystallographica Section C Structural Chemistry 72 (2016) 504–508. date_created: 2023-01-22T21:03:23Z date_updated: 2025-11-10T09:23:46Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1107/s2053229616008159 extern: '1' intvolume: ' 72' issue: '6' keyword: - T2 language: - iso: eng page: 504-508 publication: Acta Crystallographica Section C Structural Chemistry publication_identifier: issn: - 2053-2296 publication_status: published publisher: International Union of Crystallography (IUCr) status: public title: 'Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (E)-3-benzylidenepyrrolidine-2,5-dione, (E)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (E)-3-benzylidene-1-tert-butylpyrrolidine-2,5-dione' type: journal_article user_id: '89271' volume: 72 year: '2016' ... --- _id: '37981' abstract: - lang: eng text:

The lithium tert-butoxide catalyzed addition of CS₂ to epoxides and thiiranes under mild conditions is reported. A mechanism has been proposed taking into account the regio- and stereochemical outcome of the reaction.

author: - first_name: J. full_name: Diebler, J. last_name: Diebler - first_name: A. full_name: Spannenberg, A. last_name: Spannenberg - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: 0000-0001-9025-3244 citation: ama: Diebler J, Spannenberg A, Werner T. Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes. Organic and Biomolecular Chemistry. 2016;14(31):7480-7489. doi:10.1039/c6ob01081d apa: Diebler, J., Spannenberg, A., & Werner, T. (2016). Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes. Organic and Biomolecular Chemistry, 14(31), 7480–7489. https://doi.org/10.1039/c6ob01081d bibtex: '@article{Diebler_Spannenberg_Werner_2016, title={Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes}, volume={14}, DOI={10.1039/c6ob01081d}, number={31}, journal={Organic and Biomolecular Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Diebler, J. and Spannenberg, A. and Werner, Thomas}, year={2016}, pages={7480–7489} }' chicago: 'Diebler, J., A. Spannenberg, and Thomas Werner. “Atom Economical Synthesis of Di- and Trithiocarbonates by the Lithium Tert-Butoxide Catalyzed Addition of Carbon Disulfide to Epoxides and Thiiranes.” Organic and Biomolecular Chemistry 14, no. 31 (2016): 7480–89. https://doi.org/10.1039/c6ob01081d.' ieee: 'J. Diebler, A. Spannenberg, and T. Werner, “Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes,” Organic and Biomolecular Chemistry, vol. 14, no. 31, pp. 7480–7489, 2016, doi: 10.1039/c6ob01081d.' mla: Diebler, J., et al. “Atom Economical Synthesis of Di- and Trithiocarbonates by the Lithium Tert-Butoxide Catalyzed Addition of Carbon Disulfide to Epoxides and Thiiranes.” Organic and Biomolecular Chemistry, vol. 14, no. 31, Royal Society of Chemistry (RSC), 2016, pp. 7480–89, doi:10.1039/c6ob01081d. short: J. Diebler, A. Spannenberg, T. Werner, Organic and Biomolecular Chemistry 14 (2016) 7480–7489. date_created: 2023-01-22T21:01:59Z date_updated: 2025-11-10T09:24:16Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1039/c6ob01081d extern: '1' intvolume: ' 14' issue: '31' keyword: - CSSD language: - iso: eng page: 7480-7489 publication: Organic and Biomolecular Chemistry publication_identifier: issn: - 1477-0520 - 1477-0539 publication_status: published publisher: Royal Society of Chemistry (RSC) status: public title: Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes type: journal_article user_id: '89271' volume: 14 year: '2016' ...