[{"_id":"42879","date_updated":"2023-03-08T19:32:09Z","doi":"10.1002/ange.202301632","type":"journal_article","year":"2023","citation":{"apa":"Köring, L., Stepen, A., Birenheide, B., Barth, S., Leskov, M., Schoch, R., Krämer, F., Breher, F., & Paradies, J. (2023). Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation. Angewandte Chemie. https://doi.org/10.1002/ange.202301632","ama":"Köring L, Stepen A, Birenheide B, et al. Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation. Angewandte Chemie. Published online 2023. doi:10.1002/ange.202301632","chicago":"Köring, Laura, Arne Stepen, Bernhard Birenheide, Simon Barth, Maxim Leskov, Roland Schoch, Felix Krämer, Frank Breher, and Jan Paradies. “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation.” Angewandte Chemie, 2023. https://doi.org/10.1002/ange.202301632.","bibtex":"@article{Köring_Stepen_Birenheide_Barth_Leskov_Schoch_Krämer_Breher_Paradies_2023, title={Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation}, DOI={10.1002/ange.202301632}, journal={Angewandte Chemie}, publisher={Wiley}, author={Köring, Laura and Stepen, Arne and Birenheide, Bernhard and Barth, Simon and Leskov, Maxim and Schoch, Roland and Krämer, Felix and Breher, Frank and Paradies, Jan}, year={2023} }","mla":"Köring, Laura, et al. “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation.” Angewandte Chemie, Wiley, 2023, doi:10.1002/ange.202301632.","short":"L. Köring, A. Stepen, B. Birenheide, S. Barth, M. Leskov, R. Schoch, F. Krämer, F. Breher, J. Paradies, Angewandte Chemie (2023).","ieee":"L. Köring et al., “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation,” Angewandte Chemie, 2023, doi: 10.1002/ange.202301632."},"language":[{"iso":"eng"}],"title":"Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation","user_id":"53339","publisher":"Wiley","author":[{"full_name":"Köring, Laura","first_name":"Laura","last_name":"Köring"},{"last_name":"Stepen","first_name":"Arne","full_name":"Stepen, Arne"},{"first_name":"Bernhard","full_name":"Birenheide, Bernhard","last_name":"Birenheide"},{"full_name":"Barth, Simon","first_name":"Simon","last_name":"Barth"},{"last_name":"Leskov","full_name":"Leskov, Maxim","first_name":"Maxim"},{"last_name":"Schoch","first_name":"Roland","full_name":"Schoch, Roland"},{"full_name":"Krämer, Felix","first_name":"Felix","last_name":"Krämer"},{"full_name":"Breher, Frank","first_name":"Frank","last_name":"Breher"},{"full_name":"Paradies, Jan","orcid":"0000-0002-3698-668X","first_name":"Jan","id":"53339","last_name":"Paradies"}],"publication":"Angewandte Chemie","department":[{"_id":"2"},{"_id":"389"}],"keyword":["General Medicine"],"publication_status":"published","publication_identifier":{"issn":["0044-8249","1521-3757"]},"status":"public","date_created":"2023-03-08T19:31:03Z"},{"doi":"10.1002/anie.202217808","_id":"45571","date_updated":"2024-03-21T12:01:33Z","language":[{"iso":"eng"}],"year":"2023","type":"journal_article","citation":{"bibtex":"@article{Li_Kossmann_Zeng_Zhang_Wang_Weinberger_Antonietti_Odziomek_López‐Salas_2023, title={When High‐Temperature Cesium Chemistry Meets Self‐Templating: Metal Acetates as Building Blocks of Unusual Highly Porous Carbons}, DOI={10.1002/anie.202217808}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Li, Jiaxin and Kossmann, Janina and Zeng, Ke and Zhang, Kun and Wang, Bingjie and Weinberger, Christian and Antonietti, Markus and Odziomek, Mateusz and López‐Salas, Nieves}, year={2023} }","mla":"Li, Jiaxin, et al. “When High‐Temperature Cesium Chemistry Meets Self‐Templating: Metal Acetates as Building Blocks of Unusual Highly Porous Carbons.” Angewandte Chemie International Edition, Wiley, 2023, doi:10.1002/anie.202217808.","chicago":"Li, Jiaxin, Janina Kossmann, Ke Zeng, Kun Zhang, Bingjie Wang, Christian Weinberger, Markus Antonietti, Mateusz Odziomek, and Nieves López‐Salas. “When High‐Temperature Cesium Chemistry Meets Self‐Templating: Metal Acetates as Building Blocks of Unusual Highly Porous Carbons.” Angewandte Chemie International Edition, 2023. https://doi.org/10.1002/anie.202217808.","ama":"Li J, Kossmann J, Zeng K, et al. When High‐Temperature Cesium Chemistry Meets Self‐Templating: Metal Acetates as Building Blocks of Unusual Highly Porous Carbons. Angewandte Chemie International Edition. Published online 2023. doi:10.1002/anie.202217808","apa":"Li, J., Kossmann, J., Zeng, K., Zhang, K., Wang, B., Weinberger, C., Antonietti, M., Odziomek, M., & López‐Salas, N. (2023). When High‐Temperature Cesium Chemistry Meets Self‐Templating: Metal Acetates as Building Blocks of Unusual Highly Porous Carbons. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.202217808","ieee":"J. Li et al., “When High‐Temperature Cesium Chemistry Meets Self‐Templating: Metal Acetates as Building Blocks of Unusual Highly Porous Carbons,” Angewandte Chemie International Edition, 2023, doi: 10.1002/anie.202217808.","short":"J. Li, J. Kossmann, K. Zeng, K. Zhang, B. Wang, C. Weinberger, M. Antonietti, M. Odziomek, N. López‐Salas, Angewandte Chemie International Edition (2023)."},"user_id":"11848","title":"When High‐Temperature Cesium Chemistry Meets Self‐Templating: Metal Acetates as Building Blocks of Unusual Highly Porous Carbons","abstract":[{"text":"Self-templating is a facile strategy for synthesizing porous carbons by direct pyrolysis of organic metal salts. However, the method typically suffers from low yields (<4%) and limited specific surface areas (SSA<2000 m2 g−1) originating from low activity of metal cations (e.g., K+ or Na+) in promoting construction and activation of carbon frameworks. Here we use cesium acetate as the only precursor of oxo-carbons with large SSA of the order of 3000 m2 g−1, pore volume approaching 2 cm3 g−1, tunable oxygen contents, and yields of up to 15 %. We unravel the role of Cs+ as an efficient promoter of framework formation, templating and etching agent, while acetates act as carbon/oxygen sources of carbonaceous frameworks. The oxo-carbons show record-high CO2 uptake of 8.71 mmol g−1 and an ultimate specific capacitance of 313 F g−1 in the supercapacitor. This study helps to understand and rationally tailor the materials design by a still rare organic solid-state chemistry.","lang":"eng"}],"article_type":"original","date_created":"2023-06-12T07:42:09Z","status":"public","publication_identifier":{"issn":["0044-8249","1521-3757"]},"publication_status":"published","publication":"Angewandte Chemie International Edition","keyword":["CO2 Adsorption","Cesium Acetate","Cesium Effect","Porous Carbons","Supercapacitor"],"publisher":"Wiley","author":[{"last_name":"Li","first_name":"Jiaxin","full_name":"Li, Jiaxin"},{"first_name":"Janina","full_name":"Kossmann, Janina","last_name":"Kossmann"},{"last_name":"Zeng","full_name":"Zeng, Ke","first_name":"Ke"},{"last_name":"Zhang","full_name":"Zhang, Kun","first_name":"Kun"},{"last_name":"Wang","first_name":"Bingjie","full_name":"Wang, Bingjie"},{"id":"11848","last_name":"Weinberger","full_name":"Weinberger, Christian","first_name":"Christian"},{"first_name":"Markus","full_name":"Antonietti, Markus","last_name":"Antonietti"},{"first_name":"Mateusz","full_name":"Odziomek, Mateusz","last_name":"Odziomek"},{"last_name":"López‐Salas","full_name":"López‐Salas, Nieves","first_name":"Nieves"}]},{"user_id":"61189","title":"Die effektive Konjugationslänge ist für die spektrale Verschiebung im rot/grün schaltenden Cyanobakteriochrom Slr1393g3 verantwortlich","project":[{"_id":"52","name":"Computing Resources Provided by the Paderborn Center for Parallel Computing"}],"date_created":"2020-06-04T07:31:59Z","status":"public","publication_status":"published","publication_identifier":{"issn":["0044-8249"]},"keyword":["pc2-ressources"],"publication":"Angewandte Chemie","author":[{"last_name":"Wiebeler","full_name":"Wiebeler, Christian","first_name":"Christian"},{"full_name":"Rao, Aditya G.","first_name":"Aditya G.","last_name":"Rao"},{"first_name":"Wolfgang","full_name":"Gärtner, Wolfgang","last_name":"Gärtner"},{"last_name":"Schapiro","full_name":"Schapiro, Igor","first_name":"Igor"}],"doi":"10.1002/ange.201810266","_id":"17079","date_updated":"2022-01-06T06:53:04Z","language":[{"iso":"eng"}],"page":"1952-1957","citation":{"chicago":"Wiebeler, Christian, Aditya G. Rao, Wolfgang Gärtner, and Igor Schapiro. “Die Effektive Konjugationslänge Ist Für Die Spektrale Verschiebung Im Rot/Grün Schaltenden Cyanobakteriochrom Slr1393g3 Verantwortlich.” Angewandte Chemie, 2018, 1952–57. https://doi.org/10.1002/ange.201810266.","apa":"Wiebeler, C., Rao, A. G., Gärtner, W., & Schapiro, I. (2018). Die effektive Konjugationslänge ist für die spektrale Verschiebung im rot/grün schaltenden Cyanobakteriochrom Slr1393g3 verantwortlich. Angewandte Chemie, 1952–1957. https://doi.org/10.1002/ange.201810266","ama":"Wiebeler C, Rao AG, Gärtner W, Schapiro I. Die effektive Konjugationslänge ist für die spektrale Verschiebung im rot/grün schaltenden Cyanobakteriochrom Slr1393g3 verantwortlich. Angewandte Chemie. 2018:1952-1957. doi:10.1002/ange.201810266","bibtex":"@article{Wiebeler_Rao_Gärtner_Schapiro_2018, title={Die effektive Konjugationslänge ist für die spektrale Verschiebung im rot/grün schaltenden Cyanobakteriochrom Slr1393g3 verantwortlich}, DOI={10.1002/ange.201810266}, journal={Angewandte Chemie}, author={Wiebeler, Christian and Rao, Aditya G. and Gärtner, Wolfgang and Schapiro, Igor}, year={2018}, pages={1952–1957} }","mla":"Wiebeler, Christian, et al. “Die Effektive Konjugationslänge Ist Für Die Spektrale Verschiebung Im Rot/Grün Schaltenden Cyanobakteriochrom Slr1393g3 Verantwortlich.” Angewandte Chemie, 2018, pp. 1952–57, doi:10.1002/ange.201810266.","short":"C. Wiebeler, A.G. Rao, W. Gärtner, I. Schapiro, Angewandte Chemie (2018) 1952–1957.","ieee":"C. Wiebeler, A. G. Rao, W. Gärtner, and I. Schapiro, “Die effektive Konjugationslänge ist für die spektrale Verschiebung im rot/grün schaltenden Cyanobakteriochrom Slr1393g3 verantwortlich,” Angewandte Chemie, pp. 1952–1957, 2018."},"year":"2018","type":"journal_article"},{"date_updated":"2023-01-23T12:50:32Z","_id":"22242","doi":"10.1002/ange.201809275","language":[{"iso":"eng"}],"type":"journal_article","year":"2018","citation":{"bibtex":"@article{Stepen_Bursch_Grimme_Stephan_Paradies_2018, title={Reduktion von Phosphanoxiden mit Oxalylchlorid und Wasserstoff, vermittelt durch ein elektrophiles Phosphoniumkation}, DOI={10.1002/ange.201809275}, journal={Angewandte Chemie}, author={Stepen, Arne J. and Bursch, Markus and Grimme, Stefan and Stephan, Douglas W. and Paradies, Jan}, year={2018}, pages={15473–15476} }","mla":"Stepen, Arne J., et al. “Reduktion von Phosphanoxiden Mit Oxalylchlorid Und Wasserstoff, Vermittelt Durch Ein Elektrophiles Phosphoniumkation.” Angewandte Chemie, 2018, pp. 15473–76, doi:10.1002/ange.201809275.","ama":"Stepen AJ, Bursch M, Grimme S, Stephan DW, Paradies J. Reduktion von Phosphanoxiden mit Oxalylchlorid und Wasserstoff, vermittelt durch ein elektrophiles Phosphoniumkation. Angewandte Chemie. Published online 2018:15473-15476. doi:10.1002/ange.201809275","apa":"Stepen, A. J., Bursch, M., Grimme, S., Stephan, D. W., & Paradies, J. (2018). Reduktion von Phosphanoxiden mit Oxalylchlorid und Wasserstoff, vermittelt durch ein elektrophiles Phosphoniumkation. Angewandte Chemie, 15473–15476. https://doi.org/10.1002/ange.201809275","chicago":"Stepen, Arne J., Markus Bursch, Stefan Grimme, Douglas W. Stephan, and Jan Paradies. “Reduktion von Phosphanoxiden Mit Oxalylchlorid Und Wasserstoff, Vermittelt Durch Ein Elektrophiles Phosphoniumkation.” Angewandte Chemie, 2018, 15473–76. https://doi.org/10.1002/ange.201809275.","ieee":"A. J. Stepen, M. Bursch, S. Grimme, D. W. Stephan, and J. Paradies, “Reduktion von Phosphanoxiden mit Oxalylchlorid und Wasserstoff, vermittelt durch ein elektrophiles Phosphoniumkation,” Angewandte Chemie, pp. 15473–15476, 2018, doi: 10.1002/ange.201809275.","short":"A.J. Stepen, M. Bursch, S. Grimme, D.W. Stephan, J. Paradies, Angewandte Chemie (2018) 15473–15476."},"page":"15473-15476","user_id":"53339","title":"Reduktion von Phosphanoxiden mit Oxalylchlorid und Wasserstoff, vermittelt durch ein elektrophiles Phosphoniumkation","author":[{"full_name":"Stepen, Arne J.","first_name":"Arne J.","last_name":"Stepen"},{"last_name":"Bursch","full_name":"Bursch, Markus","first_name":"Markus"},{"first_name":"Stefan","full_name":"Grimme, Stefan","last_name":"Grimme"},{"full_name":"Stephan, Douglas W.","first_name":"Douglas W.","last_name":"Stephan"},{"orcid":"0000-0002-3698-668X","full_name":"Paradies, Jan","first_name":"Jan","id":"53339","last_name":"Paradies"}],"publication":"Angewandte Chemie","status":"public","date_created":"2021-05-26T10:42:23Z","publication_status":"published","publication_identifier":{"issn":["0044-8249","1521-3757"]}},{"title":"Auf dem Weg zur Smart Factory: modulare, intelligente Konzepte für die Produktion von Spezialchemikalien der Zukunft","publication_identifier":{"issn":["0044-8249","1521-3757"]},"publication_status":"published","doi":"10.1002/ange.201711571","date_updated":"2024-03-08T11:32:36Z","language":[{"iso":"eng"}],"user_id":"101499","abstract":[{"lang":"eng","text":"AbstractDie Digitalisierung und Flexibilisierung von Produktionsprozessen bieten in der Spezialchemie die Chance, auf marktseitige Herausforderungen adäquat zu reagieren. Kürzer werdende Produktlebenszyklen, zunehmende Produktindividualisierung und die daraus resultierende Volatilität der Märkte stellen neue Anforderungen an Anlagenbetreiber. Neuartige Konzepte wie modulare Produktionsanlagen sowie Technologieentwicklungen im Rahmen der Industrie 4.0 können dabei helfen, die Smart Factory in der Spezialchemie umzusetzen. Im Folgenden werden die für diesen Wandel notwendigen Konzepte vorgestellt."}],"extern":"1","date_created":"2023-10-04T14:19:19Z","status":"public","volume":130,"keyword":["General Medicine"],"publication":"Angewandte Chemie","quality_controlled":"1","author":[{"last_name":"Reitze","first_name":"Arnulf","full_name":"Reitze, Arnulf"},{"first_name":"Nikolas","full_name":"Jürgensmeyer, Nikolas","last_name":"Jürgensmeyer"},{"first_name":"Stefan","full_name":"Lier, Stefan","last_name":"Lier"},{"last_name":"Kohnke","first_name":"Marco","full_name":"Kohnke, Marco"},{"last_name":"Riese","id":"101499","first_name":"Julia","full_name":"Riese, Julia","orcid":"0000-0002-3053-0534"},{"full_name":"Grünewald, Marcus","first_name":"Marcus","last_name":"Grünewald"}],"publisher":"Wiley","issue":"16","intvolume":" 130","_id":"47584","page":"4318-4324","citation":{"mla":"Reitze, Arnulf, et al. “Auf Dem Weg Zur Smart Factory: Modulare, Intelligente Konzepte Für Die Produktion von Spezialchemikalien Der Zukunft.” Angewandte Chemie, vol. 130, no. 16, Wiley, 2018, pp. 4318–24, doi:10.1002/ange.201711571.","bibtex":"@article{Reitze_Jürgensmeyer_Lier_Kohnke_Riese_Grünewald_2018, title={Auf dem Weg zur Smart Factory: modulare, intelligente Konzepte für die Produktion von Spezialchemikalien der Zukunft}, volume={130}, DOI={10.1002/ange.201711571}, number={16}, journal={Angewandte Chemie}, publisher={Wiley}, author={Reitze, Arnulf and Jürgensmeyer, Nikolas and Lier, Stefan and Kohnke, Marco and Riese, Julia and Grünewald, Marcus}, year={2018}, pages={4318–4324} }","chicago":"Reitze, Arnulf, Nikolas Jürgensmeyer, Stefan Lier, Marco Kohnke, Julia Riese, and Marcus Grünewald. “Auf Dem Weg Zur Smart Factory: Modulare, Intelligente Konzepte Für Die Produktion von Spezialchemikalien Der Zukunft.” Angewandte Chemie 130, no. 16 (2018): 4318–24. https://doi.org/10.1002/ange.201711571.","ama":"Reitze A, Jürgensmeyer N, Lier S, Kohnke M, Riese J, Grünewald M. Auf dem Weg zur Smart Factory: modulare, intelligente Konzepte für die Produktion von Spezialchemikalien der Zukunft. Angewandte Chemie. 2018;130(16):4318-4324. doi:10.1002/ange.201711571","apa":"Reitze, A., Jürgensmeyer, N., Lier, S., Kohnke, M., Riese, J., & Grünewald, M. (2018). Auf dem Weg zur Smart Factory: modulare, intelligente Konzepte für die Produktion von Spezialchemikalien der Zukunft. Angewandte Chemie, 130(16), 4318–4324. https://doi.org/10.1002/ange.201711571","ieee":"A. Reitze, N. Jürgensmeyer, S. Lier, M. Kohnke, J. Riese, and M. Grünewald, “Auf dem Weg zur Smart Factory: modulare, intelligente Konzepte für die Produktion von Spezialchemikalien der Zukunft,” Angewandte Chemie, vol. 130, no. 16, pp. 4318–4324, 2018, doi: 10.1002/ange.201711571.","short":"A. Reitze, N. Jürgensmeyer, S. Lier, M. Kohnke, J. Riese, M. Grünewald, Angewandte Chemie 130 (2018) 4318–4324."},"type":"journal_article","year":"2018"},{"doi":"10.1002/ange.201511921","_id":"22253","date_updated":"2023-01-23T12:48:40Z","language":[{"iso":"eng"}],"year":"2016","type":"journal_article","citation":{"chicago":"Tamke, Sergej, Zheng-Wang Qu, Nikolai A. Sitte, Ulrich Flörke, Stefan Grimme, and Jan Paradies. “Cycloisomerisierung von 1,5-Eninen Über Eine 5-Endo-Dig- Cyclisierungs-Protodeborylierungs-Sequenz Mit Einem Frustrierten Lewis-Paar Als Katalysator.” Angewandte Chemie, 2016, 4408–11. https://doi.org/10.1002/ange.201511921.","ama":"Tamke S, Qu Z-W, Sitte NA, Flörke U, Grimme S, Paradies J. Cycloisomerisierung von 1,5-Eninen über eine 5-endo-dig- Cyclisierungs-Protodeborylierungs-Sequenz mit einem frustrierten Lewis-Paar als Katalysator. Angewandte Chemie. Published online 2016:4408-4411. doi:10.1002/ange.201511921","apa":"Tamke, S., Qu, Z.-W., Sitte, N. A., Flörke, U., Grimme, S., & Paradies, J. (2016). Cycloisomerisierung von 1,5-Eninen über eine 5-endo-dig- Cyclisierungs-Protodeborylierungs-Sequenz mit einem frustrierten Lewis-Paar als Katalysator. Angewandte Chemie, 4408–4411. https://doi.org/10.1002/ange.201511921","bibtex":"@article{Tamke_Qu_Sitte_Flörke_Grimme_Paradies_2016, title={Cycloisomerisierung von 1,5-Eninen über eine 5-endo-dig- Cyclisierungs-Protodeborylierungs-Sequenz mit einem frustrierten Lewis-Paar als Katalysator}, DOI={10.1002/ange.201511921}, journal={Angewandte Chemie}, author={Tamke, Sergej and Qu, Zheng-Wang and Sitte, Nikolai A. and Flörke, Ulrich and Grimme, Stefan and Paradies, Jan}, year={2016}, pages={4408–4411} }","mla":"Tamke, Sergej, et al. “Cycloisomerisierung von 1,5-Eninen Über Eine 5-Endo-Dig- Cyclisierungs-Protodeborylierungs-Sequenz Mit Einem Frustrierten Lewis-Paar Als Katalysator.” Angewandte Chemie, 2016, pp. 4408–11, doi:10.1002/ange.201511921.","short":"S. Tamke, Z.-W. Qu, N.A. Sitte, U. Flörke, S. Grimme, J. Paradies, Angewandte Chemie (2016) 4408–4411.","ieee":"S. Tamke, Z.-W. Qu, N. A. Sitte, U. Flörke, S. Grimme, and J. Paradies, “Cycloisomerisierung von 1,5-Eninen über eine 5-endo-dig- Cyclisierungs-Protodeborylierungs-Sequenz mit einem frustrierten Lewis-Paar als Katalysator,” Angewandte Chemie, pp. 4408–4411, 2016, doi: 10.1002/ange.201511921."},"page":"4408-4411","user_id":"53339","title":"Cycloisomerisierung von 1,5-Eninen über eine 5-endo-dig- Cyclisierungs-Protodeborylierungs-Sequenz mit einem frustrierten Lewis-Paar als Katalysator","status":"public","date_created":"2021-05-26T10:51:33Z","publication_identifier":{"issn":["0044-8249"]},"publication_status":"published","author":[{"last_name":"Tamke","first_name":"Sergej","full_name":"Tamke, Sergej"},{"first_name":"Zheng-Wang","full_name":"Qu, Zheng-Wang","last_name":"Qu"},{"first_name":"Nikolai A.","full_name":"Sitte, Nikolai A.","last_name":"Sitte"},{"first_name":"Ulrich","full_name":"Flörke, Ulrich","last_name":"Flörke"},{"last_name":"Grimme","full_name":"Grimme, Stefan","first_name":"Stefan"},{"orcid":"0000-0002-3698-668X","full_name":"Paradies, Jan","first_name":"Jan","id":"53339","last_name":"Paradies"}],"publication":"Angewandte Chemie"},{"language":[{"iso":"eng"}],"page":"12407-12411","type":"journal_article","year":"2016","citation":{"bibtex":"@article{Maier_Tussing_Schneider_Flörke_Qu_Grimme_Paradies_2016, title={Dehydrierende Oxidation von Indolinen und anderen Heterocyclen durch frustrierte Lewis-Paare}, DOI={10.1002/ange.201606426}, journal={Angewandte Chemie}, author={Maier, Alexander F. G. and Tussing, Sebastian and Schneider, Tobias and Flörke, Ulrich and Qu, Zheng-Wang and Grimme, Stefan and Paradies, Jan}, year={2016}, pages={12407–12411} }","mla":"Maier, Alexander F. G., et al. “Dehydrierende Oxidation von Indolinen Und Anderen Heterocyclen Durch Frustrierte Lewis-Paare.” Angewandte Chemie, 2016, pp. 12407–11, doi:10.1002/ange.201606426.","chicago":"Maier, Alexander F. G., Sebastian Tussing, Tobias Schneider, Ulrich Flörke, Zheng-Wang Qu, Stefan Grimme, and Jan Paradies. “Dehydrierende Oxidation von Indolinen Und Anderen Heterocyclen Durch Frustrierte Lewis-Paare.” Angewandte Chemie, 2016, 12407–11. https://doi.org/10.1002/ange.201606426.","ama":"Maier AFG, Tussing S, Schneider T, et al. Dehydrierende Oxidation von Indolinen und anderen Heterocyclen durch frustrierte Lewis-Paare. Angewandte Chemie. Published online 2016:12407-12411. doi:10.1002/ange.201606426","apa":"Maier, A. F. G., Tussing, S., Schneider, T., Flörke, U., Qu, Z.-W., Grimme, S., & Paradies, J. (2016). Dehydrierende Oxidation von Indolinen und anderen Heterocyclen durch frustrierte Lewis-Paare. Angewandte Chemie, 12407–12411. https://doi.org/10.1002/ange.201606426","ieee":"A. F. G. Maier et al., “Dehydrierende Oxidation von Indolinen und anderen Heterocyclen durch frustrierte Lewis-Paare,” Angewandte Chemie, pp. 12407–12411, 2016, doi: 10.1002/ange.201606426.","short":"A.F.G. Maier, S. Tussing, T. Schneider, U. Flörke, Z.-W. Qu, S. Grimme, J. Paradies, Angewandte Chemie (2016) 12407–12411."},"date_updated":"2023-01-23T12:48:16Z","_id":"22255","doi":"10.1002/ange.201606426","publication":"Angewandte Chemie","author":[{"first_name":"Alexander F. G.","full_name":"Maier, Alexander F. 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