[{"publisher":"Wiley","date_created":"2026-03-11T10:14:54Z","title":"Nichts zu lachen – oder doch?","issue":"1","year":"2026","language":[{"iso":"eng"}],"publication":"Nachrichten aus der Chemie","abstract":[{"lang":"eng","text":"<jats:title>Abstract</jats:title>\r\n                  <jats:p>Lachgas gelangt etwa aus Düngemitteln, Abgasen oder Narkosemitteln in die Atmosphäre und verursacht rund sechs Prozent der globalen Erwärmung. Effiziente Methoden, Lachgas abzubauen, gibt es bisher nicht. Wie ein neuer metallfreier Katalysator helfen könnte.</jats:p>"}],"date_updated":"2026-03-11T10:15:07Z","author":[{"full_name":"Paradies, Jan","id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan"}],"volume":74,"doi":"10.1002/nadc.20264154740","publication_status":"published","publication_identifier":{"issn":["1439-9598","1868-0054"]},"citation":{"ama":"Paradies J. Nichts zu lachen – oder doch? <i>Nachrichten aus der Chemie</i>. 2026;74(1):61-63. doi:<a href=\"https://doi.org/10.1002/nadc.20264154740\">10.1002/nadc.20264154740</a>","ieee":"J. Paradies, “Nichts zu lachen – oder doch?,” <i>Nachrichten aus der Chemie</i>, vol. 74, no. 1, pp. 61–63, 2026, doi: <a href=\"https://doi.org/10.1002/nadc.20264154740\">10.1002/nadc.20264154740</a>.","chicago":"Paradies, Jan. “Nichts Zu Lachen – Oder Doch?” <i>Nachrichten Aus Der Chemie</i> 74, no. 1 (2026): 61–63. <a href=\"https://doi.org/10.1002/nadc.20264154740\">https://doi.org/10.1002/nadc.20264154740</a>.","apa":"Paradies, J. (2026). Nichts zu lachen – oder doch? <i>Nachrichten Aus Der Chemie</i>, <i>74</i>(1), 61–63. <a href=\"https://doi.org/10.1002/nadc.20264154740\">https://doi.org/10.1002/nadc.20264154740</a>","short":"J. Paradies, Nachrichten Aus Der Chemie 74 (2026) 61–63.","bibtex":"@article{Paradies_2026, title={Nichts zu lachen – oder doch?}, volume={74}, DOI={<a href=\"https://doi.org/10.1002/nadc.20264154740\">10.1002/nadc.20264154740</a>}, number={1}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Paradies, Jan}, year={2026}, pages={61–63} }","mla":"Paradies, Jan. “Nichts Zu Lachen – Oder Doch?” <i>Nachrichten Aus Der Chemie</i>, vol. 74, no. 1, Wiley, 2026, pp. 61–63, doi:<a href=\"https://doi.org/10.1002/nadc.20264154740\">10.1002/nadc.20264154740</a>."},"page":"61-63","intvolume":"        74","_id":"64887","user_id":"53339","department":[{"_id":"2"},{"_id":"389"}],"type":"journal_article","status":"public"},{"doi":"10.1002/ejic.70158","title":"Double Functionalization of Atropisomeric Biphenyl Sulfoxides by                    <i>Ortho</i>                    ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids","author":[{"full_name":"Berreur, Jordan","last_name":"Berreur","first_name":"Jordan"},{"full_name":"Bortoluzzi, Julien","last_name":"Bortoluzzi","first_name":"Julien"},{"full_name":"Köring, Laura","last_name":"Köring","first_name":"Laura"},{"first_name":"Frédéric R.","last_name":"Leroux","full_name":"Leroux, Frédéric R."},{"first_name":"Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies","id":"53339","full_name":"Paradies, Jan"},{"full_name":"Panossian, Armen","last_name":"Panossian","first_name":"Armen"}],"date_created":"2026-03-11T10:10:08Z","date_updated":"2026-03-11T10:36:31Z","publisher":"Wiley","citation":{"ieee":"J. Berreur, J. Bortoluzzi, L. Köring, F. R. Leroux, J. Paradies, and A. Panossian, “Double Functionalization of Atropisomeric Biphenyl Sulfoxides by                    <i>Ortho</i>                    ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids,” <i>European Journal of Inorganic Chemistry</i>, Art. no. e70158, 2026, doi: <a href=\"https://doi.org/10.1002/ejic.70158\">10.1002/ejic.70158</a>.","chicago":"Berreur, Jordan, Julien Bortoluzzi, Laura Köring, Frédéric R. Leroux, Jan Paradies, and Armen Panossian. “Double Functionalization of Atropisomeric Biphenyl Sulfoxides by                    <i>Ortho</i>                    ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids.” <i>European Journal of Inorganic Chemistry</i>, 2026. <a href=\"https://doi.org/10.1002/ejic.70158\">https://doi.org/10.1002/ejic.70158</a>.","ama":"Berreur J, Bortoluzzi J, Köring L, Leroux FR, Paradies J, Panossian A. Double Functionalization of Atropisomeric Biphenyl Sulfoxides by                    <i>Ortho</i>                    ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids. <i>European Journal of Inorganic Chemistry</i>. Published online 2026. doi:<a href=\"https://doi.org/10.1002/ejic.70158\">10.1002/ejic.70158</a>","bibtex":"@article{Berreur_Bortoluzzi_Köring_Leroux_Paradies_Panossian_2026, title={Double Functionalization of Atropisomeric Biphenyl Sulfoxides by                    <i>Ortho</i>                    ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids}, DOI={<a href=\"https://doi.org/10.1002/ejic.70158\">10.1002/ejic.70158</a>}, number={e70158}, journal={European Journal of Inorganic Chemistry}, publisher={Wiley}, author={Berreur, Jordan and Bortoluzzi, Julien and Köring, Laura and Leroux, Frédéric R. and Paradies, Jan and Panossian, Armen}, year={2026} }","mla":"Berreur, Jordan, et al. “Double Functionalization of Atropisomeric Biphenyl Sulfoxides by                    <i>Ortho</i>                    ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids.” <i>European Journal of Inorganic Chemistry</i>, e70158, Wiley, 2026, doi:<a href=\"https://doi.org/10.1002/ejic.70158\">10.1002/ejic.70158</a>.","short":"J. Berreur, J. Bortoluzzi, L. Köring, F.R. Leroux, J. Paradies, A. Panossian, European Journal of Inorganic Chemistry (2026).","apa":"Berreur, J., Bortoluzzi, J., Köring, L., Leroux, F. R., Paradies, J., &#38; Panossian, A. (2026). Double Functionalization of Atropisomeric Biphenyl Sulfoxides by                    <i>Ortho</i>                    ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids. <i>European Journal of Inorganic Chemistry</i>, Article e70158. <a href=\"https://doi.org/10.1002/ejic.70158\">https://doi.org/10.1002/ejic.70158</a>"},"year":"2026","quality_controlled":"1","publication_identifier":{"issn":["1434-1948","1099-0682"]},"publication_status":"published","language":[{"iso":"eng"}],"article_number":"e70158","department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339","_id":"64886","status":"public","abstract":[{"text":"<jats:p>\r\n                    In the young field of enantioselective catalysis by frustrated Lewis pairs, the search for new chiral backbones for Lewis acids is desirable for future developments of the field. By taking advantage of the toluenesulfinyl group, a very useful traceless chiral auxiliary, it was possible to decorate stereopure axially chiral biphenyl tolyl sulfoxides and access unique chiral quaterphenyl tolyl sulfoxides by directed\r\n                    <jats:italic>ortho</jats:italic>\r\n                    ‐metalation and electrophile trapping as well as a dynamic kinetic asymmetric arylative cross‐coupling. The resulting chiral backbone is amenable to accessing chiral boron‐based Lewis acids by conversion of the sulfinyl group to boron‐based ones.\r\n                  </jats:p>","lang":"eng"}],"publication":"European Journal of Inorganic Chemistry","type":"journal_article"},{"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","id":"92677","full_name":"Medvaric, Viktorija","last_name":"Medvaric"},{"full_name":"Paradies, Jan","id":"53339","orcid":"0000-0002-3698-668X","last_name":"Paradies","first_name":"Jan"},{"orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"date_updated":"2025-11-10T08:44:04Z","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>","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} }","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>"},"year":"2025","publication_identifier":{"issn":["1615-4150","1615-4169"]},"publication_status":"published","language":[{"iso":"eng"}],"keyword":["T2","T","CSSD"],"article_number":"202500394","department":[{"_id":"2"},{"_id":"389"}],"user_id":"89271","_id":"61335","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"},{"publication":"Journal of the American Chemical Society","type":"journal_article","status":"public","department":[{"_id":"2"},{"_id":"389"}],"user_id":"89271","_id":"61336","language":[{"iso":"eng"}],"keyword":["T2","CSSD"],"article_number":"jacs.5c06190","publication_identifier":{"issn":["0002-7863","1520-5126"]},"publication_status":"published","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>","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} }","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>.","short":"R. Zhou, V. Medvaric, T. Werner, J. Paradies, Journal of the American Chemical Society (2025)."},"year":"2025","date_created":"2025-09-17T15:18:11Z","author":[{"last_name":"Zhou","full_name":"Zhou, Rundong","first_name":"Rundong"},{"first_name":"Viktorija","last_name":"Medvaric","id":"92677","full_name":"Medvaric, Viktorija"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","orcid":"https://orcid.org/0000-0001-9025-3244","last_name":"Werner"},{"first_name":"Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies","full_name":"Paradies, Jan","id":"53339"}],"publisher":"American Chemical Society (ACS)","date_updated":"2025-11-10T08:43:50Z","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"},{"publication":"European Journal of Organic Chemistry","type":"journal_article","status":"public","abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>We conducted an investigation into the palladium‐catalyzed carbon‐sulfur cross‐coupling reaction involving a 2‐bromothiophene derivative and potassium thioacetate as a substitute for hydrogen sulfide. This investigation utilized kinetic and computational methods. We synthesized two palladium complexes supported by the bisphosphane ligands bis(diphenylphosphino)ferrocene (DPPF) and bis(diisopropylphosphino)ferrocene (D<jats:italic>i</jats:italic>PPF), as well as their tentative intermediates in the catalytic cycle. Reaction rates were measured and then compared to computational predictions.</jats:p>","lang":"eng"}],"department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339","_id":"52541","language":[{"iso":"eng"}],"keyword":["Organic Chemistry","Physical and Theoretical Chemistry"],"issue":"8","publication_identifier":{"issn":["1434-193X","1099-0690"]},"publication_status":"published","intvolume":"        27","citation":{"ama":"Peschtrich S, Schoch R, Kuckling D, Paradies J. A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes. <i>European Journal of Organic Chemistry</i>. 2024;27(8). doi:<a href=\"https://doi.org/10.1002/ejoc.202301207\">10.1002/ejoc.202301207</a>","ieee":"S. Peschtrich, R. Schoch, D. Kuckling, and J. Paradies, “A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes,” <i>European Journal of Organic Chemistry</i>, vol. 27, no. 8, 2024, doi: <a href=\"https://doi.org/10.1002/ejoc.202301207\">10.1002/ejoc.202301207</a>.","chicago":"Peschtrich, Sebastian, Roland Schoch, Dirk Kuckling, and Jan Paradies. “A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes.” <i>European Journal of Organic Chemistry</i> 27, no. 8 (2024). <a href=\"https://doi.org/10.1002/ejoc.202301207\">https://doi.org/10.1002/ejoc.202301207</a>.","mla":"Peschtrich, Sebastian, et al. “A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes.” <i>European Journal of Organic Chemistry</i>, vol. 27, no. 8, Wiley, 2024, doi:<a href=\"https://doi.org/10.1002/ejoc.202301207\">10.1002/ejoc.202301207</a>.","short":"S. Peschtrich, R. Schoch, D. Kuckling, J. Paradies, European Journal of Organic Chemistry 27 (2024).","bibtex":"@article{Peschtrich_Schoch_Kuckling_Paradies_2024, title={A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes}, volume={27}, DOI={<a href=\"https://doi.org/10.1002/ejoc.202301207\">10.1002/ejoc.202301207</a>}, number={8}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Peschtrich, Sebastian and Schoch, Roland and Kuckling, Dirk and Paradies, Jan}, year={2024} }","apa":"Peschtrich, S., Schoch, R., Kuckling, D., &#38; Paradies, J. (2024). A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes. <i>European Journal of Organic Chemistry</i>, <i>27</i>(8). <a href=\"https://doi.org/10.1002/ejoc.202301207\">https://doi.org/10.1002/ejoc.202301207</a>"},"year":"2024","volume":27,"date_created":"2024-03-13T17:15:14Z","author":[{"first_name":"Sebastian","last_name":"Peschtrich","full_name":"Peschtrich, Sebastian"},{"first_name":"Roland","orcid":"0000-0003-2061-7289","last_name":"Schoch","id":"48467","full_name":"Schoch, Roland"},{"first_name":"Dirk","full_name":"Kuckling, Dirk","id":"287","last_name":"Kuckling"},{"first_name":"Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X","id":"53339","full_name":"Paradies, Jan"}],"publisher":"Wiley","date_updated":"2024-03-13T17:17:37Z","doi":"10.1002/ejoc.202301207","title":"A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes"},{"language":[{"iso":"eng"}],"keyword":["Inorganic Chemistry"],"department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339","_id":"52572","status":"public","abstract":[{"lang":"eng","text":"<jats:p>A series of substituted ferrocenyl boron derivatives was synthesized. The oxidation of the ferrocenyl unit resulted in a significant increase of the boron‐centered Lewis acidity. The neutral and cationic Lewis acids were characterized by NMR‐spectroscopy, crystal structure analysis and by computational methods. The new Lewis acids were then applied in the Meinwald rearrangement of epoxides, predominantly furnishing aldehydes as the kinetic products.</jats:p>"}],"publication":"European Journal of Inorganic Chemistry","type":"journal_article","doi":"10.1002/ejic.202400057","title":"Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements","date_created":"2024-03-14T07:09:09Z","author":[{"first_name":"Laura","last_name":"Köring","full_name":"Köring, Laura"},{"first_name":"Bernhard","full_name":"Birenheide, Bernhard","last_name":"Birenheide"},{"last_name":"Krämer","full_name":"Krämer, Felix","first_name":"Felix"},{"last_name":"Wenzel","full_name":"Wenzel, Jonas O.","first_name":"Jonas O."},{"first_name":"Roland","last_name":"Schoch","orcid":"0000-0003-2061-7289","full_name":"Schoch, Roland","id":"48467"},{"last_name":"Brehm","id":"100167","full_name":"Brehm, Martin","first_name":"Martin"},{"last_name":"Breher","full_name":"Breher, Frank","first_name":"Frank"},{"first_name":"Jan","full_name":"Paradies, Jan","id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X"}],"publisher":"Wiley","date_updated":"2024-03-14T07:10:37Z","citation":{"ieee":"L. Köring <i>et al.</i>, “Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements,” <i>European Journal of Inorganic Chemistry</i>, 2024, doi: <a href=\"https://doi.org/10.1002/ejic.202400057\">10.1002/ejic.202400057</a>.","chicago":"Köring, Laura, Bernhard Birenheide, Felix Krämer, Jonas O. Wenzel, Roland Schoch, Martin Brehm, Frank Breher, and Jan Paradies. “Synthesis of Ferrocenyl Boranes and Their Application as Lewis Acids in Epoxide Rearrangements.” <i>European Journal of Inorganic Chemistry</i>, 2024. <a href=\"https://doi.org/10.1002/ejic.202400057\">https://doi.org/10.1002/ejic.202400057</a>.","ama":"Köring L, Birenheide B, Krämer F, et al. Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements. <i>European Journal of Inorganic Chemistry</i>. Published online 2024. doi:<a href=\"https://doi.org/10.1002/ejic.202400057\">10.1002/ejic.202400057</a>","apa":"Köring, L., Birenheide, B., Krämer, F., Wenzel, J. O., Schoch, R., Brehm, M., Breher, F., &#38; Paradies, J. (2024). Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements. <i>European Journal of Inorganic Chemistry</i>. <a href=\"https://doi.org/10.1002/ejic.202400057\">https://doi.org/10.1002/ejic.202400057</a>","bibtex":"@article{Köring_Birenheide_Krämer_Wenzel_Schoch_Brehm_Breher_Paradies_2024, title={Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements}, DOI={<a href=\"https://doi.org/10.1002/ejic.202400057\">10.1002/ejic.202400057</a>}, journal={European Journal of Inorganic Chemistry}, publisher={Wiley}, author={Köring, Laura and Birenheide, Bernhard and Krämer, Felix and Wenzel, Jonas O. and Schoch, Roland and Brehm, Martin and Breher, Frank and Paradies, Jan}, year={2024} }","short":"L. Köring, B. Birenheide, F. Krämer, J.O. Wenzel, R. Schoch, M. Brehm, F. Breher, J. Paradies, European Journal of Inorganic Chemistry (2024).","mla":"Köring, Laura, et al. “Synthesis of Ferrocenyl Boranes and Their Application as Lewis Acids in Epoxide Rearrangements.” <i>European Journal of Inorganic Chemistry</i>, Wiley, 2024, doi:<a href=\"https://doi.org/10.1002/ejic.202400057\">10.1002/ejic.202400057</a>."},"year":"2024","publication_identifier":{"issn":["1434-1948","1099-0682"]},"publication_status":"published"},{"_id":"55371","user_id":"53339","department":[{"_id":"2"},{"_id":"389"}],"language":[{"iso":"eng"}],"type":"journal_article","publication":"Advanced Synthesis &amp; Catalysis","abstract":[{"lang":"eng","text":"<jats:title>Abstract</jats:title><jats:p>The activation of C(<jats:italic>sp</jats:italic><jats:sup>3</jats:sup>)−F bonds by the commercially available catalyst B(C<jats:sub>6</jats:sub>F<jats:sub>5</jats:sub>)<jats:sub>3</jats:sub> is reported and applied in reactions with arenes, allylic, vinylic and acetylenic silanes, and olefins to achieve a variety of C−C bond formations (45 examples).</jats:p>"}],"status":"public","date_updated":"2024-07-24T09:18:18Z","publisher":"Wiley","date_created":"2024-07-24T09:16:15Z","author":[{"full_name":"Hoppe, Axel","last_name":"Hoppe","first_name":"Axel"},{"first_name":"Arne J.","full_name":"Stepen, Arne J.","last_name":"Stepen"},{"first_name":"Laura","last_name":"Köring","full_name":"Köring, Laura"},{"last_name":"Paradies","orcid":"0000-0002-3698-668X","full_name":"Paradies, Jan","id":"53339","first_name":"Jan"}],"volume":366,"title":"Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds","doi":"10.1002/adsc.202400511","publication_status":"published","publication_identifier":{"issn":["1615-4150","1615-4169"]},"issue":"13","year":"2024","citation":{"ieee":"A. Hoppe, A. J. Stepen, L. Köring, and J. Paradies, “Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds,” <i>Advanced Synthesis &#38;amp; Catalysis</i>, vol. 366, no. 13, pp. 2933–2938, 2024, doi: <a href=\"https://doi.org/10.1002/adsc.202400511\">10.1002/adsc.202400511</a>.","chicago":"Hoppe, Axel, Arne J. Stepen, Laura Köring, and Jan Paradies. “Tris(Pentafluorophenyl)Borane‐Catalyzed Functionalization of Benzylic C−F Bonds.” <i>Advanced Synthesis &#38;amp; Catalysis</i> 366, no. 13 (2024): 2933–38. <a href=\"https://doi.org/10.1002/adsc.202400511\">https://doi.org/10.1002/adsc.202400511</a>.","ama":"Hoppe A, Stepen AJ, Köring L, Paradies J. Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds. <i>Advanced Synthesis &#38;amp; Catalysis</i>. 2024;366(13):2933-2938. doi:<a href=\"https://doi.org/10.1002/adsc.202400511\">10.1002/adsc.202400511</a>","bibtex":"@article{Hoppe_Stepen_Köring_Paradies_2024, title={Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds}, volume={366}, DOI={<a href=\"https://doi.org/10.1002/adsc.202400511\">10.1002/adsc.202400511</a>}, number={13}, journal={Advanced Synthesis &#38;amp; Catalysis}, publisher={Wiley}, author={Hoppe, Axel and Stepen, Arne J. and Köring, Laura and Paradies, Jan}, year={2024}, pages={2933–2938} }","mla":"Hoppe, Axel, et al. “Tris(Pentafluorophenyl)Borane‐Catalyzed Functionalization of Benzylic C−F Bonds.” <i>Advanced Synthesis &#38;amp; Catalysis</i>, vol. 366, no. 13, Wiley, 2024, pp. 2933–38, doi:<a href=\"https://doi.org/10.1002/adsc.202400511\">10.1002/adsc.202400511</a>.","short":"A. Hoppe, A.J. Stepen, L. Köring, J. Paradies, Advanced Synthesis &#38;amp; Catalysis 366 (2024) 2933–2938.","apa":"Hoppe, A., Stepen, A. J., Köring, L., &#38; Paradies, J. (2024). Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds. <i>Advanced Synthesis &#38;amp; Catalysis</i>, <i>366</i>(13), 2933–2938. <a href=\"https://doi.org/10.1002/adsc.202400511\">https://doi.org/10.1002/adsc.202400511</a>"},"page":"2933-2938","intvolume":"       366"},{"publisher":"Wiley","date_created":"2025-04-22T05:59:08Z","title":"Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds","quality_controlled":"1","issue":"13","year":"2024","keyword":["fluoride","bond activation","borane","Lewis acid","C-C bond formation"],"language":[{"iso":"eng"}],"publication":"Advanced Synthesis &amp; Catalysis","abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>The activation of C(<jats:italic>sp</jats:italic><jats:sup>3</jats:sup>)−F bonds by the commercially available catalyst B(C<jats:sub>6</jats:sub>F<jats:sub>5</jats:sub>)<jats:sub>3</jats:sub> is reported and applied in reactions with arenes, allylic, vinylic and acetylenic silanes, and olefins to achieve a variety of C−C bond formations (45 examples).</jats:p>","lang":"eng"}],"date_updated":"2025-04-22T06:11:59Z","oa":"1","author":[{"id":"62844","full_name":"Hoppe, Axel","last_name":"Hoppe","first_name":"Axel"},{"first_name":"Arne J.","last_name":"Stepen","full_name":"Stepen, Arne J."},{"last_name":"Köring","full_name":"Köring, Laura","first_name":"Laura"},{"first_name":"Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X","id":"53339","full_name":"Paradies, Jan"}],"volume":366,"main_file_link":[{"url":"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adsc.202400511","open_access":"1"}],"doi":"10.1002/adsc.202400511","publication_status":"published","publication_identifier":{"issn":["1615-4150","1615-4169"]},"citation":{"apa":"Hoppe, A., Stepen, A. J., Köring, L., &#38; Paradies, J. (2024). Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds. <i>Advanced Synthesis &#38;amp; Catalysis</i>, <i>366</i>(13), 2933–2938. <a href=\"https://doi.org/10.1002/adsc.202400511\">https://doi.org/10.1002/adsc.202400511</a>","mla":"Hoppe, Axel, et al. “Tris(Pentafluorophenyl)Borane‐Catalyzed Functionalization of Benzylic C−F Bonds.” <i>Advanced Synthesis &#38;amp; Catalysis</i>, vol. 366, no. 13, Wiley, 2024, pp. 2933–38, doi:<a href=\"https://doi.org/10.1002/adsc.202400511\">10.1002/adsc.202400511</a>.","bibtex":"@article{Hoppe_Stepen_Köring_Paradies_2024, title={Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds}, volume={366}, DOI={<a href=\"https://doi.org/10.1002/adsc.202400511\">10.1002/adsc.202400511</a>}, number={13}, journal={Advanced Synthesis &#38;amp; Catalysis}, publisher={Wiley}, author={Hoppe, Axel and Stepen, Arne J. and Köring, Laura and Paradies, Jan}, year={2024}, pages={2933–2938} }","short":"A. Hoppe, A.J. Stepen, L. Köring, J. Paradies, Advanced Synthesis &#38;amp; Catalysis 366 (2024) 2933–2938.","ama":"Hoppe A, Stepen AJ, Köring L, Paradies J. Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds. <i>Advanced Synthesis &#38;amp; Catalysis</i>. 2024;366(13):2933-2938. doi:<a href=\"https://doi.org/10.1002/adsc.202400511\">10.1002/adsc.202400511</a>","ieee":"A. Hoppe, A. J. Stepen, L. Köring, and J. Paradies, “Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds,” <i>Advanced Synthesis &#38;amp; Catalysis</i>, vol. 366, no. 13, pp. 2933–2938, 2024, doi: <a href=\"https://doi.org/10.1002/adsc.202400511\">10.1002/adsc.202400511</a>.","chicago":"Hoppe, Axel, Arne J. Stepen, Laura Köring, and Jan Paradies. “Tris(Pentafluorophenyl)Borane‐Catalyzed Functionalization of Benzylic C−F Bonds.” <i>Advanced Synthesis &#38;amp; Catalysis</i> 366, no. 13 (2024): 2933–38. <a href=\"https://doi.org/10.1002/adsc.202400511\">https://doi.org/10.1002/adsc.202400511</a>."},"page":"2933-2938","intvolume":"       366","_id":"59616","user_id":"62844","department":[{"_id":"389"}],"type":"journal_article","status":"public"},{"citation":{"apa":"Krämer, F., Paradies, J., Fernández, I., &#38; Breher, F. (2023). A crystalline aluminium–carbon-based ambiphile capable of activation and catalytic transfer of ammonia in non-aqueous media. <i>Nature Chemistry</i>. <a href=\"https://doi.org/10.1038/s41557-023-01340-9\">https://doi.org/10.1038/s41557-023-01340-9</a>","short":"F. Krämer, J. Paradies, I. Fernández, F. Breher, Nature Chemistry (2023).","bibtex":"@article{Krämer_Paradies_Fernández_Breher_2023, title={A crystalline aluminium–carbon-based ambiphile capable of activation and catalytic transfer of ammonia in non-aqueous media}, DOI={<a href=\"https://doi.org/10.1038/s41557-023-01340-9\">10.1038/s41557-023-01340-9</a>}, journal={Nature Chemistry}, publisher={Springer Science and Business Media LLC}, author={Krämer, Felix and Paradies, Jan and Fernández, Israel and Breher, Frank}, year={2023} }","mla":"Krämer, Felix, et al. “A Crystalline Aluminium–Carbon-Based Ambiphile Capable of Activation and Catalytic Transfer of Ammonia in Non-Aqueous Media.” <i>Nature Chemistry</i>, Springer Science and Business Media LLC, 2023, doi:<a href=\"https://doi.org/10.1038/s41557-023-01340-9\">10.1038/s41557-023-01340-9</a>.","ieee":"F. Krämer, J. Paradies, I. Fernández, and F. Breher, “A crystalline aluminium–carbon-based ambiphile capable of activation and catalytic transfer of ammonia in non-aqueous media,” <i>Nature Chemistry</i>, 2023, doi: <a href=\"https://doi.org/10.1038/s41557-023-01340-9\">10.1038/s41557-023-01340-9</a>.","chicago":"Krämer, Felix, Jan Paradies, Israel Fernández, and Frank Breher. “A Crystalline Aluminium–Carbon-Based Ambiphile Capable of Activation and Catalytic Transfer of Ammonia in Non-Aqueous Media.” <i>Nature Chemistry</i>, 2023. <a href=\"https://doi.org/10.1038/s41557-023-01340-9\">https://doi.org/10.1038/s41557-023-01340-9</a>.","ama":"Krämer F, Paradies J, Fernández I, Breher F. A crystalline aluminium–carbon-based ambiphile capable of activation and catalytic transfer of ammonia in non-aqueous media. <i>Nature Chemistry</i>. Published online 2023. doi:<a href=\"https://doi.org/10.1038/s41557-023-01340-9\">10.1038/s41557-023-01340-9</a>"},"year":"2023","publication_identifier":{"issn":["1755-4330","1755-4349"]},"publication_status":"published","doi":"10.1038/s41557-023-01340-9","title":"A crystalline aluminium–carbon-based ambiphile capable of activation and catalytic transfer of ammonia in non-aqueous media","date_created":"2023-10-04T14:40:07Z","author":[{"first_name":"Felix","full_name":"Krämer, Felix","last_name":"Krämer"},{"first_name":"Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies","full_name":"Paradies, Jan","id":"53339"},{"full_name":"Fernández, Israel","last_name":"Fernández","first_name":"Israel"},{"first_name":"Frank","full_name":"Breher, Frank","last_name":"Breher"}],"date_updated":"2023-10-04T14:41:12Z","publisher":"Springer Science and Business Media LLC","status":"public","publication":"Nature Chemistry","type":"journal_article","language":[{"iso":"eng"}],"keyword":["General Chemical Engineering","General Chemistry"],"department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339","_id":"47589"},{"user_id":"53339","department":[{"_id":"2"},{"_id":"389"}],"_id":"52542","language":[{"iso":"eng"}],"keyword":["General Chemistry","Catalysis","Organic Chemistry"],"type":"journal_article","publication":"Chemistry – A European Journal","status":"public","abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>We report on so‐called “hidden FLPs” (FLP: frustrated Lewis pair) consisting of a phosphorus ylide featuring a group 13 fragment in the <jats:italic>ortho</jats:italic> position of a phenyl ring scaffold to form five‐membered ring structures. Although the formation of the Lewis acid/base adducts was observed in the solid state, most of the title compounds readily react with carbon dioxide to provide stable insertion products. Strikingly, 0.3–3.0 mol% of the reported aluminum and gallium/carbon‐based ambiphiles catalyze the reduction of CO<jats:sub>2</jats:sub> to methanol with satisfactory high selectivity and yields using pinacol borane as stoichiometric reduction equivalent. Comprehensive computational studies provided valuable mechanistic insights and shed more light on activity differences.</jats:p>","lang":"eng"}],"author":[{"first_name":"Felix","full_name":"Krämer, Felix","last_name":"Krämer"},{"full_name":"Paradies, Jan","id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan"},{"first_name":"Israel","last_name":"Fernández","full_name":"Fernández, Israel"},{"full_name":"Breher, Frank","last_name":"Breher","first_name":"Frank"}],"date_created":"2024-03-13T17:17:52Z","volume":30,"publisher":"Wiley","date_updated":"2024-03-13T17:18:17Z","doi":"10.1002/chem.202303380","title":"Quo Vadis CO<sub>2</sub> Activation: Catalytic Reduction of CO<sub>2</sub> to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles","issue":"5","publication_status":"published","publication_identifier":{"issn":["0947-6539","1521-3765"]},"citation":{"chicago":"Krämer, Felix, Jan Paradies, Israel Fernández, and Frank Breher. “Quo Vadis CO<sub>2</sub> Activation: Catalytic Reduction of CO<sub>2</sub> to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles.” <i>Chemistry – A European Journal</i> 30, no. 5 (2023). <a href=\"https://doi.org/10.1002/chem.202303380\">https://doi.org/10.1002/chem.202303380</a>.","ieee":"F. Krämer, J. Paradies, I. Fernández, and F. Breher, “Quo Vadis CO<sub>2</sub> Activation: Catalytic Reduction of CO<sub>2</sub> to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles,” <i>Chemistry – A European Journal</i>, vol. 30, no. 5, 2023, doi: <a href=\"https://doi.org/10.1002/chem.202303380\">10.1002/chem.202303380</a>.","ama":"Krämer F, Paradies J, Fernández I, Breher F. Quo Vadis CO<sub>2</sub> Activation: Catalytic Reduction of CO<sub>2</sub> to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles. <i>Chemistry – A European Journal</i>. 2023;30(5). doi:<a href=\"https://doi.org/10.1002/chem.202303380\">10.1002/chem.202303380</a>","bibtex":"@article{Krämer_Paradies_Fernández_Breher_2023, title={Quo Vadis CO<sub>2</sub> Activation: Catalytic Reduction of CO<sub>2</sub> to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles}, volume={30}, DOI={<a href=\"https://doi.org/10.1002/chem.202303380\">10.1002/chem.202303380</a>}, number={5}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Krämer, Felix and Paradies, Jan and Fernández, Israel and Breher, Frank}, year={2023} }","mla":"Krämer, Felix, et al. “Quo Vadis CO<sub>2</sub> Activation: Catalytic Reduction of CO<sub>2</sub> to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles.” <i>Chemistry – A European Journal</i>, vol. 30, no. 5, Wiley, 2023, doi:<a href=\"https://doi.org/10.1002/chem.202303380\">10.1002/chem.202303380</a>.","short":"F. Krämer, J. Paradies, I. Fernández, F. Breher, Chemistry – A European Journal 30 (2023).","apa":"Krämer, F., Paradies, J., Fernández, I., &#38; Breher, F. (2023). Quo Vadis CO<sub>2</sub> Activation: Catalytic Reduction of CO<sub>2</sub> to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles. <i>Chemistry – A European Journal</i>, <i>30</i>(5). <a href=\"https://doi.org/10.1002/chem.202303380\">https://doi.org/10.1002/chem.202303380</a>"},"intvolume":"        30","year":"2023"},{"doi":"10.1002/anie.202301632","title":"Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation","author":[{"first_name":"Laura","full_name":"Köring, Laura","last_name":"Köring"},{"last_name":"Stepen","full_name":"Stepen, Arne","first_name":"Arne"},{"first_name":"Bernhard","last_name":"Birenheide","full_name":"Birenheide, Bernhard"},{"first_name":"Simon","last_name":"Barth","full_name":"Barth, Simon"},{"full_name":"Leskov, Maxim","last_name":"Leskov","first_name":"Maxim"},{"first_name":"Roland","last_name":"Schoch","full_name":"Schoch, Roland"},{"first_name":"Felix","full_name":"Krämer, Felix","last_name":"Krämer"},{"last_name":"Breher","full_name":"Breher, Frank","first_name":"Frank"},{"id":"53339","full_name":"Paradies, Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan"}],"date_created":"2023-03-08T19:27:25Z","date_updated":"2023-03-08T19:31:59Z","publisher":"Wiley","citation":{"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. <i>Angewandte Chemie International Edition</i>. Published online 2023. doi:<a href=\"https://doi.org/10.1002/anie.202301632\">10.1002/anie.202301632</a>","ieee":"L. Köring <i>et al.</i>, “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation,” <i>Angewandte Chemie International Edition</i>, 2023, doi: <a href=\"https://doi.org/10.1002/anie.202301632\">10.1002/anie.202301632</a>.","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.” <i>Angewandte Chemie International Edition</i>, 2023. <a href=\"https://doi.org/10.1002/anie.202301632\">https://doi.org/10.1002/anie.202301632</a>.","apa":"Köring, L., Stepen, A., Birenheide, B., Barth, S., Leskov, M., Schoch, R., Krämer, F., Breher, F., &#38; Paradies, J. (2023). Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation. <i>Angewandte Chemie International Edition</i>. <a href=\"https://doi.org/10.1002/anie.202301632\">https://doi.org/10.1002/anie.202301632</a>","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={<a href=\"https://doi.org/10.1002/anie.202301632\">10.1002/anie.202301632</a>}, journal={Angewandte Chemie International Edition}, 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} }","short":"L. Köring, A. Stepen, B. Birenheide, S. Barth, M. Leskov, R. Schoch, F. Krämer, F. Breher, J. Paradies, Angewandte Chemie International Edition (2023).","mla":"Köring, Laura, et al. “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation.” <i>Angewandte Chemie International Edition</i>, Wiley, 2023, doi:<a href=\"https://doi.org/10.1002/anie.202301632\">10.1002/anie.202301632</a>."},"year":"2023","publication_identifier":{"issn":["1433-7851","1521-3773"]},"publication_status":"published","language":[{"iso":"eng"}],"keyword":["General Chemistry","Catalysis"],"department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339","_id":"42878","status":"public","publication":"Angewandte Chemie International Edition","type":"journal_article"},{"type":"journal_article","publication":"Angewandte Chemie","status":"public","_id":"42879","user_id":"53339","department":[{"_id":"2"},{"_id":"389"}],"keyword":["General Medicine"],"language":[{"iso":"eng"}],"publication_status":"published","publication_identifier":{"issn":["0044-8249","1521-3757"]},"year":"2023","citation":{"apa":"Köring, L., Stepen, A., Birenheide, B., Barth, S., Leskov, M., Schoch, R., Krämer, F., Breher, F., &#38; Paradies, J. (2023). Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation. <i>Angewandte Chemie</i>. <a href=\"https://doi.org/10.1002/ange.202301632\">https://doi.org/10.1002/ange.202301632</a>","mla":"Köring, Laura, et al. “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation.” <i>Angewandte Chemie</i>, Wiley, 2023, doi:<a href=\"https://doi.org/10.1002/ange.202301632\">10.1002/ange.202301632</a>.","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={<a href=\"https://doi.org/10.1002/ange.202301632\">10.1002/ange.202301632</a>}, 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} }","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 <i>et al.</i>, “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation,” <i>Angewandte Chemie</i>, 2023, doi: <a href=\"https://doi.org/10.1002/ange.202301632\">10.1002/ange.202301632</a>.","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.” <i>Angewandte Chemie</i>, 2023. <a href=\"https://doi.org/10.1002/ange.202301632\">https://doi.org/10.1002/ange.202301632</a>.","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. <i>Angewandte Chemie</i>. Published online 2023. doi:<a href=\"https://doi.org/10.1002/ange.202301632\">10.1002/ange.202301632</a>"},"publisher":"Wiley","date_updated":"2023-03-08T19:32:09Z","date_created":"2023-03-08T19:31:03Z","author":[{"last_name":"Köring","full_name":"Köring, Laura","first_name":"Laura"},{"first_name":"Arne","full_name":"Stepen, Arne","last_name":"Stepen"},{"last_name":"Birenheide","full_name":"Birenheide, Bernhard","first_name":"Bernhard"},{"last_name":"Barth","full_name":"Barth, Simon","first_name":"Simon"},{"first_name":"Maxim","last_name":"Leskov","full_name":"Leskov, Maxim"},{"last_name":"Schoch","full_name":"Schoch, Roland","first_name":"Roland"},{"last_name":"Krämer","full_name":"Krämer, Felix","first_name":"Felix"},{"first_name":"Frank","last_name":"Breher","full_name":"Breher, Frank"},{"full_name":"Paradies, Jan","id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan"}],"title":"Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation","doi":"10.1002/ange.202301632"},{"year":"2023","issue":"7","title":"Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations","publisher":"American Chemical Society (ACS)","date_created":"2023-05-05T13:25:50Z","publication":"Accounts of Chemical Research","keyword":["General Medicine","General Chemistry"],"language":[{"iso":"eng"}],"intvolume":"        56","page":"821-834","citation":{"short":"J. Paradies, Accounts of Chemical Research 56 (2023) 821–834.","mla":"Paradies, Jan. “Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations.” <i>Accounts of Chemical Research</i>, vol. 56, no. 7, American Chemical Society (ACS), 2023, pp. 821–34, doi:<a href=\"https://doi.org/10.1021/acs.accounts.2c00832\">10.1021/acs.accounts.2c00832</a>.","bibtex":"@article{Paradies_2023, title={Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations}, volume={56}, DOI={<a href=\"https://doi.org/10.1021/acs.accounts.2c00832\">10.1021/acs.accounts.2c00832</a>}, number={7}, journal={Accounts of Chemical Research}, publisher={American Chemical Society (ACS)}, author={Paradies, Jan}, year={2023}, pages={821–834} }","apa":"Paradies, J. (2023). Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations. <i>Accounts of Chemical Research</i>, <i>56</i>(7), 821–834. <a href=\"https://doi.org/10.1021/acs.accounts.2c00832\">https://doi.org/10.1021/acs.accounts.2c00832</a>","ama":"Paradies J. Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations. <i>Accounts of Chemical Research</i>. 2023;56(7):821-834. doi:<a href=\"https://doi.org/10.1021/acs.accounts.2c00832\">10.1021/acs.accounts.2c00832</a>","ieee":"J. Paradies, “Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations,” <i>Accounts of Chemical Research</i>, vol. 56, no. 7, pp. 821–834, 2023, doi: <a href=\"https://doi.org/10.1021/acs.accounts.2c00832\">10.1021/acs.accounts.2c00832</a>.","chicago":"Paradies, Jan. “Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations.” <i>Accounts of Chemical Research</i> 56, no. 7 (2023): 821–34. <a href=\"https://doi.org/10.1021/acs.accounts.2c00832\">https://doi.org/10.1021/acs.accounts.2c00832</a>."},"publication_identifier":{"issn":["0001-4842","1520-4898"]},"publication_status":"published","doi":"10.1021/acs.accounts.2c00832","date_updated":"2023-05-05T13:27:06Z","volume":56,"author":[{"first_name":"Jan","id":"53339","full_name":"Paradies, Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies"}],"status":"public","type":"journal_article","_id":"44523","department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339"},{"author":[{"last_name":"Sieland","full_name":"Sieland, Benedikt","first_name":"Benedikt"},{"last_name":"Stahn","full_name":"Stahn, Marcel","first_name":"Marcel"},{"last_name":"Schoch","full_name":"Schoch, Roland","first_name":"Roland"},{"last_name":"Daniliuc","full_name":"Daniliuc, Constantin","first_name":"Constantin"},{"first_name":"Sebastian","last_name":"Spicher","full_name":"Spicher, Sebastian"},{"last_name":"Grimme","full_name":"Grimme, Stefan","first_name":"Stefan"},{"first_name":"Andreas","full_name":"Hansen, Andreas","last_name":"Hansen"},{"first_name":"Jan","full_name":"Paradies, Jan","id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X"}],"date_created":"2023-08-03T09:00:33Z","date_updated":"2023-08-03T09:01:41Z","publisher":"Wiley","doi":"10.1002/anie.202308752","title":"Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs","publication_status":"published","publication_identifier":{"issn":["1433-7851","1521-3773"]},"citation":{"ama":"Sieland B, Stahn M, Schoch R, et al. Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs. <i>Angewandte Chemie International Edition</i>. Published online 2023. doi:<a href=\"https://doi.org/10.1002/anie.202308752\">10.1002/anie.202308752</a>","ieee":"B. Sieland <i>et al.</i>, “Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs,” <i>Angewandte Chemie International Edition</i>, 2023, doi: <a href=\"https://doi.org/10.1002/anie.202308752\">10.1002/anie.202308752</a>.","chicago":"Sieland, Benedikt, Marcel Stahn, Roland Schoch, Constantin Daniliuc, Sebastian Spicher, Stefan Grimme, Andreas Hansen, and Jan Paradies. “Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs.” <i>Angewandte Chemie International Edition</i>, 2023. <a href=\"https://doi.org/10.1002/anie.202308752\">https://doi.org/10.1002/anie.202308752</a>.","short":"B. Sieland, M. Stahn, R. Schoch, C. Daniliuc, S. Spicher, S. Grimme, A. Hansen, J. Paradies, Angewandte Chemie International Edition (2023).","bibtex":"@article{Sieland_Stahn_Schoch_Daniliuc_Spicher_Grimme_Hansen_Paradies_2023, title={Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs}, DOI={<a href=\"https://doi.org/10.1002/anie.202308752\">10.1002/anie.202308752</a>}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Sieland, Benedikt and Stahn, Marcel and Schoch, Roland and Daniliuc, Constantin and Spicher, Sebastian and Grimme, Stefan and Hansen, Andreas and Paradies, Jan}, year={2023} }","mla":"Sieland, Benedikt, et al. “Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs.” <i>Angewandte Chemie International Edition</i>, Wiley, 2023, doi:<a href=\"https://doi.org/10.1002/anie.202308752\">10.1002/anie.202308752</a>.","apa":"Sieland, B., Stahn, M., Schoch, R., Daniliuc, C., Spicher, S., Grimme, S., Hansen, A., &#38; Paradies, J. (2023). Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs. <i>Angewandte Chemie International Edition</i>. <a href=\"https://doi.org/10.1002/anie.202308752\">https://doi.org/10.1002/anie.202308752</a>"},"year":"2023","user_id":"53339","department":[{"_id":"2"},{"_id":"389"}],"_id":"46277","language":[{"iso":"eng"}],"keyword":["General Chemistry","Catalysis"],"type":"journal_article","publication":"Angewandte Chemie International Edition","status":"public"},{"status":"public","abstract":[{"lang":"eng","text":"<jats:title>Abstract</jats:title><jats:p>The synthesis of three novel imidazolyl‐substituted sulfur‐containing heteroacenes is reported. These heteroacenes consisting of annelated benzo‐ and naphthothiophenes serve as precursors for the generation of open‐shell quinoid heteroacenes by oxidation with alkaline ferric cyanide. Spectroscopic and computational experiments support the formation of reactive open‐shell quinoids, which, however, quickly produce paramagnetic polymeric material.</jats:p>"}],"publication":"ChemistryOpen","type":"journal_article","language":[{"iso":"eng"}],"article_number":"e202300003","department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339","_id":"64893","intvolume":"        12","citation":{"ama":"Hou P, Peschtrich S, Feuerstein W, et al. Imidazolyl‐Substituted Benzo‐ and Naphthodithiophenes as Precursors for the Synthesis of Transient Open‐Shell Quinoids. <i>ChemistryOpen</i>. 2023;12(11). doi:<a href=\"https://doi.org/10.1002/open.202300003\">10.1002/open.202300003</a>","ieee":"P. Hou <i>et al.</i>, “Imidazolyl‐Substituted Benzo‐ and Naphthodithiophenes as Precursors for the Synthesis of Transient Open‐Shell Quinoids,” <i>ChemistryOpen</i>, vol. 12, no. 11, Art. no. e202300003, 2023, doi: <a href=\"https://doi.org/10.1002/open.202300003\">10.1002/open.202300003</a>.","chicago":"Hou, Peng, Sebastian Peschtrich, Wolfram Feuerstein, Roland Schoch, Stephan Hohloch, Frank Breher, and Jan Paradies. “Imidazolyl‐Substituted Benzo‐ and Naphthodithiophenes as Precursors for the Synthesis of Transient Open‐Shell Quinoids.” <i>ChemistryOpen</i> 12, no. 11 (2023). <a href=\"https://doi.org/10.1002/open.202300003\">https://doi.org/10.1002/open.202300003</a>.","apa":"Hou, P., Peschtrich, S., Feuerstein, W., Schoch, R., Hohloch, S., Breher, F., &#38; Paradies, J. (2023). Imidazolyl‐Substituted Benzo‐ and Naphthodithiophenes as Precursors for the Synthesis of Transient Open‐Shell Quinoids. <i>ChemistryOpen</i>, <i>12</i>(11), Article e202300003. <a href=\"https://doi.org/10.1002/open.202300003\">https://doi.org/10.1002/open.202300003</a>","short":"P. Hou, S. Peschtrich, W. Feuerstein, R. Schoch, S. Hohloch, F. Breher, J. Paradies, ChemistryOpen 12 (2023).","mla":"Hou, Peng, et al. “Imidazolyl‐Substituted Benzo‐ and Naphthodithiophenes as Precursors for the Synthesis of Transient Open‐Shell Quinoids.” <i>ChemistryOpen</i>, vol. 12, no. 11, e202300003, Wiley, 2023, doi:<a href=\"https://doi.org/10.1002/open.202300003\">10.1002/open.202300003</a>.","bibtex":"@article{Hou_Peschtrich_Feuerstein_Schoch_Hohloch_Breher_Paradies_2023, title={Imidazolyl‐Substituted Benzo‐ and Naphthodithiophenes as Precursors for the Synthesis of Transient Open‐Shell Quinoids}, volume={12}, DOI={<a href=\"https://doi.org/10.1002/open.202300003\">10.1002/open.202300003</a>}, number={11e202300003}, journal={ChemistryOpen}, publisher={Wiley}, author={Hou, Peng and Peschtrich, Sebastian and Feuerstein, Wolfram and Schoch, Roland and Hohloch, Stephan and Breher, Frank and Paradies, Jan}, year={2023} }"},"year":"2023","issue":"11","publication_identifier":{"issn":["2191-1363","2191-1363"]},"publication_status":"published","doi":"10.1002/open.202300003","title":"Imidazolyl‐Substituted Benzo‐ and Naphthodithiophenes as Precursors for the Synthesis of Transient Open‐Shell Quinoids","volume":12,"date_created":"2026-03-11T10:21:31Z","author":[{"first_name":"Peng","last_name":"Hou","full_name":"Hou, Peng"},{"last_name":"Peschtrich","full_name":"Peschtrich, Sebastian","first_name":"Sebastian"},{"first_name":"Wolfram","full_name":"Feuerstein, Wolfram","last_name":"Feuerstein"},{"full_name":"Schoch, Roland","last_name":"Schoch","first_name":"Roland"},{"first_name":"Stephan","full_name":"Hohloch, Stephan","last_name":"Hohloch"},{"first_name":"Frank","last_name":"Breher","full_name":"Breher, Frank"},{"full_name":"Paradies, Jan","id":"53339","orcid":"0000-0002-3698-668X","last_name":"Paradies","first_name":"Jan"}],"publisher":"Wiley","date_updated":"2026-03-11T10:21:47Z"},{"volume":28,"date_created":"2023-01-10T09:10:15Z","author":[{"first_name":"Peng","last_name":"Hou","full_name":"Hou, Peng"},{"first_name":"Sebastian","full_name":"Peschtrich, Sebastian","last_name":"Peschtrich"},{"first_name":"Nils","full_name":"Huber, Nils","last_name":"Huber"},{"last_name":"Feuerstein","full_name":"Feuerstein, Wolfram","first_name":"Wolfram"},{"full_name":"Bihlmeier, Angela","last_name":"Bihlmeier","first_name":"Angela"},{"first_name":"Ivo","last_name":"Krummenacher","full_name":"Krummenacher, Ivo"},{"first_name":"Roland","full_name":"Schoch, Roland","last_name":"Schoch"},{"last_name":"Klopper","full_name":"Klopper, Wim","first_name":"Wim"},{"full_name":"Breher, Frank","last_name":"Breher","first_name":"Frank"},{"full_name":"Paradies, Jan","id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan"}],"publisher":"Wiley","date_updated":"2023-01-23T12:47:43Z","doi":"10.1002/chem.202200982","title":"Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022)","issue":"23","publication_identifier":{"issn":["0947-6539","1521-3765"]},"publication_status":"published","intvolume":"        28","citation":{"chicago":"Hou, Peng, Sebastian Peschtrich, Nils Huber, Wolfram Feuerstein, Angela Bihlmeier, Ivo Krummenacher, Roland Schoch, Wim Klopper, Frank Breher, and Jan Paradies. “Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022).” <i>Chemistry – A European Journal</i> 28, no. 23 (2022). <a href=\"https://doi.org/10.1002/chem.202200982\">https://doi.org/10.1002/chem.202200982</a>.","ieee":"P. Hou <i>et al.</i>, “Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022),” <i>Chemistry – A European Journal</i>, vol. 28, no. 23, 2022, doi: <a href=\"https://doi.org/10.1002/chem.202200982\">10.1002/chem.202200982</a>.","ama":"Hou P, Peschtrich S, Huber N, et al. Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022). <i>Chemistry – A European Journal</i>. 2022;28(23). doi:<a href=\"https://doi.org/10.1002/chem.202200982\">10.1002/chem.202200982</a>","bibtex":"@article{Hou_Peschtrich_Huber_Feuerstein_Bihlmeier_Krummenacher_Schoch_Klopper_Breher_Paradies_2022, title={Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022)}, volume={28}, DOI={<a href=\"https://doi.org/10.1002/chem.202200982\">10.1002/chem.202200982</a>}, number={23}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Hou, Peng and Peschtrich, Sebastian and Huber, Nils and Feuerstein, Wolfram and Bihlmeier, Angela and Krummenacher, Ivo and Schoch, Roland and Klopper, Wim and Breher, Frank and Paradies, Jan}, year={2022} }","short":"P. Hou, S. Peschtrich, N. Huber, W. Feuerstein, A. Bihlmeier, I. Krummenacher, R. Schoch, W. Klopper, F. Breher, J. Paradies, Chemistry – A European Journal 28 (2022).","mla":"Hou, Peng, et al. “Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022).” <i>Chemistry – A European Journal</i>, vol. 28, no. 23, Wiley, 2022, doi:<a href=\"https://doi.org/10.1002/chem.202200982\">10.1002/chem.202200982</a>.","apa":"Hou, P., Peschtrich, S., Huber, N., Feuerstein, W., Bihlmeier, A., Krummenacher, I., Schoch, R., Klopper, W., Breher, F., &#38; Paradies, J. (2022). Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022). <i>Chemistry – A European Journal</i>, <i>28</i>(23). <a href=\"https://doi.org/10.1002/chem.202200982\">https://doi.org/10.1002/chem.202200982</a>"},"year":"2022","department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339","_id":"35703","language":[{"iso":"eng"}],"keyword":["General Chemistry","Catalysis","Organic Chemistry"],"publication":"Chemistry – A European Journal","type":"journal_article","status":"public"},{"abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>A frustrated Lewis pair‐catalyzed hydroboration of aromatic and aliphatic nitriles was developed. The catalyst provides the primary amines in high yields of 77–99% with catalyst loading as low as 2 mol%. The reaction displays high functional group tolerance towards esters, amides, nitro groups and aliphatic halides. The addition of the diborylated amines to ethyl 3‐phenylpropiolate proceeds with Z‐selectivity with d.r. of &gt;99:1 in 77–90% yield over two steps. The reaction mechanism was investigated by control and computational experiments.</jats:p><jats:p><jats:boxed-text content-type=\"graphic\" position=\"anchor\"><jats:graphic xmlns:xlink=\"http://www.w3.org/1999/xlink\" mimetype=\"image/png\" position=\"anchor\" specific-use=\"enlarged-web-image\" xlink:href=\"graphic/adsc202200525-toc-0001-m.png\"><jats:alt-text>magnified image</jats:alt-text></jats:graphic></jats:boxed-text>\r\n</jats:p>","lang":"eng"}],"publication":"Advanced Synthesis &amp; Catalysis","keyword":["hydroboration","nitrile","amine","frustrated Lewis pair","density functional theory"],"language":[{"iso":"eng"}],"year":"2022","quality_controlled":"1","issue":"18","title":"Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis","publisher":"Wiley","date_created":"2025-04-22T06:01:56Z","status":"public","type":"journal_article","_id":"59619","user_id":"62844","department":[{"_id":"389"}],"citation":{"ama":"Sieland B, Hoppe A, Stepen AJ, Paradies J. Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis. <i>Advanced Synthesis &#38;amp; Catalysis</i>. 2022;364(18):3143-3148. doi:<a href=\"https://doi.org/10.1002/adsc.202200525\">10.1002/adsc.202200525</a>","chicago":"Sieland, Benedikt, Axel Hoppe, Arne J. Stepen, and Jan Paradies. “Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis.” <i>Advanced Synthesis &#38;amp; Catalysis</i> 364, no. 18 (2022): 3143–48. <a href=\"https://doi.org/10.1002/adsc.202200525\">https://doi.org/10.1002/adsc.202200525</a>.","ieee":"B. Sieland, A. Hoppe, A. J. Stepen, and J. Paradies, “Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis,” <i>Advanced Synthesis &#38;amp; Catalysis</i>, vol. 364, no. 18, pp. 3143–3148, 2022, doi: <a href=\"https://doi.org/10.1002/adsc.202200525\">10.1002/adsc.202200525</a>.","apa":"Sieland, B., Hoppe, A., Stepen, A. J., &#38; Paradies, J. (2022). Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis. <i>Advanced Synthesis &#38;amp; Catalysis</i>, <i>364</i>(18), 3143–3148. <a href=\"https://doi.org/10.1002/adsc.202200525\">https://doi.org/10.1002/adsc.202200525</a>","mla":"Sieland, Benedikt, et al. “Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis.” <i>Advanced Synthesis &#38;amp; Catalysis</i>, vol. 364, no. 18, Wiley, 2022, pp. 3143–48, doi:<a href=\"https://doi.org/10.1002/adsc.202200525\">10.1002/adsc.202200525</a>.","short":"B. Sieland, A. Hoppe, A.J. Stepen, J. Paradies, Advanced Synthesis &#38;amp; Catalysis 364 (2022) 3143–3148.","bibtex":"@article{Sieland_Hoppe_Stepen_Paradies_2022, title={Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis}, volume={364}, DOI={<a href=\"https://doi.org/10.1002/adsc.202200525\">10.1002/adsc.202200525</a>}, number={18}, journal={Advanced Synthesis &#38;amp; Catalysis}, publisher={Wiley}, author={Sieland, Benedikt and Hoppe, Axel and Stepen, Arne J. and Paradies, Jan}, year={2022}, pages={3143–3148} }"},"intvolume":"       364","page":"3143-3148","publication_status":"published","publication_identifier":{"issn":["1615-4150","1615-4169"]},"main_file_link":[{"url":"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adsc.202200525","open_access":"1"}],"doi":"10.1002/adsc.202200525","oa":"1","date_updated":"2025-04-22T06:12:05Z","author":[{"first_name":"Benedikt","full_name":"Sieland, Benedikt","last_name":"Sieland"},{"last_name":"Hoppe","full_name":"Hoppe, Axel","id":"62844","first_name":"Axel"},{"full_name":"Stepen, Arne J.","last_name":"Stepen","first_name":"Arne J."},{"first_name":"Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X","id":"53339","full_name":"Paradies, Jan"}],"volume":364},{"doi":"10.1002/nadc.20214105947","title":"Organische Chemie","date_created":"2026-03-11T10:23:15Z","author":[{"full_name":"Paradies, Jan","id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan"},{"first_name":"Jennifer","full_name":"Andexer, Jennifer","last_name":"Andexer"},{"last_name":"Beifuss","full_name":"Beifuss, Uwe","first_name":"Uwe"},{"last_name":"Beuerle","full_name":"Beuerle, Florian","first_name":"Florian"},{"last_name":"Brasholz","full_name":"Brasholz, Malte","first_name":"Malte"},{"full_name":"Breinbauer, Rolf","last_name":"Breinbauer","first_name":"Rolf"},{"first_name":"Martin","last_name":"Ernst","full_name":"Ernst, Martin"},{"first_name":"Ruth","last_name":"Ganardi","full_name":"Ganardi, Ruth"},{"first_name":"Tobias A. M.","last_name":"Gulder","full_name":"Gulder, Tobias A. 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