--- _id: '64887' abstract: - lang: eng text: "Abstract\r\n 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." author: - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X citation: ama: Paradies J. Nichts zu lachen – oder doch? Nachrichten aus der Chemie. 2026;74(1):61-63. doi:10.1002/nadc.20264154740 apa: Paradies, J. (2026). Nichts zu lachen – oder doch? Nachrichten Aus Der Chemie, 74(1), 61–63. https://doi.org/10.1002/nadc.20264154740 bibtex: '@article{Paradies_2026, title={Nichts zu lachen – oder doch?}, volume={74}, DOI={10.1002/nadc.20264154740}, number={1}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Paradies, Jan}, year={2026}, pages={61–63} }' chicago: 'Paradies, Jan. “Nichts Zu Lachen – Oder Doch?” Nachrichten Aus Der Chemie 74, no. 1 (2026): 61–63. https://doi.org/10.1002/nadc.20264154740.' ieee: 'J. Paradies, “Nichts zu lachen – oder doch?,” Nachrichten aus der Chemie, vol. 74, no. 1, pp. 61–63, 2026, doi: 10.1002/nadc.20264154740.' mla: Paradies, Jan. “Nichts Zu Lachen – Oder Doch?” Nachrichten Aus Der Chemie, vol. 74, no. 1, Wiley, 2026, pp. 61–63, doi:10.1002/nadc.20264154740. short: J. Paradies, Nachrichten Aus Der Chemie 74 (2026) 61–63. date_created: 2026-03-11T10:14:54Z date_updated: 2026-03-11T10:15:07Z department: - _id: '2' - _id: '389' doi: 10.1002/nadc.20264154740 intvolume: ' 74' issue: '1' language: - iso: eng page: 61-63 publication: Nachrichten aus der Chemie publication_identifier: issn: - 1439-9598 - 1868-0054 publication_status: published publisher: Wiley status: public title: Nichts zu lachen – oder doch? type: journal_article user_id: '53339' volume: 74 year: '2026' ... --- _id: '64886' abstract: - lang: eng text: "\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 ortho\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 " article_number: e70158 author: - first_name: Jordan full_name: Berreur, Jordan last_name: Berreur - first_name: Julien full_name: Bortoluzzi, Julien last_name: Bortoluzzi - first_name: Laura full_name: Köring, Laura last_name: Köring - first_name: Frédéric R. full_name: Leroux, Frédéric R. last_name: Leroux - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X - first_name: Armen full_name: Panossian, Armen last_name: Panossian citation: ama: Berreur J, Bortoluzzi J, Köring L, Leroux FR, Paradies J, Panossian A. Double Functionalization of Atropisomeric Biphenyl Sulfoxides by Ortho ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids. European Journal of Inorganic Chemistry. Published online 2026. doi:10.1002/ejic.70158 apa: Berreur, J., Bortoluzzi, J., Köring, L., Leroux, F. R., Paradies, J., & Panossian, A. (2026). Double Functionalization of Atropisomeric Biphenyl Sulfoxides by Ortho ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids. European Journal of Inorganic Chemistry, Article e70158. https://doi.org/10.1002/ejic.70158 bibtex: '@article{Berreur_Bortoluzzi_Köring_Leroux_Paradies_Panossian_2026, title={Double Functionalization of Atropisomeric Biphenyl Sulfoxides by Ortho ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids}, DOI={10.1002/ejic.70158}, 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} }' chicago: Berreur, Jordan, Julien Bortoluzzi, Laura Köring, Frédéric R. Leroux, Jan Paradies, and Armen Panossian. “Double Functionalization of Atropisomeric Biphenyl Sulfoxides by Ortho ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids.” European Journal of Inorganic Chemistry, 2026. https://doi.org/10.1002/ejic.70158. ieee: 'J. Berreur, J. Bortoluzzi, L. Köring, F. R. Leroux, J. Paradies, and A. Panossian, “Double Functionalization of Atropisomeric Biphenyl Sulfoxides by Ortho ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids,” European Journal of Inorganic Chemistry, Art. no. e70158, 2026, doi: 10.1002/ejic.70158.' mla: Berreur, Jordan, et al. “Double Functionalization of Atropisomeric Biphenyl Sulfoxides by Ortho ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids.” European Journal of Inorganic Chemistry, e70158, Wiley, 2026, doi:10.1002/ejic.70158. short: J. Berreur, J. Bortoluzzi, L. Köring, F.R. Leroux, J. Paradies, A. Panossian, European Journal of Inorganic Chemistry (2026). date_created: 2026-03-11T10:10:08Z date_updated: 2026-03-11T10:36:31Z department: - _id: '2' - _id: '389' doi: 10.1002/ejic.70158 language: - iso: eng publication: European Journal of Inorganic Chemistry publication_identifier: issn: - 1434-1948 - 1099-0682 publication_status: published publisher: Wiley quality_controlled: '1' status: public title: Double Functionalization of Atropisomeric Biphenyl Sulfoxides by Ortho ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids type: journal_article user_id: '53339' year: '2026' ... --- _id: '61335' abstract: - lang: eng text: 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 PIII/PVO redox catalysis. This two‐step, one‐pot approach involves the activation of amides via PIII/PV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. article_number: '202500394' author: - first_name: Viktorija full_name: Medvaric, Viktorija id: '92677' last_name: Medvaric - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: 0000-0001-9025-3244 citation: 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. Advanced Synthesis and Catalysis. Published online 2025. doi:10.1002/adsc.70059 apa: Medvaric, V., Paradies, J., & Werner, T. (2025). Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides. Advanced Synthesis and Catalysis, Article 202500394. https://doi.org/10.1002/adsc.70059 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={10.1002/adsc.70059}, number={202500394}, journal={Advanced Synthesis and Catalysis}, publisher={Wiley}, author={Medvaric, Viktorija and Paradies, Jan and Werner, Thomas}, year={2025} }' 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.” Advanced Synthesis and Catalysis, 2025. https://doi.org/10.1002/adsc.70059. 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,” Advanced Synthesis and Catalysis, Art. no. 202500394, 2025, doi: 10.1002/adsc.70059.' mla: Medvaric, Viktorija, et al. “Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides.” Advanced Synthesis and Catalysis, 202500394, Wiley, 2025, doi:10.1002/adsc.70059. short: V. Medvaric, J. Paradies, T. Werner, Advanced Synthesis and Catalysis (2025). date_created: 2025-09-17T15:16:49Z date_updated: 2025-11-10T08:44:04Z department: - _id: '2' - _id: '389' doi: 10.1002/adsc.70059 keyword: - T2 - T - CSSD language: - iso: eng publication: Advanced Synthesis and Catalysis publication_identifier: issn: - 1615-4150 - 1615-4169 publication_status: published publisher: Wiley status: public title: Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides type: journal_article user_id: '89271' year: '2025' ... --- _id: '61336' article_number: jacs.5c06190 author: - first_name: Rundong full_name: Zhou, Rundong last_name: Zhou - first_name: Viktorija full_name: Medvaric, Viktorija id: '92677' last_name: Medvaric - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner orcid: https://orcid.org/0000-0001-9025-3244 - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X citation: ama: 'Zhou R, Medvaric V, Werner T, Paradies J. Metal-Free Reduction of Nitrous Oxide via P^III/P^V═O Cycling: Mechanistic Insights and Catalytic Performance. Journal of the American Chemical Society. Published online 2025. doi:10.1021/jacs.5c06190' apa: 'Zhou, R., Medvaric, V., Werner, T., & Paradies, J. (2025). Metal-Free Reduction of Nitrous Oxide via P^III/P^V═O Cycling: Mechanistic Insights and Catalytic Performance. Journal of the American Chemical Society, Article jacs. 5c06190. https://doi.org/10.1021/jacs.5c06190' bibtex: '@article{Zhou_Medvaric_Werner_Paradies_2025, title={Metal-Free Reduction of Nitrous Oxide via P^III/P^V═O Cycling: Mechanistic Insights and Catalytic Performance}, DOI={10.1021/jacs.5c06190}, 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} }' chicago: 'Zhou, Rundong, Viktorija Medvaric, Thomas Werner, and Jan Paradies. “Metal-Free Reduction of Nitrous Oxide via P^III/P^V═O Cycling: Mechanistic Insights and Catalytic Performance.” Journal of the American Chemical Society, 2025. https://doi.org/10.1021/jacs.5c06190.' ieee: 'R. Zhou, V. Medvaric, T. Werner, and J. Paradies, “Metal-Free Reduction of Nitrous Oxide via P^III/P^V═O Cycling: Mechanistic Insights and Catalytic Performance,” Journal of the American Chemical Society, Art. no. jacs. 5c06190, 2025, doi: 10.1021/jacs.5c06190.' mla: 'Zhou, Rundong, et al. “Metal-Free Reduction of Nitrous Oxide via P^III/P^V═O Cycling: Mechanistic Insights and Catalytic Performance.” Journal of the American Chemical Society, jacs. 5c06190, American Chemical Society (ACS), 2025, doi:10.1021/jacs.5c06190.' short: R. Zhou, V. Medvaric, T. Werner, J. Paradies, Journal of the American Chemical Society (2025). date_created: 2025-09-17T15:18:11Z date_updated: 2025-11-10T08:43:50Z department: - _id: '2' - _id: '389' doi: 10.1021/jacs.5c06190 keyword: - T2 - CSSD language: - iso: eng publication: Journal of the American Chemical Society publication_identifier: issn: - 0002-7863 - 1520-5126 publication_status: published publisher: American Chemical Society (ACS) status: public title: 'Metal-Free Reduction of Nitrous Oxide via P^III/P^V═O Cycling: Mechanistic Insights and Catalytic Performance' type: journal_article user_id: '89271' year: '2025' ... --- _id: '52541' abstract: - lang: eng text: AbstractWe 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 (DiPPF), as well as their tentative intermediates in the catalytic cycle. Reaction rates were measured and then compared to computational predictions. author: - first_name: Sebastian full_name: Peschtrich, Sebastian last_name: Peschtrich - first_name: Roland full_name: Schoch, Roland id: '48467' last_name: Schoch orcid: 0000-0003-2061-7289 - first_name: Dirk full_name: Kuckling, Dirk id: '287' last_name: Kuckling - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X 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. European Journal of Organic Chemistry. 2024;27(8). doi:10.1002/ejoc.202301207 apa: Peschtrich, S., Schoch, R., Kuckling, D., & 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. European Journal of Organic Chemistry, 27(8). https://doi.org/10.1002/ejoc.202301207 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={10.1002/ejoc.202301207}, number={8}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Peschtrich, Sebastian and Schoch, Roland and Kuckling, Dirk and Paradies, Jan}, year={2024} }' 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.” European Journal of Organic Chemistry 27, no. 8 (2024). https://doi.org/10.1002/ejoc.202301207. 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,” European Journal of Organic Chemistry, vol. 27, no. 8, 2024, doi: 10.1002/ejoc.202301207.' 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.” European Journal of Organic Chemistry, vol. 27, no. 8, Wiley, 2024, doi:10.1002/ejoc.202301207. short: S. Peschtrich, R. Schoch, D. Kuckling, J. Paradies, European Journal of Organic Chemistry 27 (2024). date_created: 2024-03-13T17:15:14Z date_updated: 2024-03-13T17:17:37Z department: - _id: '2' - _id: '389' doi: 10.1002/ejoc.202301207 intvolume: ' 27' issue: '8' keyword: - Organic Chemistry - Physical and Theoretical Chemistry language: - iso: eng publication: European Journal of Organic Chemistry publication_identifier: issn: - 1434-193X - 1099-0690 publication_status: published publisher: Wiley status: public title: A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes type: journal_article user_id: '53339' volume: 27 year: '2024' ... --- _id: '52572' abstract: - lang: eng text: 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. author: - first_name: Laura full_name: Köring, Laura last_name: Köring - first_name: Bernhard full_name: Birenheide, Bernhard last_name: Birenheide - first_name: Felix full_name: Krämer, Felix last_name: Krämer - first_name: Jonas O. full_name: Wenzel, Jonas O. last_name: Wenzel - first_name: Roland full_name: Schoch, Roland id: '48467' last_name: Schoch orcid: 0000-0003-2061-7289 - first_name: Martin full_name: Brehm, Martin id: '100167' last_name: Brehm - first_name: Frank full_name: Breher, Frank last_name: Breher - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X citation: ama: Köring L, Birenheide B, Krämer F, et al. Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements. European Journal of Inorganic Chemistry. Published online 2024. doi:10.1002/ejic.202400057 apa: Köring, L., Birenheide, B., Krämer, F., Wenzel, J. O., Schoch, R., Brehm, M., Breher, F., & Paradies, J. (2024). Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements. European Journal of Inorganic Chemistry. https://doi.org/10.1002/ejic.202400057 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={10.1002/ejic.202400057}, 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} }' 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.” European Journal of Inorganic Chemistry, 2024. https://doi.org/10.1002/ejic.202400057. ieee: 'L. Köring et al., “Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements,” European Journal of Inorganic Chemistry, 2024, doi: 10.1002/ejic.202400057.' mla: Köring, Laura, et al. “Synthesis of Ferrocenyl Boranes and Their Application as Lewis Acids in Epoxide Rearrangements.” European Journal of Inorganic Chemistry, Wiley, 2024, doi:10.1002/ejic.202400057. short: L. Köring, B. Birenheide, F. Krämer, J.O. Wenzel, R. Schoch, M. Brehm, F. Breher, J. Paradies, European Journal of Inorganic Chemistry (2024). date_created: 2024-03-14T07:09:09Z date_updated: 2024-03-14T07:10:37Z department: - _id: '2' - _id: '389' doi: 10.1002/ejic.202400057 keyword: - Inorganic Chemistry language: - iso: eng publication: European Journal of Inorganic Chemistry publication_identifier: issn: - 1434-1948 - 1099-0682 publication_status: published publisher: Wiley status: public title: Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements type: journal_article user_id: '53339' year: '2024' ... --- _id: '55371' abstract: - lang: eng text: AbstractThe activation of C(sp3)−F bonds by the commercially available catalyst B(C6F5)3 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). author: - first_name: Axel full_name: Hoppe, Axel last_name: Hoppe - first_name: Arne J. full_name: Stepen, Arne J. last_name: Stepen - first_name: Laura full_name: Köring, Laura last_name: Köring - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X citation: ama: Hoppe A, Stepen AJ, Köring L, Paradies J. Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds. Advanced Synthesis & Catalysis. 2024;366(13):2933-2938. doi:10.1002/adsc.202400511 apa: Hoppe, A., Stepen, A. J., Köring, L., & Paradies, J. (2024). Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds. Advanced Synthesis & Catalysis, 366(13), 2933–2938. https://doi.org/10.1002/adsc.202400511 bibtex: '@article{Hoppe_Stepen_Köring_Paradies_2024, title={Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds}, volume={366}, DOI={10.1002/adsc.202400511}, number={13}, journal={Advanced Synthesis & Catalysis}, publisher={Wiley}, author={Hoppe, Axel and Stepen, Arne J. and Köring, Laura and Paradies, Jan}, year={2024}, pages={2933–2938} }' chicago: 'Hoppe, Axel, Arne J. Stepen, Laura Köring, and Jan Paradies. “Tris(Pentafluorophenyl)Borane‐Catalyzed Functionalization of Benzylic C−F Bonds.” Advanced Synthesis & Catalysis 366, no. 13 (2024): 2933–38. https://doi.org/10.1002/adsc.202400511.' ieee: 'A. Hoppe, A. J. Stepen, L. Köring, and J. Paradies, “Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds,” Advanced Synthesis & Catalysis, vol. 366, no. 13, pp. 2933–2938, 2024, doi: 10.1002/adsc.202400511.' mla: Hoppe, Axel, et al. “Tris(Pentafluorophenyl)Borane‐Catalyzed Functionalization of Benzylic C−F Bonds.” Advanced Synthesis & Catalysis, vol. 366, no. 13, Wiley, 2024, pp. 2933–38, doi:10.1002/adsc.202400511. short: A. Hoppe, A.J. Stepen, L. Köring, J. Paradies, Advanced Synthesis & Catalysis 366 (2024) 2933–2938. date_created: 2024-07-24T09:16:15Z date_updated: 2024-07-24T09:18:18Z department: - _id: '2' - _id: '389' doi: 10.1002/adsc.202400511 intvolume: ' 366' issue: '13' language: - iso: eng page: 2933-2938 publication: Advanced Synthesis & Catalysis publication_identifier: issn: - 1615-4150 - 1615-4169 publication_status: published publisher: Wiley status: public title: Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds type: journal_article user_id: '53339' volume: 366 year: '2024' ... --- _id: '59616' abstract: - lang: eng text: AbstractThe activation of C(sp3)−F bonds by the commercially available catalyst B(C6F5)3 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). author: - first_name: Axel full_name: Hoppe, Axel id: '62844' last_name: Hoppe - first_name: Arne J. full_name: Stepen, Arne J. last_name: Stepen - first_name: Laura full_name: Köring, Laura last_name: Köring - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X citation: ama: Hoppe A, Stepen AJ, Köring L, Paradies J. Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds. Advanced Synthesis & Catalysis. 2024;366(13):2933-2938. doi:10.1002/adsc.202400511 apa: Hoppe, A., Stepen, A. J., Köring, L., & Paradies, J. (2024). Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds. Advanced Synthesis & Catalysis, 366(13), 2933–2938. https://doi.org/10.1002/adsc.202400511 bibtex: '@article{Hoppe_Stepen_Köring_Paradies_2024, title={Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds}, volume={366}, DOI={10.1002/adsc.202400511}, number={13}, journal={Advanced Synthesis & Catalysis}, publisher={Wiley}, author={Hoppe, Axel and Stepen, Arne J. and Köring, Laura and Paradies, Jan}, year={2024}, pages={2933–2938} }' chicago: 'Hoppe, Axel, Arne J. Stepen, Laura Köring, and Jan Paradies. “Tris(Pentafluorophenyl)Borane‐Catalyzed Functionalization of Benzylic C−F Bonds.” Advanced Synthesis & Catalysis 366, no. 13 (2024): 2933–38. https://doi.org/10.1002/adsc.202400511.' ieee: 'A. Hoppe, A. J. Stepen, L. Köring, and J. Paradies, “Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds,” Advanced Synthesis & Catalysis, vol. 366, no. 13, pp. 2933–2938, 2024, doi: 10.1002/adsc.202400511.' mla: Hoppe, Axel, et al. “Tris(Pentafluorophenyl)Borane‐Catalyzed Functionalization of Benzylic C−F Bonds.” Advanced Synthesis & Catalysis, vol. 366, no. 13, Wiley, 2024, pp. 2933–38, doi:10.1002/adsc.202400511. short: A. Hoppe, A.J. Stepen, L. Köring, J. Paradies, Advanced Synthesis & Catalysis 366 (2024) 2933–2938. date_created: 2025-04-22T05:59:08Z date_updated: 2025-04-22T06:11:59Z department: - _id: '389' doi: 10.1002/adsc.202400511 intvolume: ' 366' issue: '13' keyword: - fluoride - bond activation - borane - Lewis acid - C-C bond formation language: - iso: eng main_file_link: - open_access: '1' url: https://advanced.onlinelibrary.wiley.com/doi/10.1002/adsc.202400511 oa: '1' page: 2933-2938 publication: Advanced Synthesis & Catalysis publication_identifier: issn: - 1615-4150 - 1615-4169 publication_status: published publisher: Wiley quality_controlled: '1' status: public title: Tris(pentafluorophenyl)borane‐Catalyzed Functionalization of Benzylic C−F Bonds type: journal_article user_id: '62844' volume: 366 year: '2024' ... --- _id: '47589' author: - first_name: Felix full_name: Krämer, Felix last_name: Krämer - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X - first_name: Israel full_name: Fernández, Israel last_name: Fernández - first_name: Frank full_name: Breher, Frank last_name: Breher citation: 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. Nature Chemistry. Published online 2023. doi:10.1038/s41557-023-01340-9 apa: Krämer, F., Paradies, J., Fernández, I., & Breher, F. (2023). A crystalline aluminium–carbon-based ambiphile capable of activation and catalytic transfer of ammonia in non-aqueous media. Nature Chemistry. https://doi.org/10.1038/s41557-023-01340-9 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={10.1038/s41557-023-01340-9}, journal={Nature Chemistry}, publisher={Springer Science and Business Media LLC}, author={Krämer, Felix and Paradies, Jan and Fernández, Israel and Breher, Frank}, year={2023} }' 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.” Nature Chemistry, 2023. https://doi.org/10.1038/s41557-023-01340-9. 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,” Nature Chemistry, 2023, doi: 10.1038/s41557-023-01340-9.' mla: Krämer, Felix, et al. “A Crystalline Aluminium–Carbon-Based Ambiphile Capable of Activation and Catalytic Transfer of Ammonia in Non-Aqueous Media.” Nature Chemistry, Springer Science and Business Media LLC, 2023, doi:10.1038/s41557-023-01340-9. short: F. Krämer, J. Paradies, I. Fernández, F. Breher, Nature Chemistry (2023). date_created: 2023-10-04T14:40:07Z date_updated: 2023-10-04T14:41:12Z department: - _id: '2' - _id: '389' doi: 10.1038/s41557-023-01340-9 keyword: - General Chemical Engineering - General Chemistry language: - iso: eng publication: Nature Chemistry publication_identifier: issn: - 1755-4330 - 1755-4349 publication_status: published publisher: Springer Science and Business Media LLC status: public title: A crystalline aluminium–carbon-based ambiphile capable of activation and catalytic transfer of ammonia in non-aqueous media type: journal_article user_id: '53339' year: '2023' ... --- _id: '52542' abstract: - lang: eng text: 'AbstractWe report on so‐called “hidden FLPs” (FLP: frustrated Lewis pair) consisting of a phosphorus ylide featuring a group 13 fragment in the ortho 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 CO2 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.' author: - first_name: Felix full_name: Krämer, Felix last_name: Krämer - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X - first_name: Israel full_name: Fernández, Israel last_name: Fernández - first_name: Frank full_name: Breher, Frank last_name: Breher citation: ama: 'Krämer F, Paradies J, Fernández I, Breher F. Quo Vadis CO₂ Activation: Catalytic Reduction of CO₂ to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles. Chemistry – A European Journal. 2023;30(5). doi:10.1002/chem.202303380' apa: 'Krämer, F., Paradies, J., Fernández, I., & Breher, F. (2023). Quo Vadis CO₂ Activation: Catalytic Reduction of CO₂ to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles. Chemistry – A European Journal, 30(5). https://doi.org/10.1002/chem.202303380' bibtex: '@article{Krämer_Paradies_Fernández_Breher_2023, title={Quo Vadis CO₂ Activation: Catalytic Reduction of CO₂ to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles}, volume={30}, DOI={10.1002/chem.202303380}, number={5}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Krämer, Felix and Paradies, Jan and Fernández, Israel and Breher, Frank}, year={2023} }' chicago: 'Krämer, Felix, Jan Paradies, Israel Fernández, and Frank Breher. “Quo Vadis CO₂ Activation: Catalytic Reduction of CO₂ to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles.” Chemistry – A European Journal 30, no. 5 (2023). https://doi.org/10.1002/chem.202303380.' ieee: 'F. Krämer, J. Paradies, I. Fernández, and F. Breher, “Quo Vadis CO₂ Activation: Catalytic Reduction of CO₂ to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles,” Chemistry – A European Journal, vol. 30, no. 5, 2023, doi: 10.1002/chem.202303380.' mla: 'Krämer, Felix, et al. “Quo Vadis CO₂ Activation: Catalytic Reduction of CO₂ to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles.” Chemistry – A European Journal, vol. 30, no. 5, Wiley, 2023, doi:10.1002/chem.202303380.' short: F. Krämer, J. Paradies, I. Fernández, F. Breher, Chemistry – A European Journal 30 (2023). date_created: 2024-03-13T17:17:52Z date_updated: 2024-03-13T17:18:17Z department: - _id: '2' - _id: '389' doi: 10.1002/chem.202303380 intvolume: ' 30' issue: '5' keyword: - General Chemistry - Catalysis - Organic Chemistry language: - iso: eng publication: Chemistry – A European Journal publication_identifier: issn: - 0947-6539 - 1521-3765 publication_status: published publisher: Wiley status: public title: 'Quo Vadis CO₂ Activation: Catalytic Reduction of CO₂ to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles' type: journal_article user_id: '53339' volume: 30 year: '2023' ... --- _id: '42878' author: - first_name: Laura full_name: Köring, Laura last_name: Köring - first_name: Arne full_name: Stepen, Arne last_name: Stepen - first_name: Bernhard full_name: Birenheide, Bernhard last_name: Birenheide - first_name: Simon full_name: Barth, Simon last_name: Barth - first_name: Maxim full_name: Leskov, Maxim last_name: Leskov - first_name: Roland full_name: Schoch, Roland last_name: Schoch - first_name: Felix full_name: Krämer, Felix last_name: Krämer - first_name: Frank full_name: Breher, Frank last_name: Breher - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X 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. Angewandte Chemie International Edition. Published online 2023. doi:10.1002/anie.202301632' 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 International Edition. https://doi.org/10.1002/anie.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/anie.202301632}, 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} }' 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 International Edition, 2023. https://doi.org/10.1002/anie.202301632.' ieee: 'L. Köring et al., “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation,” Angewandte Chemie International Edition, 2023, doi: 10.1002/anie.202301632.' mla: 'Köring, Laura, et al. “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation.” Angewandte Chemie International Edition, Wiley, 2023, doi:10.1002/anie.202301632.' short: L. Köring, A. Stepen, B. Birenheide, S. Barth, M. Leskov, R. Schoch, F. Krämer, F. Breher, J. Paradies, Angewandte Chemie International Edition (2023). date_created: 2023-03-08T19:27:25Z date_updated: 2023-03-08T19:31:59Z department: - _id: '2' - _id: '389' doi: 10.1002/anie.202301632 keyword: - General Chemistry - Catalysis language: - iso: eng publication: Angewandte Chemie International Edition publication_identifier: issn: - 1433-7851 - 1521-3773 publication_status: published publisher: Wiley status: public title: 'Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation' type: journal_article user_id: '53339' year: '2023' ... --- _id: '42879' author: - first_name: Laura full_name: Köring, Laura last_name: Köring - first_name: Arne full_name: Stepen, Arne last_name: Stepen - first_name: Bernhard full_name: Birenheide, Bernhard last_name: Birenheide - first_name: Simon full_name: Barth, Simon last_name: Barth - first_name: Maxim full_name: Leskov, Maxim last_name: Leskov - first_name: Roland full_name: Schoch, Roland last_name: Schoch - first_name: Felix full_name: Krämer, Felix last_name: Krämer - first_name: Frank full_name: Breher, Frank last_name: Breher - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X 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. Angewandte Chemie. Published online 2023. doi:10.1002/ange.202301632' 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' 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} }' 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.' 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.' 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). date_created: 2023-03-08T19:31:03Z date_updated: 2023-03-08T19:32:09Z department: - _id: '2' - _id: '389' doi: 10.1002/ange.202301632 keyword: - General Medicine language: - iso: eng publication: Angewandte Chemie publication_identifier: issn: - 0044-8249 - 1521-3757 publication_status: published publisher: Wiley status: public title: 'Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation' type: journal_article user_id: '53339' year: '2023' ... --- _id: '44523' author: - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X citation: ama: Paradies J. Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations. Accounts of Chemical Research. 2023;56(7):821-834. doi:10.1021/acs.accounts.2c00832 apa: Paradies, J. (2023). Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations. Accounts of Chemical Research, 56(7), 821–834. https://doi.org/10.1021/acs.accounts.2c00832 bibtex: '@article{Paradies_2023, title={Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations}, volume={56}, DOI={10.1021/acs.accounts.2c00832}, number={7}, journal={Accounts of Chemical Research}, publisher={American Chemical Society (ACS)}, author={Paradies, Jan}, year={2023}, pages={821–834} }' chicago: 'Paradies, Jan. “Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations.” Accounts of Chemical Research 56, no. 7 (2023): 821–34. https://doi.org/10.1021/acs.accounts.2c00832.' ieee: 'J. Paradies, “Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations,” Accounts of Chemical Research, vol. 56, no. 7, pp. 821–834, 2023, doi: 10.1021/acs.accounts.2c00832.' mla: Paradies, Jan. “Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations.” Accounts of Chemical Research, vol. 56, no. 7, American Chemical Society (ACS), 2023, pp. 821–34, doi:10.1021/acs.accounts.2c00832. short: J. Paradies, Accounts of Chemical Research 56 (2023) 821–834. date_created: 2023-05-05T13:25:50Z date_updated: 2023-05-05T13:27:06Z department: - _id: '2' - _id: '389' doi: 10.1021/acs.accounts.2c00832 intvolume: ' 56' issue: '7' keyword: - General Medicine - General Chemistry language: - iso: eng page: 821-834 publication: Accounts of Chemical Research publication_identifier: issn: - 0001-4842 - 1520-4898 publication_status: published publisher: American Chemical Society (ACS) status: public title: Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations type: journal_article user_id: '53339' volume: 56 year: '2023' ... --- _id: '46277' author: - first_name: Benedikt full_name: Sieland, Benedikt last_name: Sieland - first_name: Marcel full_name: Stahn, Marcel last_name: Stahn - first_name: Roland full_name: Schoch, Roland last_name: Schoch - first_name: Constantin full_name: Daniliuc, Constantin last_name: Daniliuc - first_name: Sebastian full_name: Spicher, Sebastian last_name: Spicher - first_name: Stefan full_name: Grimme, Stefan last_name: Grimme - 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 citation: ama: Sieland B, Stahn M, Schoch R, et al. Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs. Angewandte Chemie International Edition. Published online 2023. doi:10.1002/anie.202308752 apa: Sieland, B., Stahn, M., Schoch, R., Daniliuc, C., Spicher, S., Grimme, S., Hansen, A., & Paradies, J. (2023). Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.202308752 bibtex: '@article{Sieland_Stahn_Schoch_Daniliuc_Spicher_Grimme_Hansen_Paradies_2023, title={Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs}, DOI={10.1002/anie.202308752}, 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} }' 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.” Angewandte Chemie International Edition, 2023. https://doi.org/10.1002/anie.202308752. ieee: 'B. Sieland et al., “Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs,” Angewandte Chemie International Edition, 2023, doi: 10.1002/anie.202308752.' mla: Sieland, Benedikt, et al. “Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs.” Angewandte Chemie International Edition, Wiley, 2023, doi:10.1002/anie.202308752. short: B. Sieland, M. Stahn, R. Schoch, C. Daniliuc, S. Spicher, S. Grimme, A. Hansen, J. Paradies, Angewandte Chemie International Edition (2023). date_created: 2023-08-03T09:00:33Z date_updated: 2023-08-03T09:01:41Z department: - _id: '2' - _id: '389' doi: 10.1002/anie.202308752 keyword: - General Chemistry - Catalysis language: - iso: eng publication: Angewandte Chemie International Edition publication_identifier: issn: - 1433-7851 - 1521-3773 publication_status: published publisher: Wiley status: public title: Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs type: journal_article user_id: '53339' year: '2023' ... --- _id: '64893' abstract: - lang: eng text: AbstractThe 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. article_number: e202300003 author: - first_name: Peng full_name: Hou, Peng last_name: Hou - first_name: Sebastian full_name: Peschtrich, Sebastian last_name: Peschtrich - first_name: Wolfram full_name: Feuerstein, Wolfram last_name: Feuerstein - first_name: Roland full_name: Schoch, Roland last_name: Schoch - first_name: Stephan full_name: Hohloch, Stephan last_name: Hohloch - first_name: Frank full_name: Breher, Frank last_name: Breher - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X 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. ChemistryOpen. 2023;12(11). doi:10.1002/open.202300003 apa: Hou, P., Peschtrich, S., Feuerstein, W., Schoch, R., Hohloch, S., Breher, F., & Paradies, J. (2023). Imidazolyl‐Substituted Benzo‐ and Naphthodithiophenes as Precursors for the Synthesis of Transient Open‐Shell Quinoids. ChemistryOpen, 12(11), Article e202300003. https://doi.org/10.1002/open.202300003 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={10.1002/open.202300003}, 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} }' 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.” ChemistryOpen 12, no. 11 (2023). https://doi.org/10.1002/open.202300003. ieee: 'P. Hou et al., “Imidazolyl‐Substituted Benzo‐ and Naphthodithiophenes as Precursors for the Synthesis of Transient Open‐Shell Quinoids,” ChemistryOpen, vol. 12, no. 11, Art. no. e202300003, 2023, doi: 10.1002/open.202300003.' mla: Hou, Peng, et al. “Imidazolyl‐Substituted Benzo‐ and Naphthodithiophenes as Precursors for the Synthesis of Transient Open‐Shell Quinoids.” ChemistryOpen, vol. 12, no. 11, e202300003, Wiley, 2023, doi:10.1002/open.202300003. short: P. Hou, S. Peschtrich, W. Feuerstein, R. Schoch, S. Hohloch, F. Breher, J. Paradies, ChemistryOpen 12 (2023). date_created: 2026-03-11T10:21:31Z date_updated: 2026-03-11T10:21:47Z department: - _id: '2' - _id: '389' doi: 10.1002/open.202300003 intvolume: ' 12' issue: '11' language: - iso: eng publication: ChemistryOpen publication_identifier: issn: - 2191-1363 - 2191-1363 publication_status: published publisher: Wiley status: public title: Imidazolyl‐Substituted Benzo‐ and Naphthodithiophenes as Precursors for the Synthesis of Transient Open‐Shell Quinoids type: journal_article user_id: '53339' volume: 12 year: '2023' ... --- _id: '35703' author: - first_name: Peng full_name: Hou, Peng last_name: Hou - first_name: Sebastian full_name: Peschtrich, Sebastian last_name: Peschtrich - first_name: Nils full_name: Huber, Nils last_name: Huber - first_name: Wolfram full_name: Feuerstein, Wolfram last_name: Feuerstein - first_name: Angela full_name: Bihlmeier, Angela last_name: Bihlmeier - first_name: Ivo full_name: Krummenacher, Ivo last_name: Krummenacher - first_name: Roland full_name: Schoch, Roland last_name: Schoch - first_name: Wim full_name: Klopper, Wim last_name: Klopper - first_name: Frank full_name: Breher, Frank last_name: Breher - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X citation: 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). Chemistry – A European Journal. 2022;28(23). doi:10.1002/chem.202200982' apa: 'Hou, P., Peschtrich, S., Huber, N., Feuerstein, W., Bihlmeier, A., Krummenacher, I., Schoch, R., Klopper, W., Breher, F., & Paradies, J. (2022). Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022). Chemistry – A European Journal, 28(23). https://doi.org/10.1002/chem.202200982' 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={10.1002/chem.202200982}, 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} }' 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).” Chemistry – A European Journal 28, no. 23 (2022). https://doi.org/10.1002/chem.202200982.' ieee: 'P. Hou et al., “Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022),” Chemistry – A European Journal, vol. 28, no. 23, 2022, doi: 10.1002/chem.202200982.' mla: 'Hou, Peng, et al. “Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022).” Chemistry – A European Journal, vol. 28, no. 23, Wiley, 2022, doi:10.1002/chem.202200982.' 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). date_created: 2023-01-10T09:10:15Z date_updated: 2023-01-23T12:47:43Z department: - _id: '2' - _id: '389' doi: 10.1002/chem.202200982 intvolume: ' 28' issue: '23' keyword: - General Chemistry - Catalysis - Organic Chemistry language: - iso: eng publication: Chemistry – A European Journal publication_identifier: issn: - 0947-6539 - 1521-3765 publication_status: published publisher: Wiley status: public title: 'Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022)' type: journal_article user_id: '53339' volume: 28 year: '2022' ... --- _id: '59619' abstract: - lang: eng text: "AbstractA 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 >99:1 in 77–90% yield over two steps. The reaction mechanism was investigated by control and computational experiments.

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\r\n" author: - first_name: Benedikt full_name: Sieland, Benedikt last_name: Sieland - first_name: Axel full_name: Hoppe, Axel id: '62844' last_name: Hoppe - first_name: Arne J. full_name: Stepen, Arne J. last_name: Stepen - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X citation: ama: 'Sieland B, Hoppe A, Stepen AJ, Paradies J. Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis. Advanced Synthesis & Catalysis. 2022;364(18):3143-3148. doi:10.1002/adsc.202200525' apa: 'Sieland, B., Hoppe, A., Stepen, A. J., & Paradies, J. (2022). Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis. Advanced Synthesis & Catalysis, 364(18), 3143–3148. https://doi.org/10.1002/adsc.202200525' bibtex: '@article{Sieland_Hoppe_Stepen_Paradies_2022, title={Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis}, volume={364}, DOI={10.1002/adsc.202200525}, number={18}, journal={Advanced Synthesis & Catalysis}, publisher={Wiley}, author={Sieland, Benedikt and Hoppe, Axel and Stepen, Arne J. and Paradies, Jan}, year={2022}, pages={3143–3148} }' chicago: 'Sieland, Benedikt, Axel Hoppe, Arne J. Stepen, and Jan Paradies. “Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis.” Advanced Synthesis & Catalysis 364, no. 18 (2022): 3143–48. https://doi.org/10.1002/adsc.202200525.' ieee: 'B. Sieland, A. Hoppe, A. J. Stepen, and J. Paradies, “Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis,” Advanced Synthesis & Catalysis, vol. 364, no. 18, pp. 3143–3148, 2022, doi: 10.1002/adsc.202200525.' mla: 'Sieland, Benedikt, et al. “Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis.” Advanced Synthesis & Catalysis, vol. 364, no. 18, Wiley, 2022, pp. 3143–48, doi:10.1002/adsc.202200525.' short: B. Sieland, A. Hoppe, A.J. Stepen, J. Paradies, Advanced Synthesis & Catalysis 364 (2022) 3143–3148. date_created: 2025-04-22T06:01:56Z date_updated: 2025-04-22T06:12:05Z department: - _id: '389' doi: 10.1002/adsc.202200525 intvolume: ' 364' issue: '18' keyword: - hydroboration - nitrile - amine - frustrated Lewis pair - density functional theory language: - iso: eng main_file_link: - open_access: '1' url: https://advanced.onlinelibrary.wiley.com/doi/10.1002/adsc.202200525 oa: '1' page: 3143-3148 publication: Advanced Synthesis & Catalysis publication_identifier: issn: - 1615-4150 - 1615-4169 publication_status: published publisher: Wiley quality_controlled: '1' status: public title: 'Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis' type: journal_article user_id: '62844' volume: 364 year: '2022' ... --- _id: '64895' abstract: - lang: eng text: AbstractElektrochemische Synthese – Naturstoffe und deren Synthese – photokatalytische Redoxchemie – Farbstoffe – Nanostrukturen – Wirkstoffe – asymmetrische Katalyse und mehr. author: - first_name: Jan full_name: Paradies, Jan id: '53339' last_name: Paradies orcid: 0000-0002-3698-668X - first_name: Jennifer full_name: Andexer, Jennifer last_name: Andexer - 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: Martin full_name: Ernst, Martin last_name: Ernst - first_name: Ruth full_name: Ganardi, Ruth last_name: Ganardi - 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: Stephanie full_name: Kath‐Schorr, Stephanie last_name: Kath‐Schorr - first_name: Karsten full_name: Körber, Karsten last_name: Körber - first_name: Markus full_name: Kordes, Markus last_name: Kordes - 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: Christian full_name: Mück‐Lichtenfeld, Christian last_name: Mück‐Lichtenfeld - first_name: Claudia full_name: Muhle‐Goll, Claudia last_name: Muhle‐Goll - first_name: Jochen full_name: Niemeyer, Jochen last_name: Niemeyer - first_name: Roland full_name: Pfau, Roland last_name: Pfau - first_name: Jörg full_name: Pietruszka, Jörg last_name: Pietruszka - first_name: Johannes L. full_name: Röckl, Johannes L. last_name: Röckl - first_name: Norbert full_name: Schaschke, Norbert last_name: Schaschke - first_name: Mathias O. full_name: Senge, Mathias O. last_name: Senge - first_name: Bernd F. full_name: Straub, Bernd F. last_name: Straub - first_name: Siegfried R. full_name: Waldvogel, Siegfried R. last_name: Waldvogel - 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 full_name: Winter, Christian last_name: Winter citation: ama: Paradies J, Andexer J, Beifuss U, et al. Organische Chemie. Nachrichten aus der Chemie. 2021;69(3):38-68. doi:10.1002/nadc.20214105947 apa: Paradies, J., Andexer, J., Beifuss, U., Beuerle, F., Brasholz, M., Breinbauer, R., Ernst, M., Ganardi, R., Gulder, T. A. M., Hüttel, W., Kath‐Schorr, S., Körber, K., Kordes, M., Lehmann, M., Lindel, T., Luy, B., Mück‐Lichtenfeld, C., Muhle‐Goll, C., Niemeyer, J., … Winter, C. (2021). Organische Chemie. Nachrichten Aus Der Chemie, 69(3), 38–68. https://doi.org/10.1002/nadc.20214105947 bibtex: '@article{Paradies_Andexer_Beifuss_Beuerle_Brasholz_Breinbauer_Ernst_Ganardi_Gulder_Hüttel_et al._2021, title={Organische Chemie}, volume={69}, DOI={10.1002/nadc.20214105947}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Paradies, Jan and Andexer, Jennifer and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ernst, Martin and Ganardi, Ruth and Gulder, Tobias A. M. and Hüttel, Wolfgang and et al.}, year={2021}, pages={38–68} }' chicago: 'Paradies, Jan, Jennifer Andexer, Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, Martin Ernst, et al. “Organische Chemie.” Nachrichten Aus Der Chemie 69, no. 3 (2021): 38–68. https://doi.org/10.1002/nadc.20214105947.' ieee: 'J. Paradies et al., “Organische Chemie,” Nachrichten aus der Chemie, vol. 69, no. 3, pp. 38–68, 2021, doi: 10.1002/nadc.20214105947.' mla: Paradies, Jan, et al. “Organische Chemie.” Nachrichten Aus Der Chemie, vol. 69, no. 3, Wiley, 2021, pp. 38–68, doi:10.1002/nadc.20214105947. short: J. Paradies, J. Andexer, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, M. Ernst, R. Ganardi, T.A.M. Gulder, W. Hüttel, S. Kath‐Schorr, K. Körber, M. Kordes, M. Lehmann, T. Lindel, B. Luy, C. Mück‐Lichtenfeld, C. Muhle‐Goll, J. Niemeyer, R. Pfau, J. Pietruszka, J.L. Röckl, N. Schaschke, M.O. Senge, B.F. Straub, S.R. Waldvogel, T. Werner, D.B. Werz, C. Winter, Nachrichten Aus Der Chemie 69 (2021) 38–68. date_created: 2026-03-11T10:23:15Z date_updated: 2026-03-11T10:23:22Z department: - _id: '2' - _id: '389' doi: 10.1002/nadc.20214105947 intvolume: ' 69' issue: '3' language: - iso: eng page: 38-68 publication: Nachrichten aus der Chemie publication_identifier: issn: - 1439-9598 - 1868-0054 publication_status: published publisher: Wiley status: public title: Organische Chemie type: journal_article user_id: '53339' volume: 69 year: '2021' ... --- _id: '37956' author: - first_name: Jennifer N. full_name: Andexer, Jennifer N. last_name: Andexer - 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: Martin full_name: Ernst, Martin last_name: Ernst - first_name: Julian full_name: Greb, Julian last_name: Greb - first_name: Tobias full_name: Gulder, Tobias last_name: Gulder - first_name: Wolfgang full_name: Hüttel, Wolfgang last_name: Hüttel - first_name: Stephanie full_name: Kath‐Schorr, Stephanie last_name: Kath‐Schorr - first_name: Markus full_name: Kordes, Markus last_name: Kordes - 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: Christian full_name: Mück‐Lichtenfeld, Christian last_name: Mück‐Lichtenfeld - first_name: Claudia full_name: Muhle, Claudia last_name: Muhle - first_name: Arun full_name: Narine, Arun last_name: Narine - first_name: Jörg full_name: Niemeyer, Jörg last_name: Niemeyer - 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 full_name: Senge, Mathias last_name: Senge - first_name: Bernd F. full_name: Straub, Bernd F. last_name: Straub - 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 full_name: Winter, Christian last_name: Winter citation: ama: Andexer JN, Beifuss U, Beuerle F, et al. Organische Chemie. Nachrichten aus der Chemie. 2020;68(3):42-72. doi:10.1002/nadc.20204095515 apa: Andexer, J. N., Beifuss, U., Beuerle, F., Brasholz, M., Breinbauer, R., Ernst, M., Greb, J., Gulder, T., Hüttel, W., Kath‐Schorr, S., Kordes, M., Lehmann, M., Lindel, T., Luy, B., Mück‐Lichtenfeld, C., Muhle, C., Narine, A., Niemeyer, J., Paradies, J., … Winter, C. (2020). Organische Chemie. Nachrichten Aus Der Chemie, 68(3), 42–72. https://doi.org/10.1002/nadc.20204095515 bibtex: '@article{Andexer_Beifuss_Beuerle_Brasholz_Breinbauer_Ernst_Greb_Gulder_Hüttel_Kath‐Schorr_et al._2020, title={Organische Chemie}, volume={68}, DOI={10.1002/nadc.20204095515}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Andexer, Jennifer N. and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ernst, Martin and Greb, Julian and Gulder, Tobias and Hüttel, Wolfgang and Kath‐Schorr, Stephanie and et al.}, year={2020}, pages={42–72} }' chicago: 'Andexer, Jennifer N., Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, Martin Ernst, Julian Greb, et al. “Organische Chemie.” Nachrichten Aus Der Chemie 68, no. 3 (2020): 42–72. https://doi.org/10.1002/nadc.20204095515.' ieee: 'J. N. Andexer et al., “Organische Chemie,” Nachrichten aus der Chemie, vol. 68, no. 3, pp. 42–72, 2020, doi: 10.1002/nadc.20204095515.' mla: Andexer, Jennifer N., et al. “Organische Chemie.” Nachrichten Aus Der Chemie, vol. 68, no. 3, Wiley, 2020, pp. 42–72, doi:10.1002/nadc.20204095515. short: J.N. Andexer, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, M. Ernst, J. Greb, T. Gulder, W. Hüttel, S. Kath‐Schorr, M. Kordes, M. Lehmann, T. Lindel, B. Luy, C. Mück‐Lichtenfeld, C. Muhle, A. Narine, J. Niemeyer, J. Paradies, R. Pfau, J. Pietruszka, N. Schaschke, M. Senge, B.F. Straub, T. Werner, D.B. Werz, C. Winter, Nachrichten Aus Der Chemie 68 (2020) 42–72. date_created: 2023-01-22T20:40:48Z date_updated: 2025-11-10T08:13:43Z department: - _id: '35' - _id: '2' - _id: '657' - _id: '389' doi: 10.1002/nadc.20204095515 extern: '1' intvolume: ' 68' issue: '3' keyword: - General Chemical Engineering - General Chemistry language: - iso: eng page: 42-72 publication: Nachrichten aus der Chemie publication_identifier: issn: - 1439-9598 - 1868-0054 publication_status: published publisher: Wiley status: public title: Organische Chemie type: journal_article user_id: '89271' volume: 68 year: '2020' ... --- _id: '64896' abstract: - lang: eng text: AbstractLichtinduzierte Prozesse effizient nutzen – Catenane und neue Kohlenstoffallotrope – komplexe Naturstoffe, einfache Wirkstoffe – Enzyme, Proteine und mehr, zusammengestellt von 26 Autoren, koordiniert von Jan Paradies. author: - first_name: Jennifer N. full_name: Andexer, Jennifer N. last_name: Andexer - 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: Martin full_name: Ernst, Martin last_name: Ernst - first_name: Julian full_name: Greb, Julian last_name: Greb - first_name: Tobias full_name: Gulder, Tobias last_name: Gulder - first_name: Wolfgang full_name: Hüttel, Wolfgang last_name: Hüttel - first_name: Stephanie full_name: Kath‐Schorr, Stephanie last_name: Kath‐Schorr - first_name: Markus full_name: Kordes, Markus last_name: Kordes - 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: Christian full_name: Mück‐Lichtenfeld, Christian last_name: Mück‐Lichtenfeld - first_name: Claudia full_name: Muhle, Claudia last_name: Muhle - first_name: Arun full_name: Narine, Arun last_name: Narine - first_name: Jörg full_name: Niemeyer, Jörg last_name: Niemeyer - 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 full_name: Senge, Mathias last_name: Senge - first_name: Bernd F. full_name: Straub, Bernd F. last_name: Straub - 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 full_name: Winter, Christian last_name: Winter citation: ama: Andexer JN, Beifuss U, Beuerle F, et al. Organische Chemie. Nachrichten aus der Chemie. 2020;68(3):42-72. doi:10.1002/nadc.20204095515 apa: Andexer, J. N., Beifuss, U., Beuerle, F., Brasholz, M., Breinbauer, R., Ernst, M., Greb, J., Gulder, T., Hüttel, W., Kath‐Schorr, S., Kordes, M., Lehmann, M., Lindel, T., Luy, B., Mück‐Lichtenfeld, C., Muhle, C., Narine, A., Niemeyer, J., Paradies, J., … Winter, C. (2020). Organische Chemie. Nachrichten Aus Der Chemie, 68(3), 42–72. https://doi.org/10.1002/nadc.20204095515 bibtex: '@article{Andexer_Beifuss_Beuerle_Brasholz_Breinbauer_Ernst_Greb_Gulder_Hüttel_Kath‐Schorr_et al._2020, title={Organische Chemie}, volume={68}, DOI={10.1002/nadc.20204095515}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Andexer, Jennifer N. and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ernst, Martin and Greb, Julian and Gulder, Tobias and Hüttel, Wolfgang and Kath‐Schorr, Stephanie and et al.}, year={2020}, pages={42–72} }' chicago: 'Andexer, Jennifer N., Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, Martin Ernst, Julian Greb, et al. “Organische Chemie.” Nachrichten Aus Der Chemie 68, no. 3 (2020): 42–72. https://doi.org/10.1002/nadc.20204095515.' ieee: 'J. N. Andexer et al., “Organische Chemie,” Nachrichten aus der Chemie, vol. 68, no. 3, pp. 42–72, 2020, doi: 10.1002/nadc.20204095515.' mla: Andexer, Jennifer N., et al. “Organische Chemie.” Nachrichten Aus Der Chemie, vol. 68, no. 3, Wiley, 2020, pp. 42–72, doi:10.1002/nadc.20204095515. short: J.N. Andexer, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, M. Ernst, J. Greb, T. Gulder, W. Hüttel, S. Kath‐Schorr, M. Kordes, M. Lehmann, T. Lindel, B. Luy, C. Mück‐Lichtenfeld, C. Muhle, A. Narine, J. Niemeyer, J. Paradies, R. Pfau, J. Pietruszka, N. Schaschke, M. Senge, B.F. Straub, T. Werner, D.B. Werz, C. Winter, Nachrichten Aus Der Chemie 68 (2020) 42–72. date_created: 2026-03-11T10:23:53Z date_updated: 2026-03-11T10:24:07Z department: - _id: '2' - _id: '389' doi: 10.1002/nadc.20204095515 intvolume: ' 68' issue: '3' language: - iso: eng page: 42-72 publication: Nachrichten aus der Chemie publication_identifier: issn: - 1439-9598 - 1868-0054 publication_status: published publisher: Wiley status: public title: Organische Chemie type: journal_article user_id: '53339' volume: 68 year: '2020' ...