[{"user_id":"53339","_id":"35691","language":[{"iso":"eng"}],"keyword":["General Chemistry","Catalysis"],"type":"journal_article","publication":"Angewandte Chemie International Edition","status":"public","author":[{"full_name":"Wicker, Garrit","last_name":"Wicker","first_name":"Garrit"},{"full_name":"Zhou, Rundong","last_name":"Zhou","first_name":"Rundong"},{"full_name":"Schoch, Roland","last_name":"Schoch","first_name":"Roland"},{"first_name":"Jan","id":"53339","full_name":"Paradies, Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X"}],"date_created":"2023-01-10T08:58:28Z","volume":61,"date_updated":"2023-01-23T12:51:42Z","publisher":"Wiley","doi":"10.1002/anie.202207944","title":"Cover Picture: Sigmatropic [1,5] Carbon Shift of Transient C3 Ammonium Enolates (Angew. Chem. Int. Ed. 31/2022)","issue":"31","publication_status":"published","publication_identifier":{"issn":["1433-7851","1521-3773"]},"citation":{"ama":"Wicker G, Zhou R, Schoch R, Paradies J. Cover Picture: Sigmatropic [1,5] Carbon Shift of Transient C3 Ammonium Enolates (Angew. Chem. Int. Ed. 31/2022). <i>Angewandte Chemie International Edition</i>. 2022;61(31). doi:<a href=\"https://doi.org/10.1002/anie.202207944\">10.1002/anie.202207944</a>","ieee":"G. Wicker, R. Zhou, R. Schoch, and J. Paradies, “Cover Picture: Sigmatropic [1,5] Carbon Shift of Transient C3 Ammonium Enolates (Angew. Chem. Int. Ed. 31/2022),” <i>Angewandte Chemie International Edition</i>, vol. 61, no. 31, 2022, doi: <a href=\"https://doi.org/10.1002/anie.202207944\">10.1002/anie.202207944</a>.","chicago":"Wicker, Garrit, Rundong Zhou, Roland Schoch, and Jan Paradies. “Cover Picture: Sigmatropic [1,5] Carbon Shift of Transient C3 Ammonium Enolates (Angew. Chem. Int. Ed. 31/2022).” <i>Angewandte Chemie International Edition</i> 61, no. 31 (2022). <a href=\"https://doi.org/10.1002/anie.202207944\">https://doi.org/10.1002/anie.202207944</a>.","short":"G. Wicker, R. Zhou, R. Schoch, J. Paradies, Angewandte Chemie International Edition 61 (2022).","mla":"Wicker, Garrit, et al. “Cover Picture: Sigmatropic [1,5] Carbon Shift of Transient C3 Ammonium Enolates (Angew. Chem. Int. Ed. 31/2022).” <i>Angewandte Chemie International Edition</i>, vol. 61, no. 31, Wiley, 2022, doi:<a href=\"https://doi.org/10.1002/anie.202207944\">10.1002/anie.202207944</a>.","bibtex":"@article{Wicker_Zhou_Schoch_Paradies_2022, title={Cover Picture: Sigmatropic [1,5] Carbon Shift of Transient C3 Ammonium Enolates (Angew. Chem. Int. Ed. 31/2022)}, volume={61}, DOI={<a href=\"https://doi.org/10.1002/anie.202207944\">10.1002/anie.202207944</a>}, number={31}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Wicker, Garrit and Zhou, Rundong and Schoch, Roland and Paradies, Jan}, year={2022} }","apa":"Wicker, G., Zhou, R., Schoch, R., &#38; Paradies, J. (2022). Cover Picture: Sigmatropic [1,5] Carbon Shift of Transient C3 Ammonium Enolates (Angew. Chem. Int. Ed. 31/2022). <i>Angewandte Chemie International Edition</i>, <i>61</i>(31). <a href=\"https://doi.org/10.1002/anie.202207944\">https://doi.org/10.1002/anie.202207944</a>"},"intvolume":"        61","year":"2022"},{"status":"public","type":"journal_article","publication":"Advanced Synthesis &amp; Catalysis","language":[{"iso":"eng"}],"keyword":["General Chemistry"],"user_id":"53339","_id":"35692","citation":{"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>","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} }","short":"B. Sieland, A. Hoppe, A.J. Stepen, J. Paradies, Advanced Synthesis &#38;amp; Catalysis 364 (2022) 3143–3148.","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>.","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>","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>.","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>."},"intvolume":"       364","page":"3143-3148","year":"2022","issue":"18","publication_status":"published","publication_identifier":{"issn":["1615-4150","1615-4169"]},"doi":"10.1002/adsc.202200525","title":"Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis","date_created":"2023-01-10T08:58:42Z","author":[{"first_name":"Benedikt","last_name":"Sieland","full_name":"Sieland, Benedikt"},{"first_name":"Axel","full_name":"Hoppe, Axel","last_name":"Hoppe"},{"first_name":"Arne J.","full_name":"Stepen, Arne J.","last_name":"Stepen"},{"first_name":"Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies","full_name":"Paradies, Jan","id":"53339"}],"volume":364,"date_updated":"2023-01-23T12:52:02Z","publisher":"Wiley"},{"type":"journal_article","status":"public","department":[{"_id":"389"}],"user_id":"62844","_id":"59619","publication_identifier":{"issn":["1615-4150","1615-4169"]},"publication_status":"published","intvolume":"       364","page":"3143-3148","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>.","short":"B. Sieland, A. Hoppe, A.J. Stepen, J. Paradies, Advanced Synthesis &#38;amp; Catalysis 364 (2022) 3143–3148.","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>.","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} }","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>"},"volume":364,"author":[{"full_name":"Sieland, Benedikt","last_name":"Sieland","first_name":"Benedikt"},{"first_name":"Axel","id":"62844","full_name":"Hoppe, Axel","last_name":"Hoppe"},{"first_name":"Arne J.","last_name":"Stepen","full_name":"Stepen, Arne J."},{"last_name":"Paradies","orcid":"0000-0002-3698-668X","id":"53339","full_name":"Paradies, Jan","first_name":"Jan"}],"date_updated":"2025-04-22T06:12:05Z","oa":"1","doi":"10.1002/adsc.202200525","main_file_link":[{"url":"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adsc.202200525","open_access":"1"}],"publication":"Advanced Synthesis &amp; Catalysis","abstract":[{"lang":"eng","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>"}],"language":[{"iso":"eng"}],"keyword":["hydroboration","nitrile","amine","frustrated Lewis pair","density functional theory"],"issue":"18","quality_controlled":"1","year":"2022","date_created":"2025-04-22T06:01:56Z","publisher":"Wiley","title":"Frustrated Lewis Pair‐Catalyzed Hydroboration of Nitriles: FLP Versus Borenium Catalysis"},{"issue":"46","year":"2021","publisher":"Royal Society of Chemistry (RSC)","date_created":"2022-05-03T06:48:33Z","title":"Coupling of CO<sub>2</sub> and epoxides catalysed by novel <i>N</i>-fused mesoionic carbene complexes of nickel(<scp>ii</scp>)","publication":"Dalton Transactions","keyword":["Inorganic Chemistry"],"language":[{"iso":"eng"}],"publication_status":"published","publication_identifier":{"issn":["1477-9226","1477-9234"]},"citation":{"chicago":"Watt, Fabian A., Benedikt Sieland, Nicole Dickmann, Roland Schoch, Regine Herbst-Irmer, Holger Ott, Jan Paradies, Dirk Kuckling, and Stephan Hohloch. “Coupling of CO<sub>2</sub> and Epoxides Catalysed by Novel <i>N</i>-Fused Mesoionic Carbene Complexes of Nickel(&#60;scp&#62;ii&#60;/Scp&#62;).” <i>Dalton Transactions</i> 50, no. 46 (2021): 17361–71. <a href=\"https://doi.org/10.1039/d1dt03311e\">https://doi.org/10.1039/d1dt03311e</a>.","ieee":"F. A. Watt <i>et al.</i>, “Coupling of CO<sub>2</sub> and epoxides catalysed by novel <i>N</i>-fused mesoionic carbene complexes of nickel(&#60;scp&#62;ii&#60;/scp&#62;),” <i>Dalton Transactions</i>, vol. 50, no. 46, pp. 17361–17371, 2021, doi: <a href=\"https://doi.org/10.1039/d1dt03311e\">10.1039/d1dt03311e</a>.","ama":"Watt FA, Sieland B, Dickmann N, et al. Coupling of CO<sub>2</sub> and epoxides catalysed by novel <i>N</i>-fused mesoionic carbene complexes of nickel(&#60;scp&#62;ii&#60;/scp&#62;). <i>Dalton Transactions</i>. 2021;50(46):17361-17371. doi:<a href=\"https://doi.org/10.1039/d1dt03311e\">10.1039/d1dt03311e</a>","apa":"Watt, F. A., Sieland, B., Dickmann, N., Schoch, R., Herbst-Irmer, R., Ott, H., Paradies, J., Kuckling, D., &#38; Hohloch, S. (2021). Coupling of CO<sub>2</sub> and epoxides catalysed by novel <i>N</i>-fused mesoionic carbene complexes of nickel(&#60;scp&#62;ii&#60;/scp&#62;). <i>Dalton Transactions</i>, <i>50</i>(46), 17361–17371. <a href=\"https://doi.org/10.1039/d1dt03311e\">https://doi.org/10.1039/d1dt03311e</a>","bibtex":"@article{Watt_Sieland_Dickmann_Schoch_Herbst-Irmer_Ott_Paradies_Kuckling_Hohloch_2021, title={Coupling of CO<sub>2</sub> and epoxides catalysed by novel <i>N</i>-fused mesoionic carbene complexes of nickel(&#60;scp&#62;ii&#60;/scp&#62;)}, volume={50}, DOI={<a href=\"https://doi.org/10.1039/d1dt03311e\">10.1039/d1dt03311e</a>}, number={46}, journal={Dalton Transactions}, publisher={Royal Society of Chemistry (RSC)}, author={Watt, Fabian A. and Sieland, Benedikt and Dickmann, Nicole and Schoch, Roland and Herbst-Irmer, Regine and Ott, Holger and Paradies, Jan and Kuckling, Dirk and Hohloch, Stephan}, year={2021}, pages={17361–17371} }","mla":"Watt, Fabian A., et al. “Coupling of CO<sub>2</sub> and Epoxides Catalysed by Novel <i>N</i>-Fused Mesoionic Carbene Complexes of Nickel(&#60;scp&#62;ii&#60;/Scp&#62;).” <i>Dalton Transactions</i>, vol. 50, no. 46, Royal Society of Chemistry (RSC), 2021, pp. 17361–71, doi:<a href=\"https://doi.org/10.1039/d1dt03311e\">10.1039/d1dt03311e</a>.","short":"F.A. Watt, B. Sieland, N. Dickmann, R. Schoch, R. Herbst-Irmer, H. Ott, J. Paradies, D. Kuckling, S. Hohloch, Dalton Transactions 50 (2021) 17361–17371."},"intvolume":"        50","page":"17361-17371","date_updated":"2022-07-28T10:03:45Z","author":[{"first_name":"Fabian A.","last_name":"Watt","full_name":"Watt, Fabian A."},{"first_name":"Benedikt","last_name":"Sieland","full_name":"Sieland, Benedikt"},{"first_name":"Nicole","full_name":"Dickmann, Nicole","last_name":"Dickmann"},{"full_name":"Schoch, Roland","last_name":"Schoch","first_name":"Roland"},{"first_name":"Regine","last_name":"Herbst-Irmer","full_name":"Herbst-Irmer, Regine"},{"first_name":"Holger","full_name":"Ott, Holger","last_name":"Ott"},{"orcid":"0000-0002-3698-668X","last_name":"Paradies","full_name":"Paradies, Jan","id":"53339","first_name":"Jan"},{"first_name":"Dirk","last_name":"Kuckling","id":"287","full_name":"Kuckling, Dirk"},{"first_name":"Stephan","full_name":"Hohloch, Stephan","last_name":"Hohloch"}],"volume":50,"doi":"10.1039/d1dt03311e","type":"journal_article","status":"public","_id":"31019","user_id":"94","department":[{"_id":"163"}]},{"title":"Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids","doi":"10.1002/anie.202103215","publisher":"Wiley","date_updated":"2022-12-09T12:19:12Z","author":[{"first_name":"Andrei","last_name":"Gurinov","full_name":"Gurinov, Andrei"},{"first_name":"Benedikt","last_name":"Sieland","full_name":"Sieland, Benedikt"},{"first_name":"Andrey","last_name":"Kuzhelev","full_name":"Kuzhelev, Andrey"},{"first_name":"Hossam","full_name":"Elgabarty, Hossam","id":"60250","last_name":"Elgabarty","orcid":"0000-0002-4945-1481"},{"first_name":"Thomas","id":"49079","full_name":"Kühne, Thomas","last_name":"Kühne"},{"first_name":"Thomas","full_name":"Prisner, Thomas","last_name":"Prisner"},{"first_name":"Jan","id":"53339","full_name":"Paradies, Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies"},{"first_name":"Marc","full_name":"Baldus, Marc","last_name":"Baldus"},{"last_name":"Ivanov","full_name":"Ivanov, Konstantin L.","first_name":"Konstantin L."},{"first_name":"Svetlana","id":"78888","full_name":"Pylaeva, Svetlana","last_name":"Pylaeva"}],"date_created":"2022-10-10T08:20:45Z","volume":60,"year":"2021","citation":{"ieee":"A. Gurinov <i>et al.</i>, “Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids,” <i>Angewandte Chemie International Edition</i>, vol. 60, no. 28, pp. 15371–15375, 2021, doi: <a href=\"https://doi.org/10.1002/anie.202103215\">10.1002/anie.202103215</a>.","chicago":"Gurinov, Andrei, Benedikt Sieland, Andrey Kuzhelev, Hossam Elgabarty, Thomas Kühne, Thomas Prisner, Jan Paradies, Marc Baldus, Konstantin L. Ivanov, and Svetlana Pylaeva. “Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids.” <i>Angewandte Chemie International Edition</i> 60, no. 28 (2021): 15371–75. <a href=\"https://doi.org/10.1002/anie.202103215\">https://doi.org/10.1002/anie.202103215</a>.","ama":"Gurinov A, Sieland B, Kuzhelev A, et al. Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids. <i>Angewandte Chemie International Edition</i>. 2021;60(28):15371-15375. doi:<a href=\"https://doi.org/10.1002/anie.202103215\">10.1002/anie.202103215</a>","mla":"Gurinov, Andrei, et al. “Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids.” <i>Angewandte Chemie International Edition</i>, vol. 60, no. 28, Wiley, 2021, pp. 15371–75, doi:<a href=\"https://doi.org/10.1002/anie.202103215\">10.1002/anie.202103215</a>.","bibtex":"@article{Gurinov_Sieland_Kuzhelev_Elgabarty_Kühne_Prisner_Paradies_Baldus_Ivanov_Pylaeva_2021, title={Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids}, volume={60}, DOI={<a href=\"https://doi.org/10.1002/anie.202103215\">10.1002/anie.202103215</a>}, number={28}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Gurinov, Andrei and Sieland, Benedikt and Kuzhelev, Andrey and Elgabarty, Hossam and Kühne, Thomas and Prisner, Thomas and Paradies, Jan and Baldus, Marc and Ivanov, Konstantin L. and Pylaeva, Svetlana}, year={2021}, pages={15371–15375} }","short":"A. Gurinov, B. Sieland, A. Kuzhelev, H. Elgabarty, T. Kühne, T. Prisner, J. Paradies, M. Baldus, K.L. Ivanov, S. Pylaeva, Angewandte Chemie International Edition 60 (2021) 15371–15375.","apa":"Gurinov, A., Sieland, B., Kuzhelev, A., Elgabarty, H., Kühne, T., Prisner, T., Paradies, J., Baldus, M., Ivanov, K. L., &#38; Pylaeva, S. (2021). Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids. <i>Angewandte Chemie International Edition</i>, <i>60</i>(28), 15371–15375. <a href=\"https://doi.org/10.1002/anie.202103215\">https://doi.org/10.1002/anie.202103215</a>"},"page":"15371-15375","intvolume":"        60","publication_status":"published","publication_identifier":{"issn":["1433-7851","1521-3773"]},"issue":"28","keyword":["General Chemistry","Catalysis"],"language":[{"iso":"eng"}],"_id":"33653","user_id":"60250","department":[{"_id":"613"}],"status":"public","type":"journal_article","publication":"Angewandte Chemie International Edition"},{"abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>The development of the frustrated Lewis pair catalyzed hydrogenation of tertiary and secondary amides is reviewed. Detailed insight into our strategies in order to overcome challenges during the reaction development process is provided. Furthermore, the developed chemistry is extended to the hydrogenation of polyamides and of trifluoroacetamides for the convenient introduction of trifluoroethyl groups into organic molecules.</jats:p>","lang":"eng"}],"status":"public","type":"journal_article","publication":"Synthesis","keyword":["Organic Chemistry","Catalysis"],"language":[{"iso":"eng"}],"_id":"35686","user_id":"53339","year":"2021","citation":{"apa":"Paradies, J., Köring, L., &#38; Sitte, N. A. (2021). Towards the Development of Frustrated Lewis Pair (FLP) Catalyzed Hydrogenations of Tertiary and Secondary Carboxylic Amides. <i>Synthesis</i>, <i>54</i>(05), 1287–1300. <a href=\"https://doi.org/10.1055/a-1681-3972\">https://doi.org/10.1055/a-1681-3972</a>","bibtex":"@article{Paradies_Köring_Sitte_2021, title={Towards the Development of Frustrated Lewis Pair (FLP) Catalyzed Hydrogenations of Tertiary and Secondary Carboxylic Amides}, volume={54}, DOI={<a href=\"https://doi.org/10.1055/a-1681-3972\">10.1055/a-1681-3972</a>}, number={05}, journal={Synthesis}, publisher={Georg Thieme Verlag KG}, author={Paradies, Jan and Köring, Laura and Sitte, Nikolai A.}, year={2021}, pages={1287–1300} }","mla":"Paradies, Jan, et al. “Towards the Development of Frustrated Lewis Pair (FLP) Catalyzed Hydrogenations of Tertiary and Secondary Carboxylic Amides.” <i>Synthesis</i>, vol. 54, no. 05, Georg Thieme Verlag KG, 2021, pp. 1287–300, doi:<a href=\"https://doi.org/10.1055/a-1681-3972\">10.1055/a-1681-3972</a>.","short":"J. Paradies, L. Köring, N.A. Sitte, Synthesis 54 (2021) 1287–1300.","ieee":"J. Paradies, L. Köring, and N. A. Sitte, “Towards the Development of Frustrated Lewis Pair (FLP) Catalyzed Hydrogenations of Tertiary and Secondary Carboxylic Amides,” <i>Synthesis</i>, vol. 54, no. 05, pp. 1287–1300, 2021, doi: <a href=\"https://doi.org/10.1055/a-1681-3972\">10.1055/a-1681-3972</a>.","chicago":"Paradies, Jan, Laura Köring, and Nikolai A. Sitte. “Towards the Development of Frustrated Lewis Pair (FLP) Catalyzed Hydrogenations of Tertiary and Secondary Carboxylic Amides.” <i>Synthesis</i> 54, no. 05 (2021): 1287–1300. <a href=\"https://doi.org/10.1055/a-1681-3972\">https://doi.org/10.1055/a-1681-3972</a>.","ama":"Paradies J, Köring L, Sitte NA. 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Organische Chemie. <i>Nachrichten aus der Chemie</i>. 2021;69(3):38-68. doi:<a href=\"https://doi.org/10.1002/nadc.20214105947\">10.1002/nadc.20214105947</a>","chicago":"Paradies, Jan, Jennifer Andexer, Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, Martin Ernst, et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i> 69, no. 3 (2021): 38–68. <a href=\"https://doi.org/10.1002/nadc.20214105947\">https://doi.org/10.1002/nadc.20214105947</a>.","ieee":"J. Paradies <i>et al.</i>, “Organische Chemie,” <i>Nachrichten aus der Chemie</i>, vol. 69, no. 3, pp. 38–68, 2021, doi: <a href=\"https://doi.org/10.1002/nadc.20214105947\">10.1002/nadc.20214105947</a>."},"intvolume":"        69","page":"38-68","year":"2021","user_id":"53339","department":[{"_id":"2"},{"_id":"389"}],"_id":"64895","language":[{"iso":"eng"}],"type":"journal_article","publication":"Nachrichten aus der Chemie","status":"public","abstract":[{"lang":"eng","text":"<jats:title>Abstract</jats:title><jats:p>Elektrochemische Synthese – Naturstoffe und deren Synthese – photokatalytische Redoxchemie – Farbstoffe – Nanostrukturen – Wirkstoffe – asymmetrische Katalyse und mehr.</jats:p>"}]},{"issue":"33","publication_identifier":{"issn":["1944-8244","1944-8252"]},"publication_status":"published","page":"36873-36881","intvolume":"        12","citation":{"chicago":"Li, Jie, Chendong Ji, Baozhong Lü, Maksim Rodin, Jan Paradies, Meizhen Yin, and Dirk Kuckling. “Dually Crosslinked Supramolecular Hydrogel for Cancer Biomarker Sensing.” <i>ACS Applied Materials &#38; Interfaces</i> 12, no. 33 (2020): 36873–81. <a href=\"https://doi.org/10.1021/acsami.0c08722\">https://doi.org/10.1021/acsami.0c08722</a>.","ieee":"J. Li <i>et al.</i>, “Dually Crosslinked Supramolecular Hydrogel for Cancer Biomarker Sensing,” <i>ACS Applied Materials &#38; Interfaces</i>, vol. 12, no. 33, pp. 36873–36881, 2020, doi: <a href=\"https://doi.org/10.1021/acsami.0c08722\">10.1021/acsami.0c08722</a>.","ama":"Li J, Ji C, Lü B, et al. Dually Crosslinked Supramolecular Hydrogel for Cancer Biomarker Sensing. <i>ACS Applied Materials &#38; Interfaces</i>. 2020;12(33):36873-36881. doi:<a href=\"https://doi.org/10.1021/acsami.0c08722\">10.1021/acsami.0c08722</a>","apa":"Li, J., Ji, C., Lü, B., Rodin, M., Paradies, J., Yin, M., &#38; Kuckling, D. (2020). 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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.","mla":"Andexer, Jennifer N., et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i>, vol. 68, no. 3, Wiley, 2020, pp. 42–72, doi:<a href=\"https://doi.org/10.1002/nadc.20204095515\">10.1002/nadc.20204095515</a>.","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. <i>Nachrichten Aus Der Chemie</i>, <i>68</i>(3), 42–72. <a href=\"https://doi.org/10.1002/nadc.20204095515\">https://doi.org/10.1002/nadc.20204095515</a>","ama":"Andexer JN, Beifuss U, Beuerle F, et al. Organische Chemie. <i>Nachrichten aus der Chemie</i>. 2020;68(3):42-72. doi:<a href=\"https://doi.org/10.1002/nadc.20204095515\">10.1002/nadc.20204095515</a>","chicago":"Andexer, Jennifer N., Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, Martin Ernst, Julian Greb, et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i> 68, no. 3 (2020): 42–72. <a href=\"https://doi.org/10.1002/nadc.20204095515\">https://doi.org/10.1002/nadc.20204095515</a>.","ieee":"J. N. Andexer <i>et al.</i>, “Organische Chemie,” <i>Nachrichten aus der Chemie</i>, vol. 68, no. 3, pp. 42–72, 2020, doi: <a href=\"https://doi.org/10.1002/nadc.20204095515\">10.1002/nadc.20204095515</a>."},"page":"42-72","intvolume":"        68","publisher":"Wiley","date_updated":"2026-03-11T10:24:07Z","author":[{"last_name":"Andexer","full_name":"Andexer, Jennifer N.","first_name":"Jennifer N."},{"first_name":"Uwe","full_name":"Beifuss, Uwe","last_name":"Beifuss"},{"first_name":"Florian","full_name":"Beuerle, Florian","last_name":"Beuerle"},{"last_name":"Brasholz","full_name":"Brasholz, Malte","first_name":"Malte"},{"last_name":"Breinbauer","full_name":"Breinbauer, Rolf","first_name":"Rolf"},{"last_name":"Ernst","full_name":"Ernst, Martin","first_name":"Martin"},{"first_name":"Julian","full_name":"Greb, Julian","last_name":"Greb"},{"last_name":"Gulder","full_name":"Gulder, Tobias","first_name":"Tobias"},{"full_name":"Hüttel, Wolfgang","last_name":"Hüttel","first_name":"Wolfgang"},{"full_name":"Kath‐Schorr, Stephanie","last_name":"Kath‐Schorr","first_name":"Stephanie"},{"first_name":"Markus","full_name":"Kordes, Markus","last_name":"Kordes"},{"first_name":"Matthias","full_name":"Lehmann, Matthias","last_name":"Lehmann"},{"last_name":"Lindel","full_name":"Lindel, Thomas","first_name":"Thomas"},{"full_name":"Luy, Burkhard","last_name":"Luy","first_name":"Burkhard"},{"full_name":"Mück‐Lichtenfeld, Christian","last_name":"Mück‐Lichtenfeld","first_name":"Christian"},{"full_name":"Muhle, Claudia","last_name":"Muhle","first_name":"Claudia"},{"first_name":"Arun","full_name":"Narine, Arun","last_name":"Narine"},{"first_name":"Jörg","last_name":"Niemeyer","full_name":"Niemeyer, Jörg"},{"full_name":"Paradies, Jan","id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan"},{"first_name":"Roland","full_name":"Pfau, Roland","last_name":"Pfau"},{"first_name":"Jörg","last_name":"Pietruszka","full_name":"Pietruszka, Jörg"},{"last_name":"Schaschke","full_name":"Schaschke, Norbert","first_name":"Norbert"},{"last_name":"Senge","full_name":"Senge, Mathias","first_name":"Mathias"},{"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.","last_name":"Werz","full_name":"Werz, Daniel B."},{"last_name":"Winter","full_name":"Winter, Christian","first_name":"Christian"}],"date_created":"2026-03-11T10:23:53Z","volume":68,"title":"Organische Chemie","doi":"10.1002/nadc.20204095515"},{"year":"2019","page":"5323-5326","citation":{"mla":"Deck, Eva, et al. “Redox-Responsive Phosphonite Gold Complexes in Hydroamination Catalysis.” <i>Chemical Communications</i>, 2019, pp. 5323–26, doi:<a href=\"https://doi.org/10.1039/c9cc01492f\">10.1039/c9cc01492f</a>.","short":"E. Deck, H.E. Wagner, J. Paradies, F. Breher, Chemical Communications (2019) 5323–5326.","bibtex":"@article{Deck_Wagner_Paradies_Breher_2019, title={Redox-responsive phosphonite gold complexes in hydroamination catalysis}, DOI={<a href=\"https://doi.org/10.1039/c9cc01492f\">10.1039/c9cc01492f</a>}, journal={Chemical Communications}, author={Deck, Eva and Wagner, Hanna E. and Paradies, Jan and Breher, Frank}, year={2019}, pages={5323–5326} }","apa":"Deck, E., Wagner, H. E., Paradies, J., &#38; Breher, F. (2019). Redox-responsive phosphonite gold complexes in hydroamination catalysis. <i>Chemical Communications</i>, 5323–5326. <a href=\"https://doi.org/10.1039/c9cc01492f\">https://doi.org/10.1039/c9cc01492f</a>","chicago":"Deck, Eva, Hanna E. Wagner, Jan Paradies, and Frank Breher. “Redox-Responsive Phosphonite Gold Complexes in Hydroamination Catalysis.” <i>Chemical Communications</i>, 2019, 5323–26. <a href=\"https://doi.org/10.1039/c9cc01492f\">https://doi.org/10.1039/c9cc01492f</a>.","ieee":"E. Deck, H. E. Wagner, J. Paradies, and F. Breher, “Redox-responsive phosphonite gold complexes in hydroamination catalysis,” <i>Chemical Communications</i>, pp. 5323–5326, 2019, doi: <a href=\"https://doi.org/10.1039/c9cc01492f\">10.1039/c9cc01492f</a>.","ama":"Deck E, Wagner HE, Paradies J, Breher F. Redox-responsive phosphonite gold complexes in hydroamination catalysis. <i>Chemical Communications</i>. 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