[{"publication_identifier":{"issn":["1615-4150"]},"publication_status":"published","page":"3656-3656","citation":{"ama":"Oechsle P, Hou P, Flörke U, Paradies J. Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016). <i>Advanced Synthesis &#38; Catalysis</i>. Published online 2016:3656-3656. doi:<a href=\"https://doi.org/10.1002/adsc.201601149\">10.1002/adsc.201601149</a>","chicago":"Oechsle, Peter, Peng Hou, Ulrich Flörke, and Jan Paradies. “Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016).” <i>Advanced Synthesis &#38; Catalysis</i>, 2016, 3656–3656. <a href=\"https://doi.org/10.1002/adsc.201601149\">https://doi.org/10.1002/adsc.201601149</a>.","ieee":"P. Oechsle, P. Hou, U. Flörke, and J. Paradies, “Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016),” <i>Advanced Synthesis &#38; Catalysis</i>, pp. 3656–3656, 2016, doi: <a href=\"https://doi.org/10.1002/adsc.201601149\">10.1002/adsc.201601149</a>.","apa":"Oechsle, P., Hou, P., Flörke, U., &#38; Paradies, J. (2016). Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016). <i>Advanced Synthesis &#38; Catalysis</i>, 3656–3656. <a href=\"https://doi.org/10.1002/adsc.201601149\">https://doi.org/10.1002/adsc.201601149</a>","mla":"Oechsle, Peter, et al. “Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016).” <i>Advanced Synthesis &#38; Catalysis</i>, 2016, pp. 3656–3656, doi:<a href=\"https://doi.org/10.1002/adsc.201601149\">10.1002/adsc.201601149</a>.","short":"P. Oechsle, P. Hou, U. Flörke, J. Paradies, Advanced Synthesis &#38; Catalysis (2016) 3656–3656.","bibtex":"@article{Oechsle_Hou_Flörke_Paradies_2016, title={Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016)}, DOI={<a href=\"https://doi.org/10.1002/adsc.201601149\">10.1002/adsc.201601149</a>}, journal={Advanced Synthesis &#38; Catalysis}, author={Oechsle, Peter and Hou, Peng and Flörke, Ulrich and Paradies, Jan}, year={2016}, pages={3656–3656} }"},"year":"2016","author":[{"last_name":"Oechsle","full_name":"Oechsle, Peter","first_name":"Peter"},{"first_name":"Peng","full_name":"Hou, Peng","last_name":"Hou"},{"last_name":"Flörke","full_name":"Flörke, Ulrich","first_name":"Ulrich"},{"first_name":"Jan","id":"53339","full_name":"Paradies, Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies"}],"date_created":"2021-05-26T10:51:41Z","date_updated":"2023-01-23T12:48:30Z","doi":"10.1002/adsc.201601149","title":"Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016)","publication":"Advanced Synthesis & Catalysis","type":"journal_article","status":"public","user_id":"53339","_id":"22254","language":[{"iso":"eng"}]},{"type":"journal_article","publication":"Angewandte Chemie International Edition","status":"public","_id":"22256","user_id":"53339","language":[{"iso":"eng"}],"publication_status":"published","publication_identifier":{"issn":["1433-7851"]},"year":"2016","citation":{"apa":"Maier, A. F. G., Tussing, S., Schneider, T., Flörke, U., Qu, Z.-W., Grimme, S., &#38; Paradies, J. (2016). Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles. <i>Angewandte Chemie International Edition</i>, 12219–12223. <a href=\"https://doi.org/10.1002/anie.201606426\">https://doi.org/10.1002/anie.201606426</a>","mla":"Maier, Alexander F. G., et al. “Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles.” <i>Angewandte Chemie International Edition</i>, 2016, pp. 12219–23, doi:<a href=\"https://doi.org/10.1002/anie.201606426\">10.1002/anie.201606426</a>.","short":"A.F.G. Maier, S. Tussing, T. Schneider, U. Flörke, Z.-W. Qu, S. Grimme, J. Paradies, Angewandte Chemie International Edition (2016) 12219–12223.","bibtex":"@article{Maier_Tussing_Schneider_Flörke_Qu_Grimme_Paradies_2016, title={Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles}, DOI={<a href=\"https://doi.org/10.1002/anie.201606426\">10.1002/anie.201606426</a>}, journal={Angewandte Chemie International Edition}, author={Maier, Alexander F. G. and Tussing, Sebastian and Schneider, Tobias and Flörke, Ulrich and Qu, Zheng-Wang and Grimme, Stefan and Paradies, Jan}, year={2016}, pages={12219–12223} }","ieee":"A. F. G. Maier <i>et al.</i>, “Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles,” <i>Angewandte Chemie International Edition</i>, pp. 12219–12223, 2016, doi: <a href=\"https://doi.org/10.1002/anie.201606426\">10.1002/anie.201606426</a>.","chicago":"Maier, Alexander F. G., Sebastian Tussing, Tobias Schneider, Ulrich Flörke, Zheng-Wang Qu, Stefan Grimme, and Jan Paradies. “Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles.” <i>Angewandte Chemie International Edition</i>, 2016, 12219–23. <a href=\"https://doi.org/10.1002/anie.201606426\">https://doi.org/10.1002/anie.201606426</a>.","ama":"Maier AFG, Tussing S, Schneider T, et al. Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles. <i>Angewandte Chemie International Edition</i>. Published online 2016:12219-12223. doi:<a href=\"https://doi.org/10.1002/anie.201606426\">10.1002/anie.201606426</a>"},"page":"12219-12223","date_updated":"2023-01-23T12:48:05Z","author":[{"full_name":"Maier, Alexander F. G.","last_name":"Maier","first_name":"Alexander F. G."},{"last_name":"Tussing","full_name":"Tussing, Sebastian","first_name":"Sebastian"},{"first_name":"Tobias","full_name":"Schneider, Tobias","last_name":"Schneider"},{"first_name":"Ulrich","last_name":"Flörke","full_name":"Flörke, Ulrich"},{"first_name":"Zheng-Wang","full_name":"Qu, Zheng-Wang","last_name":"Qu"},{"first_name":"Stefan","full_name":"Grimme, Stefan","last_name":"Grimme"},{"first_name":"Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X","full_name":"Paradies, Jan","id":"53339"}],"date_created":"2021-05-26T10:52:19Z","title":"Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles","doi":"10.1002/anie.201606426"},{"status":"public","type":"journal_article","publication":"Angewandte Chemie","language":[{"iso":"eng"}],"_id":"22255","user_id":"53339","year":"2016","citation":{"ama":"Maier AFG, Tussing S, Schneider T, et al. Dehydrierende Oxidation von Indolinen und anderen Heterocyclen durch frustrierte Lewis-Paare. <i>Angewandte Chemie</i>. Published online 2016:12407-12411. doi:<a href=\"https://doi.org/10.1002/ange.201606426\">10.1002/ange.201606426</a>","chicago":"Maier, Alexander F. G., Sebastian Tussing, Tobias Schneider, Ulrich Flörke, Zheng-Wang Qu, Stefan Grimme, and Jan Paradies. “Dehydrierende Oxidation von Indolinen Und Anderen Heterocyclen Durch Frustrierte Lewis-Paare.” <i>Angewandte Chemie</i>, 2016, 12407–11. <a href=\"https://doi.org/10.1002/ange.201606426\">https://doi.org/10.1002/ange.201606426</a>.","ieee":"A. F. G. Maier <i>et al.</i>, “Dehydrierende Oxidation von Indolinen und anderen Heterocyclen durch frustrierte Lewis-Paare,” <i>Angewandte Chemie</i>, pp. 12407–12411, 2016, doi: <a href=\"https://doi.org/10.1002/ange.201606426\">10.1002/ange.201606426</a>.","short":"A.F.G. Maier, S. Tussing, T. Schneider, U. Flörke, Z.-W. Qu, S. Grimme, J. Paradies, Angewandte Chemie (2016) 12407–12411.","bibtex":"@article{Maier_Tussing_Schneider_Flörke_Qu_Grimme_Paradies_2016, title={Dehydrierende Oxidation von Indolinen und anderen Heterocyclen durch frustrierte Lewis-Paare}, DOI={<a href=\"https://doi.org/10.1002/ange.201606426\">10.1002/ange.201606426</a>}, journal={Angewandte Chemie}, author={Maier, Alexander F. G. and Tussing, Sebastian and Schneider, Tobias and Flörke, Ulrich and Qu, Zheng-Wang and Grimme, Stefan and Paradies, Jan}, year={2016}, pages={12407–12411} }","mla":"Maier, Alexander F. G., et al. “Dehydrierende Oxidation von Indolinen Und Anderen Heterocyclen Durch Frustrierte Lewis-Paare.” <i>Angewandte Chemie</i>, 2016, pp. 12407–11, doi:<a href=\"https://doi.org/10.1002/ange.201606426\">10.1002/ange.201606426</a>.","apa":"Maier, A. F. G., Tussing, S., Schneider, T., Flörke, U., Qu, Z.-W., Grimme, S., &#38; Paradies, J. (2016). Dehydrierende Oxidation von Indolinen und anderen Heterocyclen durch frustrierte Lewis-Paare. <i>Angewandte Chemie</i>, 12407–12411. <a href=\"https://doi.org/10.1002/ange.201606426\">https://doi.org/10.1002/ange.201606426</a>"},"page":"12407-12411","publication_status":"published","publication_identifier":{"issn":["0044-8249"]},"title":"Dehydrierende Oxidation von Indolinen und anderen Heterocyclen durch frustrierte Lewis-Paare","doi":"10.1002/ange.201606426","date_updated":"2023-01-23T12:48:16Z","date_created":"2021-05-26T10:52:06Z","author":[{"last_name":"Maier","full_name":"Maier, Alexander F. G.","first_name":"Alexander F. G."},{"last_name":"Tussing","full_name":"Tussing, Sebastian","first_name":"Sebastian"},{"first_name":"Tobias","last_name":"Schneider","full_name":"Schneider, Tobias"},{"first_name":"Ulrich","full_name":"Flörke, Ulrich","last_name":"Flörke"},{"first_name":"Zheng-Wang","full_name":"Qu, Zheng-Wang","last_name":"Qu"},{"first_name":"Stefan","full_name":"Grimme, Stefan","last_name":"Grimme"},{"full_name":"Paradies, Jan","id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan"}]},{"language":[{"iso":"eng"}],"user_id":"53339","_id":"22252","status":"public","publication":"Angewandte Chemie International Edition","type":"journal_article","doi":"10.1002/anie.201511921","title":"Frustrated Lewis Pair-Catalyzed Cycloisomerization of 1,5-Enynes via a 5-endo-dig Cyclization/Protodeborylation Sequence","author":[{"first_name":"Sergej","last_name":"Tamke","full_name":"Tamke, Sergej"},{"last_name":"Qu","full_name":"Qu, Zheng-Wang","first_name":"Zheng-Wang"},{"first_name":"Nikolai A.","last_name":"Sitte","full_name":"Sitte, Nikolai A."},{"first_name":"Ulrich","last_name":"Flörke","full_name":"Flörke, Ulrich"},{"full_name":"Grimme, Stefan","last_name":"Grimme","first_name":"Stefan"},{"first_name":"Jan","id":"53339","full_name":"Paradies, Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X"}],"date_created":"2021-05-26T10:48:55Z","date_updated":"2023-01-23T12:48:50Z","page":"4336-4339","citation":{"short":"S. Tamke, Z.-W. Qu, N.A. Sitte, U. Flörke, S. Grimme, J. Paradies, Angewandte Chemie International Edition (2016) 4336–4339.","mla":"Tamke, Sergej, et al. “Frustrated Lewis Pair-Catalyzed Cycloisomerization of 1,5-Enynes via a 5-Endo-Dig Cyclization/Protodeborylation Sequence.” <i>Angewandte Chemie International Edition</i>, 2016, pp. 4336–39, doi:<a href=\"https://doi.org/10.1002/anie.201511921\">10.1002/anie.201511921</a>.","bibtex":"@article{Tamke_Qu_Sitte_Flörke_Grimme_Paradies_2016, title={Frustrated Lewis Pair-Catalyzed Cycloisomerization of 1,5-Enynes via a 5-endo-dig Cyclization/Protodeborylation Sequence}, DOI={<a href=\"https://doi.org/10.1002/anie.201511921\">10.1002/anie.201511921</a>}, journal={Angewandte Chemie International Edition}, author={Tamke, Sergej and Qu, Zheng-Wang and Sitte, Nikolai A. and Flörke, Ulrich and Grimme, Stefan and Paradies, Jan}, year={2016}, pages={4336–4339} }","apa":"Tamke, S., Qu, Z.-W., Sitte, N. A., Flörke, U., Grimme, S., &#38; Paradies, J. (2016). Frustrated Lewis Pair-Catalyzed Cycloisomerization of 1,5-Enynes via a 5-endo-dig Cyclization/Protodeborylation Sequence. <i>Angewandte Chemie International Edition</i>, 4336–4339. <a href=\"https://doi.org/10.1002/anie.201511921\">https://doi.org/10.1002/anie.201511921</a>","ama":"Tamke S, Qu Z-W, Sitte NA, Flörke U, Grimme S, Paradies J. Frustrated Lewis Pair-Catalyzed Cycloisomerization of 1,5-Enynes via a 5-endo-dig Cyclization/Protodeborylation Sequence. <i>Angewandte Chemie International Edition</i>. Published online 2016:4336-4339. doi:<a href=\"https://doi.org/10.1002/anie.201511921\">10.1002/anie.201511921</a>","ieee":"S. Tamke, Z.-W. Qu, N. A. Sitte, U. Flörke, S. Grimme, and J. Paradies, “Frustrated Lewis Pair-Catalyzed Cycloisomerization of 1,5-Enynes via a 5-endo-dig Cyclization/Protodeborylation Sequence,” <i>Angewandte Chemie International Edition</i>, pp. 4336–4339, 2016, doi: <a href=\"https://doi.org/10.1002/anie.201511921\">10.1002/anie.201511921</a>.","chicago":"Tamke, Sergej, Zheng-Wang Qu, Nikolai A. Sitte, Ulrich Flörke, Stefan Grimme, and Jan Paradies. “Frustrated Lewis Pair-Catalyzed Cycloisomerization of 1,5-Enynes via a 5-Endo-Dig Cyclization/Protodeborylation Sequence.” <i>Angewandte Chemie International Edition</i>, 2016, 4336–39. <a href=\"https://doi.org/10.1002/anie.201511921\">https://doi.org/10.1002/anie.201511921</a>."},"year":"2016","publication_identifier":{"issn":["1433-7851"]},"publication_status":"published"},{"status":"public","type":"journal_article","publication":"Angewandte Chemie International Edition","language":[{"iso":"eng"}],"_id":"22250","user_id":"53339","year":"2016","citation":{"mla":"Maier, Alexander F. G., et al. “Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles.” <i>Angewandte Chemie International Edition</i>, 2016, pp. 12219–23, doi:<a href=\"https://doi.org/10.1002/anie.201606426\">10.1002/anie.201606426</a>.","short":"A.F.G. Maier, S. Tussing, T. Schneider, U. Flörke, Z.-W. Qu, S. Grimme, J. Paradies, Angewandte Chemie International Edition (2016) 12219–12223.","bibtex":"@article{Maier_Tussing_Schneider_Flörke_Qu_Grimme_Paradies_2016, title={Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles}, DOI={<a href=\"https://doi.org/10.1002/anie.201606426\">10.1002/anie.201606426</a>}, journal={Angewandte Chemie International Edition}, author={Maier, Alexander F. G. and Tussing, Sebastian and Schneider, Tobias and Flörke, Ulrich and Qu, Zheng-Wang and Grimme, Stefan and Paradies, Jan}, year={2016}, pages={12219–12223} }","apa":"Maier, A. F. G., Tussing, S., Schneider, T., Flörke, U., Qu, Z.-W., Grimme, S., &#38; Paradies, J. (2016). Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles. <i>Angewandte Chemie International Edition</i>, 12219–12223. <a href=\"https://doi.org/10.1002/anie.201606426\">https://doi.org/10.1002/anie.201606426</a>","ama":"Maier AFG, Tussing S, Schneider T, et al. Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles. <i>Angewandte Chemie International Edition</i>. Published online 2016:12219-12223. doi:<a href=\"https://doi.org/10.1002/anie.201606426\">10.1002/anie.201606426</a>","ieee":"A. F. G. Maier <i>et al.</i>, “Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles,” <i>Angewandte Chemie International Edition</i>, pp. 12219–12223, 2016, doi: <a href=\"https://doi.org/10.1002/anie.201606426\">10.1002/anie.201606426</a>.","chicago":"Maier, Alexander F. G., Sebastian Tussing, Tobias Schneider, Ulrich Flörke, Zheng-Wang Qu, Stefan Grimme, and Jan Paradies. “Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles.” <i>Angewandte Chemie International Edition</i>, 2016, 12219–23. <a href=\"https://doi.org/10.1002/anie.201606426\">https://doi.org/10.1002/anie.201606426</a>."},"page":"12219-12223","publication_status":"published","publication_identifier":{"issn":["1433-7851"]},"title":"Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles","doi":"10.1002/anie.201606426","date_updated":"2023-01-23T12:49:13Z","date_created":"2021-05-26T10:47:40Z","author":[{"last_name":"Maier","full_name":"Maier, Alexander F. G.","first_name":"Alexander F. G."},{"first_name":"Sebastian","last_name":"Tussing","full_name":"Tussing, Sebastian"},{"last_name":"Schneider","full_name":"Schneider, Tobias","first_name":"Tobias"},{"first_name":"Ulrich","last_name":"Flörke","full_name":"Flörke, Ulrich"},{"first_name":"Zheng-Wang","last_name":"Qu","full_name":"Qu, Zheng-Wang"},{"full_name":"Grimme, Stefan","last_name":"Grimme","first_name":"Stefan"},{"last_name":"Paradies","orcid":"0000-0002-3698-668X","full_name":"Paradies, Jan","id":"53339","first_name":"Jan"}]},{"date_updated":"2023-01-23T12:49:30Z","author":[{"first_name":"Peter","last_name":"Oechsle","full_name":"Oechsle, Peter"},{"full_name":"Hou, Peng","last_name":"Hou","first_name":"Peng"},{"full_name":"Flörke, Ulrich","last_name":"Flörke","first_name":"Ulrich"},{"last_name":"Paradies","orcid":"0000-0002-3698-668X","id":"53339","full_name":"Paradies, Jan","first_name":"Jan"}],"date_created":"2021-05-26T10:44:59Z","title":"Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence","doi":"10.1002/adsc.201600802","publication_identifier":{"issn":["1615-4150"]},"publication_status":"published","year":"2016","page":"3770-3776","citation":{"short":"P. Oechsle, P. Hou, U. Flörke, J. Paradies, Advanced Synthesis &#38; Catalysis (2016) 3770–3776.","bibtex":"@article{Oechsle_Hou_Flörke_Paradies_2016, title={Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence}, DOI={<a href=\"https://doi.org/10.1002/adsc.201600802\">10.1002/adsc.201600802</a>}, journal={Advanced Synthesis &#38; Catalysis}, author={Oechsle, Peter and Hou, Peng and Flörke, Ulrich and Paradies, Jan}, year={2016}, pages={3770–3776} }","mla":"Oechsle, Peter, et al. “Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence.” <i>Advanced Synthesis &#38; Catalysis</i>, 2016, pp. 3770–76, doi:<a href=\"https://doi.org/10.1002/adsc.201600802\">10.1002/adsc.201600802</a>.","apa":"Oechsle, P., Hou, P., Flörke, U., &#38; Paradies, J. (2016). Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence. <i>Advanced Synthesis &#38; Catalysis</i>, 3770–3776. <a href=\"https://doi.org/10.1002/adsc.201600802\">https://doi.org/10.1002/adsc.201600802</a>","chicago":"Oechsle, Peter, Peng Hou, Ulrich Flörke, and Jan Paradies. “Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence.” <i>Advanced Synthesis &#38; Catalysis</i>, 2016, 3770–76. <a href=\"https://doi.org/10.1002/adsc.201600802\">https://doi.org/10.1002/adsc.201600802</a>.","ieee":"P. Oechsle, P. Hou, U. Flörke, and J. Paradies, “Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence,” <i>Advanced Synthesis &#38; Catalysis</i>, pp. 3770–3776, 2016, doi: <a href=\"https://doi.org/10.1002/adsc.201600802\">10.1002/adsc.201600802</a>.","ama":"Oechsle P, Hou P, Flörke U, Paradies J. Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence. <i>Advanced Synthesis &#38; Catalysis</i>. Published online 2016:3770-3776. doi:<a href=\"https://doi.org/10.1002/adsc.201600802\">10.1002/adsc.201600802</a>"},"_id":"22249","user_id":"53339","language":[{"iso":"eng"}],"publication":"Advanced Synthesis & Catalysis","type":"journal_article","status":"public"},{"language":[{"iso":"eng"}],"user_id":"53339","_id":"22251","status":"public","publication":"Chemistry - A European Journal","type":"journal_article","doi":"10.1002/chem.201600716","title":"Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines","date_created":"2021-05-26T10:48:33Z","author":[{"last_name":"Tussing","full_name":"Tussing, Sebastian","first_name":"Sebastian"},{"first_name":"Karl","full_name":"Kaupmees, Karl","last_name":"Kaupmees"},{"last_name":"Paradies","orcid":"0000-0002-3698-668X","full_name":"Paradies, Jan","id":"53339","first_name":"Jan"}],"date_updated":"2023-01-23T12:49:03Z","page":"7422-7426","citation":{"mla":"Tussing, Sebastian, et al. “Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines.” <i>Chemistry - A European Journal</i>, 2016, pp. 7422–26, doi:<a href=\"https://doi.org/10.1002/chem.201600716\">10.1002/chem.201600716</a>.","bibtex":"@article{Tussing_Kaupmees_Paradies_2016, title={Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines}, DOI={<a href=\"https://doi.org/10.1002/chem.201600716\">10.1002/chem.201600716</a>}, journal={Chemistry - A European Journal}, author={Tussing, Sebastian and Kaupmees, Karl and Paradies, Jan}, year={2016}, pages={7422–7426} }","short":"S. Tussing, K. Kaupmees, J. Paradies, Chemistry - A European Journal (2016) 7422–7426.","apa":"Tussing, S., Kaupmees, K., &#38; Paradies, J. (2016). Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines. <i>Chemistry - A European Journal</i>, 7422–7426. <a href=\"https://doi.org/10.1002/chem.201600716\">https://doi.org/10.1002/chem.201600716</a>","ieee":"S. Tussing, K. Kaupmees, and J. Paradies, “Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines,” <i>Chemistry - A European Journal</i>, pp. 7422–7426, 2016, doi: <a href=\"https://doi.org/10.1002/chem.201600716\">10.1002/chem.201600716</a>.","chicago":"Tussing, Sebastian, Karl Kaupmees, and Jan Paradies. “Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines.” <i>Chemistry - A European Journal</i>, 2016, 7422–26. <a href=\"https://doi.org/10.1002/chem.201600716\">https://doi.org/10.1002/chem.201600716</a>.","ama":"Tussing S, Kaupmees K, Paradies J. Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines. <i>Chemistry - A European Journal</i>. Published online 2016:7422-7426. doi:<a href=\"https://doi.org/10.1002/chem.201600716\">10.1002/chem.201600716</a>"},"year":"2016","publication_identifier":{"issn":["0947-6539"]},"publication_status":"published"},{"publication_status":"published","publication_identifier":{"issn":["0947-6539"]},"citation":{"mla":"Oechsle, Peter, et al. “Heteroacene Synthesis through C−S Cross-Coupling/5-Endo-DigCyclization.” <i>Chemistry - A European Journal</i>, 2016, pp. 18559–63, doi:<a href=\"https://doi.org/10.1002/chem.201603737\">10.1002/chem.201603737</a>.","short":"P. Oechsle, U. Flörke, H. Egold, J. Paradies, Chemistry - A European Journal (2016) 18559–18563.","bibtex":"@article{Oechsle_Flörke_Egold_Paradies_2016, title={Heteroacene Synthesis through C−S Cross-Coupling/5-endo-digCyclization}, DOI={<a href=\"https://doi.org/10.1002/chem.201603737\">10.1002/chem.201603737</a>}, journal={Chemistry - A European Journal}, author={Oechsle, Peter and Flörke, Ulrich and Egold, Hans and Paradies, Jan}, year={2016}, pages={18559–18563} }","apa":"Oechsle, P., Flörke, U., Egold, H., &#38; Paradies, J. (2016). Heteroacene Synthesis through C−S Cross-Coupling/5-endo-digCyclization. <i>Chemistry - A European Journal</i>, 18559–18563. <a href=\"https://doi.org/10.1002/chem.201603737\">https://doi.org/10.1002/chem.201603737</a>","ama":"Oechsle P, Flörke U, Egold H, Paradies J. Heteroacene Synthesis through C−S Cross-Coupling/5-endo-digCyclization. <i>Chemistry - A European Journal</i>. Published online 2016:18559-18563. doi:<a href=\"https://doi.org/10.1002/chem.201603737\">10.1002/chem.201603737</a>","ieee":"P. Oechsle, U. Flörke, H. Egold, and J. Paradies, “Heteroacene Synthesis through C−S Cross-Coupling/5-endo-digCyclization,” <i>Chemistry - A European Journal</i>, pp. 18559–18563, 2016, doi: <a href=\"https://doi.org/10.1002/chem.201603737\">10.1002/chem.201603737</a>.","chicago":"Oechsle, Peter, Ulrich Flörke, Hans Egold, and Jan Paradies. “Heteroacene Synthesis through C−S Cross-Coupling/5-Endo-DigCyclization.” <i>Chemistry - A European Journal</i>, 2016, 18559–63. <a href=\"https://doi.org/10.1002/chem.201603737\">https://doi.org/10.1002/chem.201603737</a>."},"page":"18559-18563","year":"2016","date_created":"2021-05-26T10:44:00Z","author":[{"first_name":"Peter","last_name":"Oechsle","full_name":"Oechsle, Peter"},{"first_name":"Ulrich","last_name":"Flörke","full_name":"Flörke, Ulrich"},{"full_name":"Egold, Hans","last_name":"Egold","first_name":"Hans"},{"first_name":"Jan","id":"53339","full_name":"Paradies, Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X"}],"date_updated":"2023-01-23T12:49:39Z","doi":"10.1002/chem.201603737","title":"Heteroacene Synthesis through C−S Cross-Coupling/5-endo-digCyclization","type":"journal_article","publication":"Chemistry - A European Journal","status":"public","user_id":"53339","_id":"22248","language":[{"iso":"eng"}]},{"language":[{"iso":"eng"}],"keyword":["General Chemistry","Catalysis","Organic Chemistry"],"user_id":"53339","department":[{"_id":"2"},{"_id":"389"}],"_id":"35710","status":"public","type":"journal_article","publication":"Chemistry – A European Journal","doi":"10.1002/chem.201601558","title":"Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016)","author":[{"first_name":"Sebastian","full_name":"Tussing, Sebastian","last_name":"Tussing"},{"first_name":"Karl","full_name":"Kaupmees, Karl","last_name":"Kaupmees"},{"id":"53339","full_name":"Paradies, Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan"}],"date_created":"2023-01-10T09:13:44Z","volume":22,"date_updated":"2023-01-23T12:54:23Z","publisher":"Wiley","citation":{"short":"S. Tussing, K. Kaupmees, J. Paradies, Chemistry – A European Journal 22 (2016) 7302–7302.","mla":"Tussing, Sebastian, et al. “Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016).” <i>Chemistry – A European Journal</i>, vol. 22, no. 22, Wiley, 2016, pp. 7302–7302, doi:<a href=\"https://doi.org/10.1002/chem.201601558\">10.1002/chem.201601558</a>.","bibtex":"@article{Tussing_Kaupmees_Paradies_2016, title={Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016)}, volume={22}, DOI={<a href=\"https://doi.org/10.1002/chem.201601558\">10.1002/chem.201601558</a>}, number={22}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Tussing, Sebastian and Kaupmees, Karl and Paradies, Jan}, year={2016}, pages={7302–7302} }","apa":"Tussing, S., Kaupmees, K., &#38; Paradies, J. (2016). Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016). <i>Chemistry – A European Journal</i>, <i>22</i>(22), 7302–7302. <a href=\"https://doi.org/10.1002/chem.201601558\">https://doi.org/10.1002/chem.201601558</a>","ama":"Tussing S, Kaupmees K, Paradies J. Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016). <i>Chemistry – A European Journal</i>. 2016;22(22):7302-7302. doi:<a href=\"https://doi.org/10.1002/chem.201601558\">10.1002/chem.201601558</a>","ieee":"S. Tussing, K. Kaupmees, and J. Paradies, “Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016),” <i>Chemistry – A European Journal</i>, vol. 22, no. 22, pp. 7302–7302, 2016, doi: <a href=\"https://doi.org/10.1002/chem.201601558\">10.1002/chem.201601558</a>.","chicago":"Tussing, Sebastian, Karl Kaupmees, and Jan Paradies. “Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016).” <i>Chemistry – A European Journal</i> 22, no. 22 (2016): 7302–7302. <a href=\"https://doi.org/10.1002/chem.201601558\">https://doi.org/10.1002/chem.201601558</a>."},"intvolume":"        22","page":"7302-7302","year":"2016","issue":"22","publication_status":"published","publication_identifier":{"issn":["0947-6539","1521-3765"]}},{"date_created":"2021-05-26T10:53:04Z","author":[{"last_name":"Tussing","full_name":"Tussing, Sebastian","first_name":"Sebastian"},{"first_name":"Karl","full_name":"Kaupmees, Karl","last_name":"Kaupmees"},{"full_name":"Paradies, Jan","id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan"}],"date_updated":"2023-01-23T12:54:18Z","doi":"10.1002/chem.201601558","title":"Inside Cover: Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016)","publication_identifier":{"issn":["0947-6539"]},"publication_status":"published","page":"7302-7302","citation":{"ama":"Tussing S, Kaupmees K, Paradies J. Inside Cover: Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016). <i>Chemistry - A European Journal</i>. Published online 2016:7302-7302. doi:<a href=\"https://doi.org/10.1002/chem.201601558\">10.1002/chem.201601558</a>","chicago":"Tussing, Sebastian, Karl Kaupmees, and Jan Paradies. “Inside Cover: Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016).” <i>Chemistry - A European Journal</i>, 2016, 7302–7302. <a href=\"https://doi.org/10.1002/chem.201601558\">https://doi.org/10.1002/chem.201601558</a>.","ieee":"S. Tussing, K. Kaupmees, and J. Paradies, “Inside Cover: Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016),” <i>Chemistry - A European Journal</i>, pp. 7302–7302, 2016, doi: <a href=\"https://doi.org/10.1002/chem.201601558\">10.1002/chem.201601558</a>.","apa":"Tussing, S., Kaupmees, K., &#38; Paradies, J. (2016). Inside Cover: Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016). <i>Chemistry - A European Journal</i>, 7302–7302. <a href=\"https://doi.org/10.1002/chem.201601558\">https://doi.org/10.1002/chem.201601558</a>","short":"S. Tussing, K. Kaupmees, J. Paradies, Chemistry - A European Journal (2016) 7302–7302.","mla":"Tussing, Sebastian, et al. “Inside Cover: Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016).” <i>Chemistry - A European Journal</i>, 2016, pp. 7302–7302, doi:<a href=\"https://doi.org/10.1002/chem.201601558\">10.1002/chem.201601558</a>.","bibtex":"@article{Tussing_Kaupmees_Paradies_2016, title={Inside Cover: Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016)}, DOI={<a href=\"https://doi.org/10.1002/chem.201601558\">10.1002/chem.201601558</a>}, journal={Chemistry - A European Journal}, author={Tussing, Sebastian and Kaupmees, Karl and Paradies, Jan}, year={2016}, pages={7302–7302} }"},"year":"2016","user_id":"53339","_id":"22257","language":[{"iso":"eng"}],"publication":"Chemistry - A European Journal","type":"journal_article","status":"public"},{"doi":"10.1002/nadc.20164047492","title":"Organische Chemie","author":[{"first_name":"Aymelt","last_name":"Itzen","full_name":"Itzen, Aymelt"},{"last_name":"Schaschke","full_name":"Schaschke, Norbert","first_name":"Norbert"},{"first_name":"Uwe","last_name":"Beifuss","full_name":"Beifuss, Uwe"},{"first_name":"Matthias","last_name":"Lehmann","full_name":"Lehmann, Matthias"},{"full_name":"Krueger, Anke","last_name":"Krueger","first_name":"Anke"},{"first_name":"Florian","last_name":"Beuerle","full_name":"Beuerle, Florian"},{"last_name":"Senge","full_name":"Senge, Mathias O.","first_name":"Mathias O."},{"last_name":"Breinbauer","full_name":"Breinbauer, Rolf","first_name":"Rolf"},{"first_name":"Christian","last_name":"Mück‐Lichtenfeld","full_name":"Mück‐Lichtenfeld, Christian"},{"first_name":"Thomas J. J.","last_name":"Müller","full_name":"Müller, Thomas J. J."},{"first_name":"Melanie","full_name":"Denißen, Melanie","last_name":"Denißen"},{"first_name":"Thomas","last_name":"Lindel","full_name":"Lindel, Thomas"},{"first_name":"Jörg","last_name":"Pietruszka","full_name":"Pietruszka, Jörg"},{"full_name":"Worgull, Dennis","last_name":"Worgull","first_name":"Dennis"},{"first_name":"Tobias","full_name":"Gulder, Tobias","last_name":"Gulder"},{"orcid":"0000-0002-3698-668X","last_name":"Paradies","id":"53339","full_name":"Paradies, Jan","first_name":"Jan"},{"first_name":"Kilian","last_name":"Muñiz","full_name":"Muñiz, Kilian"},{"first_name":"Thorsten","last_name":"Bach","full_name":"Bach, Thorsten"},{"first_name":"Klaus","full_name":"Ditrich, Klaus","last_name":"Ditrich"},{"first_name":"Christian","full_name":"Winter, Christian","last_name":"Winter"},{"first_name":"Markus","last_name":"Kordes","full_name":"Kordes, Markus"},{"last_name":"von Deyn","full_name":"von Deyn, Wolfgang","first_name":"Wolfgang"},{"last_name":"Pfau","full_name":"Pfau, Roland","first_name":"Roland"},{"first_name":"Claudia","last_name":"Muhle‐Goll","full_name":"Muhle‐Goll, Claudia"},{"first_name":"Burkhard","last_name":"Luy","full_name":"Luy, Burkhard"},{"first_name":"Daniel B.","last_name":"Werz","full_name":"Werz, Daniel B."},{"full_name":"Arenz, Christoph","last_name":"Arenz","first_name":"Christoph"},{"first_name":"Wolfgang","last_name":"Hüttel","full_name":"Hüttel, Wolfgang"},{"first_name":"Jennifer N.","full_name":"Andexer, Jennifer N.","last_name":"Andexer"},{"full_name":"Straub, Bernd F.","last_name":"Straub","first_name":"Bernd F."}],"date_created":"2026-03-11T10:25:12Z","volume":64,"date_updated":"2026-03-11T10:25:23Z","publisher":"Wiley","citation":{"apa":"Itzen, A., Schaschke, N., Beifuss, U., Lehmann, M., Krueger, A., Beuerle, F., Senge, M. O., Breinbauer, R., Mück‐Lichtenfeld, C., Müller, T. J. J., Denißen, M., Lindel, T., Pietruszka, J., Worgull, D., Gulder, T., Paradies, J., Muñiz, K., Bach, T., Ditrich, K., … Straub, B. F. (2016). Organische Chemie. <i>Nachrichten Aus Der Chemie</i>, <i>64</i>(3), 255–294. <a href=\"https://doi.org/10.1002/nadc.20164047492\">https://doi.org/10.1002/nadc.20164047492</a>","short":"A. Itzen, N. Schaschke, U. Beifuss, M. Lehmann, A. Krueger, F. Beuerle, M.O. Senge, R. Breinbauer, C. Mück‐Lichtenfeld, T.J.J. Müller, M. Denißen, T. Lindel, J. Pietruszka, D. Worgull, T. Gulder, J. Paradies, K. Muñiz, T. Bach, K. Ditrich, C. Winter, M. Kordes, W. von Deyn, R. Pfau, C. Muhle‐Goll, B. Luy, D.B. Werz, C. Arenz, W. Hüttel, J.N. Andexer, B.F. Straub, Nachrichten Aus Der Chemie 64 (2016) 255–294.","bibtex":"@article{Itzen_Schaschke_Beifuss_Lehmann_Krueger_Beuerle_Senge_Breinbauer_Mück‐Lichtenfeld_Müller_et al._2016, title={Organische Chemie}, volume={64}, DOI={<a href=\"https://doi.org/10.1002/nadc.20164047492\">10.1002/nadc.20164047492</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Itzen, Aymelt and Schaschke, Norbert and Beifuss, Uwe and Lehmann, Matthias and Krueger, Anke and Beuerle, Florian and Senge, Mathias O. and Breinbauer, Rolf and Mück‐Lichtenfeld, Christian and Müller, Thomas J. J. and et al.}, year={2016}, pages={255–294} }","mla":"Itzen, Aymelt, et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i>, vol. 64, no. 3, Wiley, 2016, pp. 255–94, doi:<a href=\"https://doi.org/10.1002/nadc.20164047492\">10.1002/nadc.20164047492</a>.","ieee":"A. Itzen <i>et al.</i>, “Organische Chemie,” <i>Nachrichten aus der Chemie</i>, vol. 64, no. 3, pp. 255–294, 2016, doi: <a href=\"https://doi.org/10.1002/nadc.20164047492\">10.1002/nadc.20164047492</a>.","chicago":"Itzen, Aymelt, Norbert Schaschke, Uwe Beifuss, Matthias Lehmann, Anke Krueger, Florian Beuerle, Mathias O. Senge, et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i> 64, no. 3 (2016): 255–94. <a href=\"https://doi.org/10.1002/nadc.20164047492\">https://doi.org/10.1002/nadc.20164047492</a>.","ama":"Itzen A, Schaschke N, Beifuss U, et al. Organische Chemie. <i>Nachrichten aus der Chemie</i>. 2016;64(3):255-294. doi:<a href=\"https://doi.org/10.1002/nadc.20164047492\">10.1002/nadc.20164047492</a>"},"page":"255-294","intvolume":"        64","year":"2016","issue":"3","publication_status":"published","publication_identifier":{"issn":["1439-9598","1868-0054"]},"language":[{"iso":"eng"}],"user_id":"53339","department":[{"_id":"2"},{"_id":"389"}],"_id":"64898","status":"public","abstract":[{"lang":"eng","text":"<jats:title>Abstract</jats:title><jats:p>Siliciumrhodaminderivate weisen Formaldehyd nach – neues Nanomaterial: Graphitphasen polymeren Kohlenstoffnitrids – molekulare Drähte – homogene Cof‐Dünnschichten bei Raumtemperatur – Biosyntheserekord: 1,8 MDa großes kolGen – [3,3]‐sigmatrope Umlagerung führt zu quartären Stereozentren.</jats:p>"}],"type":"journal_article","publication":"Nachrichten aus der Chemie"},{"publication_identifier":{"isbn":["9783527336890","9783527681020"]},"publication_status":"published","citation":{"apa":"Paradies, J. (2015). Cooperative H            <sub>2</sub>            Activation by Borane‐Derived Frustrated Lewis Pairs. In <i>Cooperative Catalysis</i>. Wiley. <a href=\"https://doi.org/10.1002/9783527681020.ch9\">https://doi.org/10.1002/9783527681020.ch9</a>","mla":"Paradies, Jan. “Cooperative H            <sub>2</sub>            Activation by Borane‐Derived Frustrated Lewis Pairs.” <i>Cooperative Catalysis</i>, Wiley, 2015, doi:<a href=\"https://doi.org/10.1002/9783527681020.ch9\">10.1002/9783527681020.ch9</a>.","bibtex":"@inbook{Paradies_2015, title={Cooperative H            <sub>2</sub>            Activation by Borane‐Derived Frustrated Lewis Pairs}, DOI={<a href=\"https://doi.org/10.1002/9783527681020.ch9\">10.1002/9783527681020.ch9</a>}, booktitle={Cooperative Catalysis}, publisher={Wiley}, author={Paradies, Jan}, year={2015} }","short":"J. Paradies, in: Cooperative Catalysis, Wiley, 2015.","ieee":"J. Paradies, “Cooperative H            <sub>2</sub>            Activation by Borane‐Derived Frustrated Lewis Pairs,” in <i>Cooperative Catalysis</i>, Wiley, 2015.","chicago":"Paradies, Jan. “Cooperative H            <sub>2</sub>            Activation by Borane‐Derived Frustrated Lewis Pairs.” In <i>Cooperative Catalysis</i>. Wiley, 2015. <a href=\"https://doi.org/10.1002/9783527681020.ch9\">https://doi.org/10.1002/9783527681020.ch9</a>.","ama":"Paradies J. Cooperative H            <sub>2</sub>            Activation by Borane‐Derived Frustrated Lewis Pairs. In: <i>Cooperative Catalysis</i>. Wiley; 2015. doi:<a href=\"https://doi.org/10.1002/9783527681020.ch9\">10.1002/9783527681020.ch9</a>"},"year":"2015","date_created":"2026-03-11T10:16:38Z","author":[{"first_name":"Jan","full_name":"Paradies, Jan","id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X"}],"publisher":"Wiley","date_updated":"2026-03-11T10:16:44Z","doi":"10.1002/9783527681020.ch9","title":"Cooperative H            <sub>2</sub>            Activation by Borane‐Derived Frustrated Lewis Pairs","publication":"Cooperative Catalysis","type":"book_chapter","status":"public","department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339","_id":"64889","language":[{"iso":"eng"}]},{"department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339","_id":"64891","language":[{"iso":"eng"}],"article_number":"chin.201425048","publication":"ChemInform","type":"journal_article","status":"public","abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>The dehydrocoupling of hydrosilanes with anilines, carbazoles and indoles is reported.</jats:p>","lang":"eng"}],"volume":45,"author":[{"full_name":"Greb, Lutz","last_name":"Greb","first_name":"Lutz"},{"last_name":"Tamke","full_name":"Tamke, Sergej","first_name":"Sergej"},{"id":"53339","full_name":"Paradies, Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan"}],"date_created":"2026-03-11T10:18:20Z","date_updated":"2026-03-11T10:18:29Z","publisher":"Wiley","doi":"10.1002/chin.201425048","title":"ChemInform Abstract: Catalytic Metal‐Free Si—N Cross‐Dehydrocoupling.","issue":"25","publication_identifier":{"issn":["0931-7597","1522-2667"]},"publication_status":"published","intvolume":"        45","citation":{"apa":"Greb, L., Tamke, S., &#38; Paradies, J. (2014). ChemInform Abstract: Catalytic Metal‐Free Si—N Cross‐Dehydrocoupling. <i>ChemInform</i>, <i>45</i>(25), Article chin. 201425048. <a href=\"https://doi.org/10.1002/chin.201425048\">https://doi.org/10.1002/chin.201425048</a>","short":"L. Greb, S. Tamke, J. Paradies, ChemInform 45 (2014).","bibtex":"@article{Greb_Tamke_Paradies_2014, title={ChemInform Abstract: Catalytic Metal‐Free Si—N Cross‐Dehydrocoupling.}, volume={45}, DOI={<a href=\"https://doi.org/10.1002/chin.201425048\">10.1002/chin.201425048</a>}, number={25chin. 201425048}, journal={ChemInform}, publisher={Wiley}, author={Greb, Lutz and Tamke, Sergej and Paradies, Jan}, year={2014} }","mla":"Greb, Lutz, et al. “ChemInform Abstract: Catalytic Metal‐Free Si—N Cross‐Dehydrocoupling.” <i>ChemInform</i>, vol. 45, no. 25, chin. 201425048, Wiley, 2014, doi:<a href=\"https://doi.org/10.1002/chin.201425048\">10.1002/chin.201425048</a>.","ama":"Greb L, Tamke S, Paradies J. ChemInform Abstract: Catalytic Metal‐Free Si—N Cross‐Dehydrocoupling. <i>ChemInform</i>. 2014;45(25). doi:<a href=\"https://doi.org/10.1002/chin.201425048\">10.1002/chin.201425048</a>","chicago":"Greb, Lutz, Sergej Tamke, and Jan Paradies. “ChemInform Abstract: Catalytic Metal‐Free Si—N Cross‐Dehydrocoupling.” <i>ChemInform</i> 45, no. 25 (2014). <a href=\"https://doi.org/10.1002/chin.201425048\">https://doi.org/10.1002/chin.201425048</a>.","ieee":"L. Greb, S. Tamke, and J. Paradies, “ChemInform Abstract: Catalytic Metal‐Free Si—N Cross‐Dehydrocoupling.,” <i>ChemInform</i>, vol. 45, no. 25, Art. no. chin. 201425048, 2014, doi: <a href=\"https://doi.org/10.1002/chin.201425048\">10.1002/chin.201425048</a>."},"year":"2014"},{"doi":"10.1002/chin.201423263","title":"ChemInform Abstract: Metal‐Free Hydrogenation of Unsaturated Hydrocarbons Employing Molecular Hydrogen","volume":45,"date_created":"2026-03-11T10:18:53Z","author":[{"first_name":"Jan","id":"53339","full_name":"Paradies, Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies"}],"publisher":"Wiley","date_updated":"2026-03-11T10:18:59Z","intvolume":"        45","citation":{"short":"J. Paradies, ChemInform 45 (2014).","bibtex":"@article{Paradies_2014, title={ChemInform Abstract: Metal‐Free Hydrogenation of Unsaturated Hydrocarbons Employing Molecular Hydrogen}, volume={45}, DOI={<a href=\"https://doi.org/10.1002/chin.201423263\">10.1002/chin.201423263</a>}, number={23chin. 201423263}, journal={ChemInform}, publisher={Wiley}, author={Paradies, Jan}, year={2014} }","mla":"Paradies, Jan. “ChemInform Abstract: Metal‐Free Hydrogenation of Unsaturated Hydrocarbons Employing Molecular Hydrogen.” <i>ChemInform</i>, vol. 45, no. 23, chin. 201423263, Wiley, 2014, doi:<a href=\"https://doi.org/10.1002/chin.201423263\">10.1002/chin.201423263</a>.","apa":"Paradies, J. (2014). ChemInform Abstract: Metal‐Free Hydrogenation of Unsaturated Hydrocarbons Employing Molecular Hydrogen. <i>ChemInform</i>, <i>45</i>(23), Article chin. 201423263. <a href=\"https://doi.org/10.1002/chin.201423263\">https://doi.org/10.1002/chin.201423263</a>","chicago":"Paradies, Jan. “ChemInform Abstract: Metal‐Free Hydrogenation of Unsaturated Hydrocarbons Employing Molecular Hydrogen.” <i>ChemInform</i> 45, no. 23 (2014). <a href=\"https://doi.org/10.1002/chin.201423263\">https://doi.org/10.1002/chin.201423263</a>.","ieee":"J. Paradies, “ChemInform Abstract: Metal‐Free Hydrogenation of Unsaturated Hydrocarbons Employing Molecular Hydrogen,” <i>ChemInform</i>, vol. 45, no. 23, Art. no. chin. 201423263, 2014, doi: <a href=\"https://doi.org/10.1002/chin.201423263\">10.1002/chin.201423263</a>.","ama":"Paradies J. ChemInform Abstract: Metal‐Free Hydrogenation of Unsaturated Hydrocarbons Employing Molecular Hydrogen. <i>ChemInform</i>. 2014;45(23). doi:<a href=\"https://doi.org/10.1002/chin.201423263\">10.1002/chin.201423263</a>"},"year":"2014","issue":"23","publication_identifier":{"issn":["0931-7597","1522-2667"]},"publication_status":"published","language":[{"iso":"eng"}],"article_number":"chin.201423263","department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339","_id":"64892","status":"public","abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>Review: [41 refs.</jats:p>","lang":"eng"}],"publication":"ChemInform","type":"journal_article"},{"user_id":"53339","department":[{"_id":"2"},{"_id":"389"}],"_id":"64901","language":[{"iso":"eng"}],"type":"book_chapter","publication":"Topics in Current Chemistry","status":"public","date_created":"2026-03-11T10:32:32Z","author":[{"first_name":"Lutz","last_name":"Greb","full_name":"Greb, Lutz"},{"id":"53339","full_name":"Paradies, Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies","first_name":"Jan"}],"date_updated":"2026-03-11T10:32:41Z","publisher":"Springer Berlin Heidelberg","doi":"10.1007/128_2012_375","title":"Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry","publication_status":"published","publication_identifier":{"issn":["0340-1022","1436-5049"],"isbn":["9783642377587","9783642377594"]},"citation":{"ama":"Greb L, Paradies J. Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry. In: <i>Topics in Current Chemistry</i>. Springer Berlin Heidelberg; 2012. doi:<a href=\"https://doi.org/10.1007/128_2012_375\">10.1007/128_2012_375</a>","ieee":"L. Greb and J. Paradies, “Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry,” in <i>Topics in Current Chemistry</i>, Berlin, Heidelberg: Springer Berlin Heidelberg, 2012.","chicago":"Greb, Lutz, and Jan Paradies. “Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry.” In <i>Topics in Current Chemistry</i>. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. <a href=\"https://doi.org/10.1007/128_2012_375\">https://doi.org/10.1007/128_2012_375</a>.","short":"L. Greb, J. Paradies, in: Topics in Current Chemistry, Springer Berlin Heidelberg, Berlin, Heidelberg, 2012.","bibtex":"@inbook{Greb_Paradies_2012, place={Berlin, Heidelberg}, title={Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry}, DOI={<a href=\"https://doi.org/10.1007/128_2012_375\">10.1007/128_2012_375</a>}, booktitle={Topics in Current Chemistry}, publisher={Springer Berlin Heidelberg}, author={Greb, Lutz and Paradies, Jan}, year={2012} }","mla":"Greb, Lutz, and Jan Paradies. “Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry.” <i>Topics in Current Chemistry</i>, Springer Berlin Heidelberg, 2012, doi:<a href=\"https://doi.org/10.1007/128_2012_375\">10.1007/128_2012_375</a>.","apa":"Greb, L., &#38; Paradies, J. (2012). Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry. In <i>Topics in Current Chemistry</i>. Springer Berlin Heidelberg. <a href=\"https://doi.org/10.1007/128_2012_375\">https://doi.org/10.1007/128_2012_375</a>"},"year":"2012","place":"Berlin, Heidelberg"}]