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Published online 2017:1539-1545. doi:<a href=\"https://doi.org/10.1039/c6dt04725d\">10.1039/c6dt04725d</a>"},"date_updated":"2023-01-23T12:49:49Z","date_created":"2021-05-26T10:43:41Z","author":[{"last_name":"Tussing","full_name":"Tussing, Sebastian","first_name":"Sebastian"},{"first_name":"Miriam","full_name":"Ohland, Miriam","last_name":"Ohland"},{"first_name":"Garrit","full_name":"Wicker, Garrit","last_name":"Wicker"},{"first_name":"Ulrich","last_name":"Flörke","full_name":"Flörke, Ulrich"},{"first_name":"Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies","full_name":"Paradies, Jan","id":"53339"}],"title":"Borane-catalyzed indole synthesis through intramolecular hydroamination","doi":"10.1039/c6dt04725d","publication":"Dalton Transactions","type":"journal_article","abstract":[{"text":"<p>Catalytic metal-free intramolecular hydroamination for the synthesis of indoles and tetrahydroisoquinolines was achieved.</p>","lang":"eng"}],"status":"public","_id":"22247","user_id":"53339","language":[{"iso":"eng"}]},{"publication_identifier":{"issn":["1434-1948"]},"publication_status":"published","page":"3053-3056","citation":{"apa":"Bader, J., Maier, A. 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Paradies, Nachrichten Aus Der Chemie 65 (2017) 118–122.","bibtex":"@article{Paradies_2017, title={Reaktivität verstehen, ohne die Katalysatorstruktur zu kennen}, volume={65}, DOI={<a href=\"https://doi.org/10.1002/nadc.20174055283\">10.1002/nadc.20174055283</a>}, number={2}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Paradies, Jan}, year={2017}, pages={118–122} }","mla":"Paradies, Jan. “Reaktivität Verstehen, Ohne Die Katalysatorstruktur Zu Kennen.” <i>Nachrichten Aus Der Chemie</i>, vol. 65, no. 2, Wiley, 2017, pp. 118–22, doi:<a href=\"https://doi.org/10.1002/nadc.20174055283\">10.1002/nadc.20174055283</a>.","apa":"Paradies, J. (2017). Reaktivität verstehen, ohne die Katalysatorstruktur zu kennen. <i>Nachrichten Aus Der Chemie</i>, <i>65</i>(2), 118–122. <a href=\"https://doi.org/10.1002/nadc.20174055283\">https://doi.org/10.1002/nadc.20174055283</a>","chicago":"Paradies, Jan. “Reaktivität Verstehen, Ohne Die Katalysatorstruktur Zu Kennen.” <i>Nachrichten Aus Der Chemie</i> 65, no. 2 (2017): 118–22. <a href=\"https://doi.org/10.1002/nadc.20174055283\">https://doi.org/10.1002/nadc.20174055283</a>.","ieee":"J. Paradies, “Reaktivität verstehen, ohne die Katalysatorstruktur zu kennen,” <i>Nachrichten aus der Chemie</i>, vol. 65, no. 2, pp. 118–122, 2017, doi: <a href=\"https://doi.org/10.1002/nadc.20174055283\">10.1002/nadc.20174055283</a>.","ama":"Paradies J. Reaktivität verstehen, ohne die Katalysatorstruktur zu kennen. <i>Nachrichten aus der Chemie</i>. 2017;65(2):118-122. doi:<a href=\"https://doi.org/10.1002/nadc.20174055283\">10.1002/nadc.20174055283</a>"},"page":"118-122","intvolume":"        65","year":"2017","user_id":"53339","department":[{"_id":"2"},{"_id":"389"}],"_id":"64888","language":[{"iso":"eng"}],"type":"journal_article","publication":"Nachrichten aus der Chemie","status":"public","abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>Manche boranbasierten frustrierten Lewis‐Paare spalten Wasserstoff – wie, war bislang unklar. Um Struktur und Reaktivität in Beziehung zu setzen, werden quantenchemische Untersuchungen und NMR‐Experimente kombiniert. Sind pK<jats:sub>a</jats:sub>‐Werte der Lewis‐Base bekannt, lässt sich damit Reaktivität vorhersagen.</jats:p>","lang":"eng"}]},{"title":"Organische Chemie 2016","doi":"10.1002/nadc.20174059831","date_updated":"2026-03-11T10:26:39Z","publisher":"Wiley","volume":65,"author":[{"full_name":"Straub, Bernd F.","last_name":"Straub","first_name":"Bernd F."},{"last_name":"Andexer","full_name":"Andexer, Jennifer","first_name":"Jennifer"},{"full_name":"Arenz, Christoph","last_name":"Arenz","first_name":"Christoph"},{"first_name":"Uwe","full_name":"Beifuss, Uwe","last_name":"Beifuss"},{"full_name":"Beuerle, Florian","last_name":"Beuerle","first_name":"Florian"},{"full_name":"Brasholz, Malte","last_name":"Brasholz","first_name":"Malte"},{"last_name":"Breinbauer","full_name":"Breinbauer, Rolf","first_name":"Rolf"},{"first_name":"Klaus","full_name":"Ditrich, Klaus","last_name":"Ditrich"},{"full_name":"Gulder, Tobias A. M.","last_name":"Gulder","first_name":"Tobias A. 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Straub <i>et al.</i>, “Organische Chemie 2016,” <i>Nachrichten aus der Chemie</i>, vol. 65, no. 3, pp. 266–304, 2017, doi: <a href=\"https://doi.org/10.1002/nadc.20174059831\">10.1002/nadc.20174059831</a>.","chicago":"Straub, Bernd F., Jennifer Andexer, Christoph Arenz, Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, et al. “Organische Chemie 2016.” <i>Nachrichten Aus Der Chemie</i> 65, no. 3 (2017): 266–304. <a href=\"https://doi.org/10.1002/nadc.20174059831\">https://doi.org/10.1002/nadc.20174059831</a>.","short":"B.F. Straub, J. Andexer, C. Arenz, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, K. Ditrich, T.A.M. Gulder, W. Hüttel, M. Kordes, A. Krueger, M. Lehmann, T. Lindel, B. Luy, M.A.R. Meier, C. Mück-Lichtenfeld, C. Muhle-Goll, T.J.J. Müller, A. Narine, J. Paradies, R. Pfau, J. Pietruszka, N. Schaschke, M.O. Senge, T. Werner, D.B. Werz, C.A. Winter, D. 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Springer International Publishing; 2017. doi:<a href=\"https://doi.org/10.1007/3418_2016_173\">10.1007/3418_2016_173</a>","chicago":"Paradies, Jan. “Chiral Borane-Based Lewis Acids for Metal Free Hydrogenations.” In <i>Topics in Organometallic Chemistry</i>. Cham: Springer International Publishing, 2017. <a href=\"https://doi.org/10.1007/3418_2016_173\">https://doi.org/10.1007/3418_2016_173</a>.","ieee":"J. Paradies, “Chiral Borane-Based Lewis Acids for Metal Free Hydrogenations,” in <i>Topics in Organometallic Chemistry</i>, Cham: Springer International Publishing, 2017.","apa":"Paradies, J. (2017). Chiral Borane-Based Lewis Acids for Metal Free Hydrogenations. In <i>Topics in Organometallic Chemistry</i>. 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