{"user_id":"53339","language":[{"iso":"eng"}],"title":"Diastereoselective Synthesis of Dihydro-quinolin-4-ones by a Borane-Catalyzed Redox-Neutral endo-1,7-Hydride Shift","_id":"22232","type":"journal_article","publication_identifier":{"issn":["1523-7060","1523-7052"]},"status":"public","publication":"Organic Letters","publication_status":"published","page":"3626-3630","author":[{"last_name":"Wicker","first_name":"Garrit","full_name":"Wicker, Garrit"},{"first_name":"Roland","full_name":"Schoch, Roland","last_name":"Schoch"},{"last_name":"Paradies","first_name":"Jan","full_name":"Paradies, Jan"}],"citation":{"short":"G. Wicker, R. Schoch, J. Paradies, Organic Letters (2021) 3626–3630.","mla":"Wicker, Garrit, et al. “Diastereoselective Synthesis of Dihydro-Quinolin-4-Ones by a Borane-Catalyzed Redox-Neutral Endo-1,7-Hydride Shift.” <i>Organic Letters</i>, 2021, pp. 3626–30, doi:<a href=\"https://doi.org/10.1021/acs.orglett.1c01018\">10.1021/acs.orglett.1c01018</a>.","apa":"Wicker, G., Schoch, R., &#38; Paradies, J. (2021). Diastereoselective Synthesis of Dihydro-quinolin-4-ones by a Borane-Catalyzed Redox-Neutral endo-1,7-Hydride Shift. <i>Organic Letters</i>, 3626–3630. <a href=\"https://doi.org/10.1021/acs.orglett.1c01018\">https://doi.org/10.1021/acs.orglett.1c01018</a>","bibtex":"@article{Wicker_Schoch_Paradies_2021, title={Diastereoselective Synthesis of Dihydro-quinolin-4-ones by a Borane-Catalyzed Redox-Neutral endo-1,7-Hydride Shift}, DOI={<a href=\"https://doi.org/10.1021/acs.orglett.1c01018\">10.1021/acs.orglett.1c01018</a>}, journal={Organic Letters}, author={Wicker, Garrit and Schoch, Roland and Paradies, Jan}, year={2021}, pages={3626–3630} }","ama":"Wicker G, Schoch R, Paradies J. Diastereoselective Synthesis of Dihydro-quinolin-4-ones by a Borane-Catalyzed Redox-Neutral endo-1,7-Hydride Shift. <i>Organic Letters</i>. 2021:3626-3630. doi:<a href=\"https://doi.org/10.1021/acs.orglett.1c01018\">10.1021/acs.orglett.1c01018</a>","ieee":"G. Wicker, R. Schoch, and J. Paradies, “Diastereoselective Synthesis of Dihydro-quinolin-4-ones by a Borane-Catalyzed Redox-Neutral endo-1,7-Hydride Shift,” <i>Organic Letters</i>, pp. 3626–3630, 2021.","chicago":"Wicker, Garrit, Roland Schoch, and Jan Paradies. “Diastereoselective Synthesis of Dihydro-Quinolin-4-Ones by a Borane-Catalyzed Redox-Neutral Endo-1,7-Hydride Shift.” <i>Organic Letters</i>, 2021, 3626–30. <a href=\"https://doi.org/10.1021/acs.orglett.1c01018\">https://doi.org/10.1021/acs.orglett.1c01018</a>."},"date_created":"2021-05-26T10:26:30Z","date_updated":"2022-01-06T06:55:29Z","doi":"10.1021/acs.orglett.1c01018","year":"2021"}