[{"status":"public","publisher":"American Chemical Society (ACS)","_id":"62095","page":"9114-9118","volume":25,"user_id":"89271","citation":{"chicago":"Tönjes, Jan, Lukas Kell, and Thomas Werner. “Organocatalytic Stereospecific Appel Reaction.” <i>Organic Letters</i> 25, no. 51 (2023): 9114–18. <a href=\"https://doi.org/10.1021/acs.orglett.3c03463\">https://doi.org/10.1021/acs.orglett.3c03463</a>.","short":"J. Tönjes, L. Kell, T. Werner, Organic Letters 25 (2023) 9114–9118.","ieee":"J. Tönjes, L. Kell, and T. Werner, “Organocatalytic Stereospecific Appel Reaction,” <i>Organic Letters</i>, vol. 25, no. 51, pp. 9114–9118, 2023, doi: <a href=\"https://doi.org/10.1021/acs.orglett.3c03463\">10.1021/acs.orglett.3c03463</a>.","apa":"Tönjes, J., Kell, L., &#38; Werner, T. (2023). Organocatalytic Stereospecific Appel Reaction. <i>Organic Letters</i>, <i>25</i>(51), 9114–9118. <a href=\"https://doi.org/10.1021/acs.orglett.3c03463\">https://doi.org/10.1021/acs.orglett.3c03463</a>","bibtex":"@article{Tönjes_Kell_Werner_2023, title={Organocatalytic Stereospecific Appel Reaction}, volume={25}, DOI={<a href=\"https://doi.org/10.1021/acs.orglett.3c03463\">10.1021/acs.orglett.3c03463</a>}, number={51}, journal={Organic Letters}, publisher={American Chemical Society (ACS)}, author={Tönjes, Jan and Kell, Lukas and Werner, Thomas}, year={2023}, pages={9114–9118} }","ama":"Tönjes J, Kell L, Werner T. Organocatalytic Stereospecific Appel Reaction. <i>Organic Letters</i>. 2023;25(51):9114-9118. doi:<a href=\"https://doi.org/10.1021/acs.orglett.3c03463\">10.1021/acs.orglett.3c03463</a>","mla":"Tönjes, Jan, et al. “Organocatalytic Stereospecific Appel Reaction.” <i>Organic Letters</i>, vol. 25, no. 51, American Chemical Society (ACS), 2023, pp. 9114–18, doi:<a href=\"https://doi.org/10.1021/acs.orglett.3c03463\">10.1021/acs.orglett.3c03463</a>."},"publication_identifier":{"issn":["1523-7060","1523-7052"]},"author":[{"full_name":"Tönjes, Jan","last_name":"Tönjes","first_name":"Jan"},{"full_name":"Kell, Lukas","first_name":"Lukas","last_name":"Kell"},{"full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas","id":"89271"}],"title":"Organocatalytic Stereospecific Appel Reaction","year":"2023","intvolume":"        25","date_updated":"2025-11-10T08:46:39Z","publication_status":"published","language":[{"iso":"eng"}],"doi":"10.1021/acs.orglett.3c03463","issue":"51","publication":"Organic Letters","date_created":"2025-11-05T15:22:44Z","department":[{"_id":"35"},{"_id":"2"}],"type":"journal_article","keyword":["T2","CSSD"]},{"publication_identifier":{"issn":["1523-7060","1523-7052"]},"author":[{"full_name":"Wicker, Garrit","first_name":"Garrit","last_name":"Wicker"},{"first_name":"Roland","last_name":"Schoch","full_name":"Schoch, Roland"},{"full_name":"Paradies, Jan","first_name":"Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies","id":"53339"}],"year":"2021","status":"public","title":"Diastereoselective Synthesis of Dihydro-quinolin-4-ones by a Borane-Catalyzed Redox-Neutral endo-1,7-Hydride Shift","publication_status":"published","date_updated":"2023-01-23T12:57:10Z","_id":"22232","language":[{"iso":"eng"}],"page":"3626-3630","user_id":"53339","doi":"10.1021/acs.orglett.1c01018","citation":{"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>.","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>. Published online 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, 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>","short":"G. Wicker, R. Schoch, J. Paradies, Organic Letters (2021) 3626–3630.","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>."},"publication":"Organic Letters","date_created":"2021-05-26T10:26:30Z","type":"journal_article"},{"date_created":"2023-01-22T20:59:34Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["CSSD"],"publication":"Organic Letters","issue":"10","extern":"1","language":[{"iso":"eng"}],"doi":"10.1021/acs.orglett.7b00720","author":[{"full_name":"Li, Wu","first_name":"Wu","last_name":"Li"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"publication_identifier":{"issn":["1523-7060","1523-7052"]},"year":"2017","title":"B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles","intvolume":"        19","publication_status":"published","date_updated":"2025-11-10T09:14:45Z","citation":{"bibtex":"@article{Li_Werner_2017, title={B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles}, volume={19}, DOI={<a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">10.1021/acs.orglett.7b00720</a>}, number={10}, journal={Organic Letters}, publisher={American Chemical Society (ACS)}, author={Li, Wu and Werner, Thomas}, year={2017}, pages={2568–2571} }","ama":"Li W, Werner T. B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles. <i>Organic Letters</i>. 2017;19(10):2568-2571. doi:<a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">10.1021/acs.orglett.7b00720</a>","mla":"Li, Wu, and Thomas Werner. “B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles.” <i>Organic Letters</i>, vol. 19, no. 10, American Chemical Society (ACS), 2017, pp. 2568–71, doi:<a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">10.1021/acs.orglett.7b00720</a>.","short":"W. Li, T. Werner, Organic Letters 19 (2017) 2568–2571.","chicago":"Li, Wu, and Thomas Werner. “B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles.” <i>Organic Letters</i> 19, no. 10 (2017): 2568–71. <a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">https://doi.org/10.1021/acs.orglett.7b00720</a>.","ieee":"W. Li and T. Werner, “B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles,” <i>Organic Letters</i>, vol. 19, no. 10, pp. 2568–2571, 2017, doi: <a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">10.1021/acs.orglett.7b00720</a>.","apa":"Li, W., &#38; Werner, T. (2017). B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles. <i>Organic Letters</i>, <i>19</i>(10), 2568–2571. <a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">https://doi.org/10.1021/acs.orglett.7b00720</a>"},"_id":"37976","publisher":"American Chemical Society (ACS)","page":"2568-2571","volume":19,"user_id":"89271","status":"public"},{"citation":{"mla":"Li, Wu, et al. “B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds.” <i>Organic Letters</i>, vol. 19, no. 21, American Chemical Society (ACS), 2017, pp. 5768–71, doi:<a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">10.1021/acs.orglett.7b02701</a>.","bibtex":"@article{Li_Wang_Hu_Werner_2017, title={B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds}, volume={19}, DOI={<a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">10.1021/acs.orglett.7b02701</a>}, number={21}, journal={Organic Letters}, publisher={American Chemical Society (ACS)}, author={Li, Wu and Wang, Ming-Ming and Hu, Yuya and Werner, Thomas}, year={2017}, pages={5768–5771} }","ama":"Li W, Wang M-M, Hu Y, Werner T. B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds. <i>Organic Letters</i>. 2017;19(21):5768-5771. doi:<a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">10.1021/acs.orglett.7b02701</a>","ieee":"W. Li, M.-M. Wang, Y. Hu, and T. Werner, “B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds,” <i>Organic Letters</i>, vol. 19, no. 21, pp. 5768–5771, 2017, doi: <a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">10.1021/acs.orglett.7b02701</a>.","apa":"Li, W., Wang, M.-M., Hu, Y., &#38; Werner, T. (2017). B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds. <i>Organic Letters</i>, <i>19</i>(21), 5768–5771. <a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">https://doi.org/10.1021/acs.orglett.7b02701</a>","short":"W. Li, M.-M. Wang, Y. Hu, T. Werner, Organic Letters 19 (2017) 5768–5771.","chicago":"Li, Wu, Ming-Ming Wang, Yuya Hu, and Thomas Werner. “B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds.” <i>Organic Letters</i> 19, no. 21 (2017): 5768–71. <a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">https://doi.org/10.1021/acs.orglett.7b02701</a>."},"page":"5768-5771","publisher":"American Chemical Society (ACS)","_id":"37972","user_id":"89271","volume":19,"status":"public","date_created":"2023-01-22T20:57:15Z","type":"journal_article","keyword":["CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"issue":"21","publication":"Organic Letters","extern":"1","language":[{"iso":"eng"}],"doi":"10.1021/acs.orglett.7b02701","title":"B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds","year":"2017","publication_identifier":{"issn":["1523-7060","1523-7052"]},"author":[{"full_name":"Li, Wu","last_name":"Li","first_name":"Wu"},{"first_name":"Ming-Ming","last_name":"Wang","full_name":"Wang, Ming-Ming"},{"full_name":"Hu, Yuya","last_name":"Hu","first_name":"Yuya"},{"full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","id":"89271"}],"publication_status":"published","date_updated":"2025-11-10T09:18:33Z","intvolume":"        19"},{"date_updated":"2025-11-10T09:28:45Z","publication_status":"published","intvolume":"        17","title":"First Base-Free Catalytic Wittig Reaction","year":"2015","author":[{"last_name":"Schirmer","first_name":"Marie-Luis","full_name":"Schirmer, Marie-Luis"},{"full_name":"Adomeit, Sven","first_name":"Sven","last_name":"Adomeit"},{"id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas","full_name":"Werner, Thomas"}],"publication_identifier":{"issn":["1523-7060","1523-7052"]},"doi":"10.1021/acs.orglett.5b01352","language":[{"iso":"eng"}],"extern":"1","publication":"Organic Letters","issue":"12","type":"journal_article","keyword":["T2","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T21:07:30Z","status":"public","user_id":"89271","volume":17,"page":"3078-3081","publisher":"American Chemical Society (ACS)","_id":"37995","citation":{"ieee":"M.-L. Schirmer, S. Adomeit, and T. Werner, “First Base-Free Catalytic Wittig Reaction,” <i>Organic Letters</i>, vol. 17, no. 12, pp. 3078–3081, 2015, doi: <a href=\"https://doi.org/10.1021/acs.orglett.5b01352\">10.1021/acs.orglett.5b01352</a>.","apa":"Schirmer, M.-L., Adomeit, S., &#38; Werner, T. (2015). First Base-Free Catalytic Wittig Reaction. <i>Organic Letters</i>, <i>17</i>(12), 3078–3081. <a href=\"https://doi.org/10.1021/acs.orglett.5b01352\">https://doi.org/10.1021/acs.orglett.5b01352</a>","mla":"Schirmer, Marie-Luis, et al. “First Base-Free Catalytic Wittig Reaction.” <i>Organic Letters</i>, vol. 17, no. 12, American Chemical Society (ACS), 2015, pp. 3078–81, doi:<a href=\"https://doi.org/10.1021/acs.orglett.5b01352\">10.1021/acs.orglett.5b01352</a>.","bibtex":"@article{Schirmer_Adomeit_Werner_2015, title={First Base-Free Catalytic Wittig Reaction}, volume={17}, DOI={<a href=\"https://doi.org/10.1021/acs.orglett.5b01352\">10.1021/acs.orglett.5b01352</a>}, number={12}, journal={Organic Letters}, publisher={American Chemical Society (ACS)}, author={Schirmer, Marie-Luis and Adomeit, Sven and Werner, Thomas}, year={2015}, pages={3078–3081} }","chicago":"Schirmer, Marie-Luis, Sven Adomeit, and Thomas Werner. “First Base-Free Catalytic Wittig Reaction.” <i>Organic Letters</i> 17, no. 12 (2015): 3078–81. <a href=\"https://doi.org/10.1021/acs.orglett.5b01352\">https://doi.org/10.1021/acs.orglett.5b01352</a>.","ama":"Schirmer M-L, Adomeit S, Werner T. First Base-Free Catalytic Wittig Reaction. <i>Organic Letters</i>. 2015;17(12):3078-3081. doi:<a href=\"https://doi.org/10.1021/acs.orglett.5b01352\">10.1021/acs.orglett.5b01352</a>","short":"M.-L. Schirmer, S. Adomeit, T. Werner, Organic Letters 17 (2015) 3078–3081."}}]
