[{"title":"Organocatalytic Stereospecific Appel Reaction","doi":"10.1021/acs.orglett.3c03463","publisher":"American Chemical Society (ACS)","date_updated":"2025-11-10T08:46:39Z","author":[{"first_name":"Jan","full_name":"Tönjes, Jan","last_name":"Tönjes"},{"last_name":"Kell","full_name":"Kell, Lukas","first_name":"Lukas"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner"}],"date_created":"2025-11-05T15:22:44Z","volume":25,"year":"2023","citation":{"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>","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>.","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>.","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} }","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>.","short":"J. Tönjes, L. Kell, T. Werner, Organic Letters 25 (2023) 9114–9118.","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>"},"page":"9114-9118","intvolume":"        25","publication_status":"published","publication_identifier":{"issn":["1523-7060","1523-7052"]},"issue":"51","keyword":["T2","CSSD"],"language":[{"iso":"eng"}],"_id":"62095","user_id":"89271","department":[{"_id":"35"},{"_id":"2"}],"status":"public","type":"journal_article","publication":"Organic Letters"},{"status":"public","publication":"Organic Letters","type":"journal_article","language":[{"iso":"eng"}],"_id":"22232","user_id":"53339","year":"2021","page":"3626-3630","citation":{"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>.","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>.","short":"G. Wicker, R. Schoch, J. Paradies, Organic Letters (2021) 3626–3630.","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} }","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>"},"publication_identifier":{"issn":["1523-7060","1523-7052"]},"publication_status":"published","title":"Diastereoselective Synthesis of Dihydro-quinolin-4-ones by a Borane-Catalyzed Redox-Neutral endo-1,7-Hydride Shift","doi":"10.1021/acs.orglett.1c01018","date_updated":"2023-01-23T12:57:10Z","author":[{"last_name":"Wicker","full_name":"Wicker, Garrit","first_name":"Garrit"},{"first_name":"Roland","full_name":"Schoch, Roland","last_name":"Schoch"},{"first_name":"Jan","full_name":"Paradies, Jan","id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X"}],"date_created":"2021-05-26T10:26:30Z"},{"keyword":["CSSD"],"language":[{"iso":"eng"}],"publication":"Organic Letters","publisher":"American Chemical Society (ACS)","date_created":"2023-01-22T20:59:34Z","title":"B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles","issue":"10","year":"2017","_id":"37976","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"extern":"1","type":"journal_article","status":"public","date_updated":"2025-11-10T09:14:45Z","author":[{"full_name":"Li, Wu","last_name":"Li","first_name":"Wu"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271","full_name":"Werner, Thomas"}],"volume":19,"doi":"10.1021/acs.orglett.7b00720","publication_status":"published","publication_identifier":{"issn":["1523-7060","1523-7052"]},"citation":{"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>","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} }","short":"W. Li, T. Werner, Organic Letters 19 (2017) 2568–2571.","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>.","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>.","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>"},"intvolume":"        19","page":"2568-2571"},{"year":"2017","intvolume":"        19","page":"5768-5771","citation":{"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>","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>.","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.","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} }"},"publication_identifier":{"issn":["1523-7060","1523-7052"]},"publication_status":"published","issue":"21","title":"B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds","doi":"10.1021/acs.orglett.7b02701","publisher":"American Chemical Society (ACS)","date_updated":"2025-11-10T09:18:33Z","volume":19,"author":[{"first_name":"Wu","last_name":"Li","full_name":"Li, Wu"},{"first_name":"Ming-Ming","full_name":"Wang, Ming-Ming","last_name":"Wang"},{"last_name":"Hu","full_name":"Hu, Yuya","first_name":"Yuya"},{"full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"date_created":"2023-01-22T20:57:15Z","status":"public","publication":"Organic Letters","type":"journal_article","keyword":["CSSD"],"extern":"1","language":[{"iso":"eng"}],"_id":"37972","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271"},{"doi":"10.1021/acs.orglett.5b01352","title":"First Base-Free Catalytic Wittig Reaction","author":[{"last_name":"Schirmer","full_name":"Schirmer, Marie-Luis","first_name":"Marie-Luis"},{"last_name":"Adomeit","full_name":"Adomeit, Sven","first_name":"Sven"},{"orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"date_created":"2023-01-22T21:07:30Z","volume":17,"date_updated":"2025-11-10T09:28:45Z","publisher":"American Chemical Society (ACS)","citation":{"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>","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>.","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>.","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} }","short":"M.-L. Schirmer, S. Adomeit, T. Werner, Organic Letters 17 (2015) 3078–3081.","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>.","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>"},"page":"3078-3081","intvolume":"        17","year":"2015","issue":"12","publication_status":"published","publication_identifier":{"issn":["1523-7060","1523-7052"]},"extern":"1","language":[{"iso":"eng"}],"keyword":["T2","CSSD"],"user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37995","status":"public","type":"journal_article","publication":"Organic Letters"}]