--- _id: '22232' author: - first_name: Garrit full_name: Wicker, Garrit last_name: Wicker - 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 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. Organic Letters. Published online 2021:3626-3630. doi:10.1021/acs.orglett.1c01018 apa: Wicker, G., Schoch, R., & Paradies, J. (2021). Diastereoselective Synthesis of Dihydro-quinolin-4-ones by a Borane-Catalyzed Redox-Neutral endo-1,7-Hydride Shift. Organic Letters, 3626–3630. https://doi.org/10.1021/acs.orglett.1c01018 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={10.1021/acs.orglett.1c01018}, journal={Organic Letters}, author={Wicker, Garrit and Schoch, Roland and Paradies, Jan}, year={2021}, pages={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.” Organic Letters, 2021, 3626–30. https://doi.org/10.1021/acs.orglett.1c01018. 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,” Organic Letters, pp. 3626–3630, 2021, doi: 10.1021/acs.orglett.1c01018.' mla: Wicker, Garrit, et al. “Diastereoselective Synthesis of Dihydro-Quinolin-4-Ones by a Borane-Catalyzed Redox-Neutral Endo-1,7-Hydride Shift.” Organic Letters, 2021, pp. 3626–30, doi:10.1021/acs.orglett.1c01018. short: G. Wicker, R. Schoch, J. Paradies, Organic Letters (2021) 3626–3630. date_created: 2021-05-26T10:26:30Z date_updated: 2023-01-23T12:57:10Z doi: 10.1021/acs.orglett.1c01018 language: - iso: eng page: 3626-3630 publication: Organic Letters publication_identifier: issn: - 1523-7060 - 1523-7052 publication_status: published status: public title: Diastereoselective Synthesis of Dihydro-quinolin-4-ones by a Borane-Catalyzed Redox-Neutral endo-1,7-Hydride Shift type: journal_article user_id: '53339' year: '2021' ... --- _id: '37972' author: - first_name: Wu full_name: Li, Wu last_name: Li - first_name: Ming-Ming full_name: Wang, Ming-Ming last_name: Wang - first_name: Yuya full_name: Hu, Yuya last_name: Hu - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner citation: ama: Li W, Wang M-M, Hu Y, Werner T. B(C6F5)3-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds. Organic Letters. 2017;19(21):5768-5771. doi:10.1021/acs.orglett.7b02701 apa: Li, W., Wang, M.-M., Hu, Y., & Werner, T. (2017). B(C6F5)3-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds. Organic Letters, 19(21), 5768–5771. https://doi.org/10.1021/acs.orglett.7b02701 bibtex: '@article{Li_Wang_Hu_Werner_2017, title={B(C6F5)3-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds}, volume={19}, DOI={10.1021/acs.orglett.7b02701}, 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} }' chicago: 'Li, Wu, Ming-Ming Wang, Yuya Hu, and Thomas Werner. “B(C6F5)3-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds.” Organic Letters 19, no. 21 (2017): 5768–71. https://doi.org/10.1021/acs.orglett.7b02701.' ieee: 'W. Li, M.-M. Wang, Y. Hu, and T. Werner, “B(C6F5)3-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds,” Organic Letters, vol. 19, no. 21, pp. 5768–5771, 2017, doi: 10.1021/acs.orglett.7b02701.' mla: Li, Wu, et al. “B(C6F5)3-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds.” Organic Letters, vol. 19, no. 21, American Chemical Society (ACS), 2017, pp. 5768–71, doi:10.1021/acs.orglett.7b02701. short: W. Li, M.-M. Wang, Y. Hu, T. Werner, Organic Letters 19 (2017) 5768–5771. date_created: 2023-01-22T20:57:15Z date_updated: 2023-01-23T10:33:55Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1021/acs.orglett.7b02701 extern: '1' intvolume: ' 19' issue: '21' keyword: - Organic Chemistry - Physical and Theoretical Chemistry - Biochemistry language: - iso: eng page: 5768-5771 publication: Organic Letters publication_identifier: issn: - 1523-7060 - 1523-7052 publication_status: published publisher: American Chemical Society (ACS) status: public title: B(C6F5)3-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds type: journal_article user_id: '14931' volume: 19 year: '2017' ... --- _id: '37976' author: - first_name: Wu full_name: Li, Wu last_name: Li - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner citation: ama: 'Li W, Werner T. B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles. Organic Letters. 2017;19(10):2568-2571. doi:10.1021/acs.orglett.7b00720' apa: 'Li, W., & Werner, T. (2017). B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles. Organic Letters, 19(10), 2568–2571. https://doi.org/10.1021/acs.orglett.7b00720' bibtex: '@article{Li_Werner_2017, title={B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles}, volume={19}, DOI={10.1021/acs.orglett.7b00720}, number={10}, journal={Organic Letters}, publisher={American Chemical Society (ACS)}, author={Li, Wu and Werner, Thomas}, year={2017}, pages={2568–2571} }' chicago: 'Li, Wu, and Thomas Werner. “B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles.” Organic Letters 19, no. 10 (2017): 2568–71. https://doi.org/10.1021/acs.orglett.7b00720.' ieee: 'W. Li and T. Werner, “B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles,” Organic Letters, vol. 19, no. 10, pp. 2568–2571, 2017, doi: 10.1021/acs.orglett.7b00720.' mla: 'Li, Wu, and Thomas Werner. “B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles.” Organic Letters, vol. 19, no. 10, American Chemical Society (ACS), 2017, pp. 2568–71, doi:10.1021/acs.orglett.7b00720.' short: W. Li, T. Werner, Organic Letters 19 (2017) 2568–2571. date_created: 2023-01-22T20:59:34Z date_updated: 2023-01-23T10:32:35Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1021/acs.orglett.7b00720 extern: '1' intvolume: ' 19' issue: '10' keyword: - Organic Chemistry - Physical and Theoretical Chemistry - Biochemistry language: - iso: eng page: 2568-2571 publication: Organic Letters publication_identifier: issn: - 1523-7060 - 1523-7052 publication_status: published publisher: American Chemical Society (ACS) status: public title: 'B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles' type: journal_article user_id: '14931' volume: 19 year: '2017' ... --- _id: '37995' author: - first_name: Marie-Luis full_name: Schirmer, Marie-Luis last_name: Schirmer - first_name: Sven full_name: Adomeit, Sven last_name: Adomeit - first_name: Thomas full_name: Werner, Thomas id: '89271' last_name: Werner citation: ama: Schirmer M-L, Adomeit S, Werner T. First Base-Free Catalytic Wittig Reaction. Organic Letters. 2015;17(12):3078-3081. doi:10.1021/acs.orglett.5b01352 apa: Schirmer, M.-L., Adomeit, S., & Werner, T. (2015). First Base-Free Catalytic Wittig Reaction. Organic Letters, 17(12), 3078–3081. https://doi.org/10.1021/acs.orglett.5b01352 bibtex: '@article{Schirmer_Adomeit_Werner_2015, title={First Base-Free Catalytic Wittig Reaction}, volume={17}, DOI={10.1021/acs.orglett.5b01352}, 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.” Organic Letters 17, no. 12 (2015): 3078–81. https://doi.org/10.1021/acs.orglett.5b01352.' ieee: 'M.-L. Schirmer, S. Adomeit, and T. Werner, “First Base-Free Catalytic Wittig Reaction,” Organic Letters, vol. 17, no. 12, pp. 3078–3081, 2015, doi: 10.1021/acs.orglett.5b01352.' mla: Schirmer, Marie-Luis, et al. “First Base-Free Catalytic Wittig Reaction.” Organic Letters, vol. 17, no. 12, American Chemical Society (ACS), 2015, pp. 3078–81, doi:10.1021/acs.orglett.5b01352. short: M.-L. Schirmer, S. Adomeit, T. Werner, Organic Letters 17 (2015) 3078–3081. date_created: 2023-01-22T21:07:30Z date_updated: 2023-01-23T10:24:10Z department: - _id: '35' - _id: '2' - _id: '657' doi: 10.1021/acs.orglett.5b01352 extern: '1' intvolume: ' 17' issue: '12' keyword: - Organic Chemistry - Physical and Theoretical Chemistry - Biochemistry language: - iso: eng page: 3078-3081 publication: Organic Letters publication_identifier: issn: - 1523-7060 - 1523-7052 publication_status: published publisher: American Chemical Society (ACS) status: public title: First Base-Free Catalytic Wittig Reaction type: journal_article user_id: '14931' volume: 17 year: '2015' ...