---
_id: '62095'
author:
- first_name: Jan
  full_name: Tönjes, Jan
  last_name: Tönjes
- first_name: Lukas
  full_name: Kell, Lukas
  last_name: Kell
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
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>
  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}
    }'
  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>.'
  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.
date_created: 2025-11-05T15:22:44Z
date_updated: 2025-11-10T08:46:39Z
department:
- _id: '35'
- _id: '2'
doi: 10.1021/acs.orglett.3c03463
intvolume: '        25'
issue: '51'
keyword:
- T2
- CSSD
language:
- iso: eng
page: 9114-9118
publication: Organic Letters
publication_identifier:
  issn:
  - 1523-7060
  - 1523-7052
publication_status: published
publisher: American Chemical Society (ACS)
status: public
title: Organocatalytic Stereospecific Appel Reaction
type: journal_article
user_id: '89271'
volume: 25
year: '2023'
...
---
_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. <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>
  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} }'
  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>.
  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>.'
  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>.
  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: '37976'
author:
- first_name: Wu
  full_name: Li, Wu
  last_name: Li
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
citation:
  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>'
  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} }'
  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>.'
  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.
date_created: 2023-01-22T20:59:34Z
date_updated: 2025-11-10T09:14:45Z
department:
- _id: '35'
- _id: '2'
- _id: '657'
doi: 10.1021/acs.orglett.7b00720
extern: '1'
intvolume: '        19'
issue: '10'
keyword:
- CSSD
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: '89271'
volume: 19
year: '2017'
...
---
_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
  orcid: 0000-0001-9025-3244
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>
  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>
  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} }'
  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>.'
  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>.
  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: 2025-11-10T09:18:33Z
department:
- _id: '35'
- _id: '2'
- _id: '657'
doi: 10.1021/acs.orglett.7b02701
extern: '1'
intvolume: '        19'
issue: '21'
keyword:
- CSSD
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(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration
  of Electron-Rich Aromatic and Heteroaromatic Compounds
type: journal_article
user_id: '89271'
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
  orcid: 0000-0001-9025-3244
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>
  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>
  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>.'
  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>.'
  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>.
  short: M.-L. Schirmer, S. Adomeit, T. Werner, Organic Letters 17 (2015) 3078–3081.
date_created: 2023-01-22T21:07:30Z
date_updated: 2025-11-10T09:28:45Z
department:
- _id: '35'
- _id: '2'
- _id: '657'
doi: 10.1021/acs.orglett.5b01352
extern: '1'
intvolume: '        17'
issue: '12'
keyword:
- T2
- CSSD
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: '89271'
volume: 17
year: '2015'
...