---
_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'
...