Diastereoselective Synthesis of Dihydro-quinolin-4-ones by a Borane-Catalyzed Redox-Neutral endo-1,7-Hydride Shift

G. Wicker, R. Schoch, J. Paradies, Organic Letters (2021) 3626–3630.

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Journal Article | Published | English
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Organic Letters
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3626-3630
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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. 2021:3626-3630. doi:10.1021/acs.orglett.1c01018
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
@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} }
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.
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.
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.

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