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Hou, Chuanqi, Chen, Pinhong, Liu, Guosheng (2020) Enantioselective Palladium(II)‐Catalyzed Oxidative Aminofluorination of Unactivated Alkenes with Et 4 NF⋅3 HF as a Fluoride Source. Angewandte Chemie International Edition, 59 (7). 2735-2739 doi:10.1002/anie.201913100

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Reference TypeJournal (article/letter/editorial)
TitleEnantioselective Palladium(II)‐Catalyzed Oxidative Aminofluorination of Unactivated Alkenes with Et 4 NF⋅3 HF as a Fluoride Source
JournalAngewandte Chemie International Edition
AuthorsHou, ChuanqiAuthor
Chen, PinhongAuthor
Liu, GuoshengAuthor
Year2020 (February 10)Volume59
Issue7
PublisherWiley
DOIdoi:10.1002/anie.201913100Search in ResearchGate
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Mindat Ref. ID8656366Long-form Identifiermindat:1:5:8656366:8
GUID0
Full ReferenceHou, Chuanqi, Chen, Pinhong, Liu, Guosheng (2020) Enantioselective Palladium(II)‐Catalyzed Oxidative Aminofluorination of Unactivated Alkenes with Et 4 NF⋅3 HF as a Fluoride Source. Angewandte Chemie International Edition, 59 (7). 2735-2739 doi:10.1002/anie.201913100
Plain TextHou, Chuanqi, Chen, Pinhong, Liu, Guosheng (2020) Enantioselective Palladium(II)‐Catalyzed Oxidative Aminofluorination of Unactivated Alkenes with Et 4 NF⋅3 HF as a Fluoride Source. Angewandte Chemie International Edition, 59 (7). 2735-2739 doi:10.1002/anie.201913100
In(2020, February) Angewandte Chemie International Edition Vol. 59 (7) Wiley

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Hou, Chuanqi, Chen, Pinhong, Liu, Guosheng (2020) Enantioselective Palladium(II)‐Catalyzed Oxidative Aminofluorination of Unactivated Alkenes with Et 4 NF⋅3 HF as a Fluoride Source. Angewandte Chemie, 132 (7). 2757-2761 doi:10.1002/ange.201913100
Li, Xiaonan, Qi, Xiaoxu, Hou, Chuanqi, Chen, Pinhong, Liu, Guosheng (2020) Palladium(II)‐Catalyzed Enantioselective Azidation of Unactivated Alkenes. Angewandte Chemie International Edition, 59 (39) 17239-17244 doi:10.1002/anie.202006757
Li, Xiaonan, Qi, Xiaoxu, Hou, Chuanqi, Chen, Pinhong, Liu, Guosheng (2020) Palladium(II)‐Catalyzed Enantioselective Azidation of Unactivated Alkenes. Angewandte Chemie, 132 (39) 17392-17397 doi:10.1002/ange.202006757
Chen, Chaohuang, Pflüger, Philipp Miro, Chen, Pinhong, Liu, Guosheng (2019) Palladium(II)‐Catalyzed Enantioselective Aminotrifluoromethoxylation of Unactivated Alkenes using CsOCF 3 as a Trifluoromethoxide Source. Angewandte Chemie International Edition, 58 (8). 2392-2396 doi:10.1002/anie.201813591
Chen, Chaohuang, Pflüger, Philipp Miro, Chen, Pinhong, Liu, Guosheng (2019) Palladium(II)-Catalyzed Enantioselective Aminotrifluoromethoxylation of Unactivated Alkenes using CsOCF3 as a Trifluoromethoxide Source. Angewandte Chemie, 131 (8). 2414-2418 doi:10.1002/ange.201813591
Qi, Xiaoxu, Yu, Feng, Chen, Pinhong, Liu, Guosheng (2017) Intermolecular Palladium-Catalyzed Oxidative Fluorocarbonylation of Unactivated Alkenes: Efficient Access to β-Fluorocarboxylic Esters. Angewandte Chemie International Edition, 56 (41). 12692-12696 doi:10.1002/anie.201706401
Wu, Tao, Cheng, Jiashun, Chen, Pinhong, Liu, Guosheng (2013) Regioselective palladium-catalyzed intramolecular oxidative aminofluorination of unactivated alkenes. Chemical Communications, 49 (77). 8707pp. doi:10.1039/c3cc44711a
Li, Xiang, Chen, Pinhong, Liu, Guosheng (2018) Palladium-Catalyzed Intermolecular Arylcarbonylation of Unactivated Alkenes: Incorporation of Bulky Aryl Groups at Room Temperature. Angewandte Chemie International Edition, 57 (48). 15871-15876 doi:10.1002/anie.201810405
Zhang, Wen, Chen, Pinhong, Liu, Guosheng (2017) Enantioselective Palladium(II)-Catalyzed Intramolecular Aminoarylation of Alkenes by Dual N−H and Aryl C−H Bond Cleavage. Angewandte Chemie International Edition, 56 (19). 5336-5340 doi:10.1002/anie.201700889
Qi, Xiaoxu, Chen, Chaohuang, Hou, Chuanqi, Fu, Liang, Chen, Pinhong, Liu, Guosheng (2018) Enantioselective Pd(II)-Catalyzed Intramolecular Oxidative 6-endo Aminoacetoxylation of Unactivated Alkenes. Journal Of The American Chemical Society, 140 (24) 7415-7419 doi:10.1021/jacs.8b03767
Yang, Xintuo, Chen, Pinhong, Liu, Guosheng (2024) Asymmetric 1,n‐Remote Aminoacetoxylation of Unactivated Internal Alkenes Enabled by Palladium Catalysis. Angewandte Chemie International Edition, 63 (35) doi:10.1002/anie.202408305
 
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