Hong Yi
Affiliations: | 2017- | Technische Universität Berlin, Berlin, Berlin, Germany |
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Parents
Sign in to add mentorMartin Oestreich | post-doc | 2017-2019 | TU Berlin | |
(Alexander von Humboldt Fellow) |
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Publications
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Liang K, Zhang D, Su Y, et al. (2023) Fragile intermediate identification and reactivity elucidation in electrochemical oxidative α-C(sp)-H functionalization of tertiary amines. Chemical Science. 14: 4152-4157 |
Kranidiotis-Hisatomi N, Yi H, Oestreich M. (2021) Enantio- and Regioconvergent Nickel-Catalyzed C(sp3)-C(sp3) Cross-Coupling of Allylic Electrophiles Steered by a Silyl Group. Angewandte Chemie (International Ed. in English) |
Yi H, Oestreich M. (2019) Regiodivergent and Stereospecific Aziridine Opening by Copper-Catalyzed Addition of Silicon Grignard Reagents. Chemistry (Weinheim An Der Bergstrasse, Germany) |
Yi H, Mao W, Oestreich M. (2019) Enantioselective Construction of alpha-Chiral Silanes by Nickel-Catalyzed C(sp3)-C(sp3) Cross-Coupling. Angewandte Chemie (International Ed. in English) |
Yi H, Mao W, Oestreich M. (2019) Enantioselektiver Aufbau von α‐chiralen Silanen durch nickelkatalysierte C(sp 3 )‐C(sp 3 )‐Kreuzkupplung Angewandte Chemie. 131: 3613-3616 |
Yi H, Chen H, Bian C, et al. (2017) Coordination strategy-induced selective C-H amination of 8-aminoquinolines. Chemical Communications (Cambridge, England) |
Niu L, Yi H, Wang S, et al. (2017) Photo-induced oxidant-free oxidative C-H/N-H cross-coupling between arenes and azoles. Nature Communications. 8: 14226 |
Niu L, Liu J, Yi H, et al. (2017) Visible-Light-Induced External Oxidant-Free Oxidative Phosphonylation of C(sp2)–H Bonds Acs Catalysis. 7: 7412-7416 |
Yi H, Bian C, Hu X, et al. (2015) Visible light mediated efficient oxidative benzylic sp(3) C-H to ketone derivatives obtained under mild conditions using O2. Chemical Communications (Cambridge, England) |
Liu J, Zhang H, Yi H, et al. (2015) A facile access for the C-N bond formation by transition metal-free oxidative coupling of benzylic C-H bonds and amides Science China Chemistry |