Jiajia Ma
Affiliations: | Westfälische Wilhelms-Universität Münster, Münster, Nordrhein-Westfalen, Germany |
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Parents
Sign in to add mentorEric Meggers | grad student | 2014-2018 | University of Marburg |
Frank Glorius | post-doc | Westfälische Wilhelms-Universität Münster |
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Publications
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Liu DH, Nagashima K, Liang H, et al. (2023) Chemoselective Quinoline and Isoquinoline Reduction by Energy Transfer Catalysis Enabled Hydrogen Atom Transfer. Angewandte Chemie (International Ed. in English). e202312203 |
Guo R, Adak S, Bellotti P, et al. (2022) Photochemical Dearomative Cycloadditions of Quinolines and Alkenes: Scope and Mechanism Studies. Journal of the American Chemical Society |
Bellotti P, Rogge T, Paulus F, et al. (2022) Visible-Light Photocatalyzed -(3 + 2) Cycloadditions of Quinolines. Journal of the American Chemical Society |
Huang HM, Bellotti P, Ma J, et al. (2021) Bifunctional reagents in organic synthesis. Nature Reviews. Chemistry. 5: 301-321 |
Ma J, Chen S, Bellotti P, et al. (2021) Photochemical intermolecular dearomative cycloaddition of bicyclic azaarenes with alkenes. Science (New York, N.Y.). 371: 1338-1345 |
Ma J, Schäfers F, Daniliuc C, et al. (2020) Gadolinium Photocatalysis: Dearomative [2+2] Cycloaddition/Ring-Expansion Sequence with Indoles. Angewandte Chemie (International Ed. in English) |
Patra T, Mukherjee S, Ma J, et al. (2019) Visible-light photosensitized aryl and alkyl decarboxylative carbon-heteroatom and carbon-carbon bond formations. Angewandte Chemie (International Ed. in English) |
Ma J, Strieth-Kalthoff F, Dalton T, et al. (2019) Direct Dearomatization of Pyridines via an Energy-Transfer-Catalyzed Intramolecular [4+2] Cycloaddition Chem. 5: 2854-2864 |
Ma J, Lin J, Zhao L, et al. (2018) Synthesis of beta-Substituted gamma-Aminobutyric Acid Derivatives via Enantioselective Photoredox Catalysis. Angewandte Chemie (International Ed. in English) |
Ma J, Zhang X, Huang X, et al. (2018) Preparation of chiral-at-metal catalysts and their use in asymmetric photoredox chemistry. Nature Protocols. 13: 605-632 |