Hua-Jie Jiang
Affiliations: | 2021- | Technische Universität Berlin, Berlin, Berlin, Germany |
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| Wu XB, Shen Y, Jiang HJ, et al. (2025) Cu-Catalyzed Enantioselective S-Arylation of Sulfenamides Enabled by Confined Ligands. Organic Letters. 27: 2845-2851 |
| Shen Y, Wu XB, Jiang HJ, et al. (2025) Anionic Stereogenic-at-Cobalt(III) Complex-Enabled Asymmetric Oxidation of ,-Dialkyl Sulfenamides. Organic Letters. 27: 2060-2064 |
| Fang YJ, Wu XB, Wang QM, et al. (2025) High-performance anionic stereogenic-at-cobalt(III) complex/halide salts/oxone catalytic system for enantioselective halocyclization of olefins. Chemical Communications (Cambridge, England) |
| Jiang HJ, Fang W, Chen X, et al. (2025) Unlocking Chiral Sulfinimidoyl Electrophiles: Asymmetric Synthesis of Sulfinamides Catalyzed by Anionic Stereogenic-at-Cobalt(III) Complexes. Journal of the American Chemical Society |
| Jiang HJ, Fang W, Meng YD, et al. (2024) Asymmetric S-Arylation of Sulfenamides to Access Axially Chiral Sulfilimines Enabled by Anionic Stereogenic-at-Cobalt(III) Complexes. Angewandte Chemie (International Ed. in English). e202419596 |
| Yao CZ, Tu XQ, Zhao ZY, et al. (2024) Enantioselective Organocatalyzed Cascade Dearomatizing Spirocycloaddition Reactions of Indole-Ynones. Organic Letters |
| Shen Y, Jiang HJ, Yu J, et al. (2024) Asymmetric Bromination/Semipinacol Rearrangement Enabled by Brønsted Acids of Stereogenic-at-Cobalt(III) Complexes. The Journal of Organic Chemistry |
| Fang W, Sun BB, Qin SC, et al. (2023) Enantioselective Access to Chiral 2,5-Diketopiperazines via Stereogenic-at-Cobalt(III)-Catalyzed Ugi-4CRs/Cyclization Sequences. The Journal of Organic Chemistry. 88: 16024-16037 |
| Zhu M, Jiang HJ, Sharanov I, et al. (2023) Atroposelective Silylation of 1,1'-Biaryl-2,6-diols by a Chiral Counteranion Directed Desymmetrization Enhanced by a Subsequent Kinetic Resolution. Angewandte Chemie (International Ed. in English). e202304475 |
| Wu X, Ding D, Zhang Y, et al. (2021) Enantioselective synthesis of 1-aminoindene derivatives asymmetric Brønsted acid catalysis. Chemical Communications (Cambridge, England) |