Zhi Zhou
Affiliations: | 2011-2016 | SIOC,CAS |
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| Chen W, Xu H, Liu FX, et al. (2024) Chiral Osmium(II)/Salox Species Enabled Enantioselective γ-C(sp3)-H Amidation: Integrated Experimental and Computational Validation For the Ligand Design and Reaction Development. Angewandte Chemie (International Ed. in English). e202401498 |
| Wu M, Wang Y, Zhou J, et al. (2023) Synthesis of Polysubstituted Furan Frameworks via [3 + 2] Annulation of -Enoxyimides with Chelated Alkynes Initiated by Rh(III)-Catalyzed C-H Activation. Organic Letters |
| Wu M, Zhang H, Wang T, et al. (2022) Rh(III)-Catalyzed chemo-, regio- and stereoselective carboamination of sulfonyl allenes with -phenoxy amides or -enoxy imides. Chemical Communications (Cambridge, England) |
| Zhang H, Lin S, Gao H, et al. (2021) Chemodivergent assembly of ortho-functionalized phenols with tunable selectivity via rhodium(III)-catalyzed and solvent-controlled C-H activation. Communications Chemistry. 4: 81 |
| Chen F, Tang J, Wei Y, et al. (2021) Rh(III)-Catalyzed and synergistic dual directing group-enabled redox-neutral [3+3] annulation of -phenoxyacetamides with α-allenols. Chemical Communications (Cambridge, England). 57: 9284-9287 |
| Xu H, Bian M, Zhou Z, et al. (2021) Mechanistic Insights into the Dual Directing Group-Mediated C-H Functionalization/Annulation a Hydroxyl Group-Assisted M-M-M Pathway. Acs Omega. 6: 17642-17650 |
| Yang J, Shi W, Chen W, et al. (2021) Rh(III)-Catalyzed Chemoselective C-H Alkenylation and [5 + 1] Annulation with -Difluoromethylene Enabled by the Distinctive Fluorine Effect. The Journal of Organic Chemistry |
| Wu L, Li L, Zhang H, et al. (2021) Rh(III)-Catalyzed C-H Activation/[3 + 2] Annulation of -Phenoxyacetamides via Carbooxygenation of 1,3-Dienes. Organic Letters |
| Zhong X, Lin S, Gao H, et al. (2021) Rh(III)-Catalyzed Redox-Neutral C-H Activation/[3 + 2] Annulation of -Phenoxy Amides with Propargylic Monofluoroalkynes. Organic Letters |
| Bian M, Mawjuda H, Gao H, et al. (2020) Lossen Rearrangement vs C-N Reductive Elimination Enabled by Rh(III)-Catalyzed C-H Activation/Selective Lactone Ring-Opening: Chemodivergent Synthesis of Quinolinones and Dihydroisoquinolinones. Organic Letters |