22. Zhao, Y.; Wang, X.（本科生）; Liu, X.;* Cheng, Q.* Modular Assembly of Cyclic Sulfones via Radical Annulation with Unactivated Olefins. Eur. J. Org. Chem. 2025, 10.1002/ejoc.202501044. (Special Collection “Enlightening the Future: Synthesis and Applications in Photochemistry” on the occasion of ICPI 2025: International Conference on Photochemistry and Industry)
21. Zhang, J.;# Wu, G.;# Zhao, Y.; Liu, X.; Zhu, H.; Studer, A.; Qi, X.;* Cheng, Q.* "Spin-density-controlled radical coupling for meta-selective C–H halogenation of pyridines." Nat. Synth. 2025, 10.1038/s44160-025-00869-6. (# equal contribution)
19. Haring M.; Balanna, K., Cheng, Q., Lammert, J., Studer A.* "Formal meta-C-H Fluorination of Pyridines and Isoquinolines through Dearomatized Oxazinopyridine Intermediates." J. Am. Chem. Soc. 2024, 146, 30758–30763.
18. Zhang, J.; Wang, J.; Cheng, Q.* "Recent advances in C–F bond formation from carbon-centered radicals." Chin. J. Chem. 2024, 42, 1009-1031.
17. Cheng, Q.;# Bhattacharya, D.;# Haring, M.; Cao, H.; Mück-Lichtenfeld, C.; Studer, A.* “Skeletal Editing of Pyridines through Atom Pair Swap from CN to CC.” Nat. Chem. 2024, 16, 741–748. (#equal contribution)
16. Cao, H.;# Cheng, Q.;# Studer, A.* “Radical and ionic meta-C–H functionalization of pyridines, quinolines, and isoquinolines.” Science 2022, 378, 779–785. (#equal contribution)
15. Cheng, Q.; Bai, Z.; Tewari, S.; Ritter, T.* “Bifunctional Sulfilimines Enable Synthesis of Multiple N-Heterocycles from Alkenes.” Nat. Chem. 2022, 14, 898–904.
14. Cheng, Q.; Chen, J.; Lin, S.; Ritter, T.* “Allylic Amination of Alkenes with Iminothianthrenes to Afford Alkyl Allylamines.” J. Am. Chem. Soc. 2020, 142, 17287–17293.
13. Cheng, Q.; Ritter, T.* “New Directions in C–H Fluorination.” Trends Chem. 2019, 1, 461–470.
12. Cheng, Q.; Xie, J.-H.; Weng, Y.-C.; You, S.-L.* “Pd-Catalyzed Dearomatization Reaction of Anthranils with Vinylcyclopropanes via [4+3] Cyclization Reaction.” Angew. Chem. Int. Ed. 2019, 58, 5739–5743.
11. Cheng, Q.;# Tu, H.-F.;# Zheng, C.; Qu, J.-P.; Helmchen, G.; You, S.-L.* “Iridium-Catalyzed Asymmetric Allylic Substitution Reactions.” Chem. Rev. 2019, 119, 1855–1969. (# equal contribution)
10. Cheng, Q.; Zhang, F.; Cai, Y.; Guo, Y.-L.*; You, S.-L.* "Stereodivergent Synthesis of Tetrahydrofuroindoles via Palladium-Catalyzed Asymmetric Dearomative Formal [3+2] Cycloaddition Reactions." Angew. Chem. Int. Ed. 2018, 57, 2134–2138.
9. Cheng, Q.; Zhang, H.-J.; Yue, W.-J.; You, S.-L.* "Palladium-Catalyzed Highly Stereoselective Dearomative [3+2] Cycloaddition of Nitrobenzofurans." Chem 2017, 3, 428–436.
8. Cheng, Q.* "Natural-Product-Inspired Dearomatization of Nitrobenzofurans." Chem 2017, 3, 380–382.
7. Cheng, Q.; Wang, Y.; You, S.-L.* "Chemo-, Diastereo- and Enantioselective Iridium-Catalyzed Allylic Intramolecular Dearomatization Reaction of Naphthol Derivatives." Angew. Chem. Int. Ed. 2016, 55, 3496–3499.
6. Cao, H.; Bhattacharya, D.; Cheng, Q.; Studer, A.* “ C–H Functionalization of Pyridines via Oxazino Pyridine Intermediates: Switching to para-Selectivity under Acidic Conditions.” J. Am. Chem. Soc. 2023, 145, 15581–15588.
5. Cao, H.; Cheng, Q.; Studer, A.* “meta-Selective C−H Functionalization of Pyridines.” Angew. Chem. Int. Ed. 2023, 62, e202302941.
4. Ye, K.-Y.; Cheng, Q.; Zhuo, C.-X.; Dai, L.-X.; You, S.-L.* "Iridium(I) N-Heterocyclic Carbene Complex Catalyzed Asymmetric Intramolecular Allylic Amination Reactions." Angew. Chem. Int. Ed. 2016, 55, 8113–8116.
3. Zhang, X.; Liu, W.-B.; Cheng, Q.; You, S.-L.* "Iridium-Catalyzed Asymmetric Allylic Amination Reactions with N-Aryl Phosphoramidite Ligands." Organometallics 2016, 35, 2467–2472.
2. Zhuo, C.-X.; Cheng, Q.; Liu, W.-B.; Zhao, Q.; You, S.-L.* "Enantioselective Construction of Spiroindolines with Three Contiguous Stereogenic Centers and Chiral Tryptamine Derivatives via Reactive Spiroindolenine Intermediates." Angew. Chem. Int. Ed. 2015, 54, 14146–14149.
1. Zhuo, C.-X.; Zhou, Y.; Cheng, Q.; Huang, L.; You, S.-L.* "Enantioselective Synthesis of Pyrrole-Based Spiro- and Polycyclic Derivatives by Iridium-Catalyzed Asymmetric Allylic Dearomatization and Controllable Migration Reactions." Angew. Chem. Int. Ed. 2015, 54, 8475–8479.
