Before NJU
1. Y.-B. Li†, F.-P. Wu†, J. Tyler, C. G. Daniliuc, F. Glorius*, Substituent-rebound skeletal editing for precise boron-to-carbon single-atom swapping. (submitted) (†equal first author)
2. F.-P. Wu†, J. Tyler†, F. Glorius*, Diversity-Generating Skeletal Editing Transformations. Acc. Chem. Res.2025, 58, 893-906. (†equal first author)
3. F.-P. Wu, C. C. Chintawar, R. Lalisse, P. Mukherjee, S. Dutta, J. Tyler, C. G. Daniliuc, O. Gutierrez*, F. Glorius*, Ring Expansion of Indene by Photoredox-Enabled Functionalized Carbon-Atom Insertion, Nat. Catal. 2024, 7, 242–251.
4. F.-P. Wu, M. Lenz, A. Suresh, A. R. Gogoi, J. Tyler, C. G. Daniliuc, O. Gutierrez*, F. Glorius*, Nitrogen-to-functionalized carbon atom transmutation of pyridine. Chem. Sci. 2024, 15, 15205−15211.
5. F.-P. Wu, J. Tyler, C. G. Daniliuc, F. Glorius*, Atomic Carbon Equivalent: Design and Application to Diversity-Generating Skeletal Editing from Indoles to 3‑Functionalized Quinolines. ACS Catal. 2024, 14, 13343−13351.
6. F.-P. Wu, X.-W. Gu, H.-Q. Geng, X.-F. Wu*, Copper-catalyzed defluorinative arylboration of vinylarenes with polyfluoroarenes. Chem. Sci. 2023, 14, 2342-2347.
7. F.-P. Wu, H.-Qi. Geng, X.-F. Wu*, Copper-Catalyzed Boroaminomethylation of Olefins to γ-Boryl Amines with CO as C1 Source. Angew. Chem. Int. Ed. 2022, 61, e202211455.
8. F.-P. Wu, Y. Yang, D. P. Fuentes, X.-F. Wu*, Copper-Catalyzed Carbonylative Catenation of Olefins: Direct Synthesis of γ-Boryl Esters. Chem 2022, 7, 1982-1992.
9. F.-P. Wu, X.-F. Wu, Catalyst-Controlled Selective Borocarbonylation of Benzylidenecyclopropanes: Regiodivergent Synthesis of γ-Vinylboryl Ketones and β-Cyclopropylboryl Ketones. Chem. Sci. 2022, 13, 4321-4326.
10. F.-P. Wu, X.-F. Wu*, Ligand-Controlled Copper-Catalyzed Regiodivergent Carbonylative Synthesis of α-Amino Ketones and α-Boryl Amides from Imines and Alkyl Iodides. Angew. Chem. Int. Ed. 2021, 60, 695-700.
11. F.-P. Wu, Y. Yuan, J. Liu, X.-F. Wu*, Pd/Cu-Catalyzed Defluorinative Carbonylative Coupling of Aryl Iodides and gem-Difluoroalkenes: Efficient Synthesis of α-Fluorochalcones. Angew. Chem. Int. Ed. 2021, 60, 8818-8822.
12. F.-P. Wu, X.-F. Wu*, Copper-Catalyzed Borylative Methylation of Alkyl Iodides with CO as the C1 Source: Advantaged by Faster Reaction of CuH over CuBpin. Angew. Chem. Int. Ed. 2021, 60, 11730-11734.
13. F.-P. Wu, Y. Yuan, X.-F. Wu*, Copper-Catalyzed 1,2-Trifluoromethylation Carbonylation of Unactivated Alkenes: Efficient Access to β-Trifluoromethylated Aliphatic Carboxylic Acid Derivatives. Angew. Chem. Int. Ed. 2021, 60, 25787-25792.
14. F.-P. Wu, X.-F. Wu*, Pd/Cu-Catalyzed Amide-Enabled Selectivity-Reversed Borocarbonylation of Unactivated Alkenes. Chem. Sci. 2021, 12, 10341-10346.
15. F.-P. Wu, Y. Yuan, C. Schünemann, P. C. J. Kamer, X.-F. Wu*, Copper-Catalyzed Regioselective Borocarbonylative Coupling of Unactivated Alkenes with Alkyl Halides: Synthesis of β-Boryl Ketones. Angew. Chem. Int. Ed. 2020, 59, 10451-10455.
16. F.-P. Wu, X. Luo, U. Radius, T. B. Marder*, X.-F. Wu*, Copper-Catalyzed Synthesis of Stereodefined Cyclopropyl Bis(boronates) from Alkenes with CO as the C1 Source. J. Am. Chem. Soc. 2020, 142, 14074-14079.
17. F.-P. Wu, J. Holz, Y. Yuan, X.-F. Wu*, Copper-Catalyzed Carbonylative Synthesis of β-Boryl Amides via Boroamidation of Alkenes. CCS Chem. 2020, 2, 2643-2654.
18. F.-P. Wu, D. Li, J.-B. Peng, X.-F. Wu*, Carbonylative Transformation of Allylarenes with CO Surrogates: Tunable Synthesis of 4-Arylbutanoic Acids, 2-Arylbutanoic Acids, and 4-Arylbutanals. Org. Lett. 2019, 21, 5699-5703.
19. F.-P. Wu, J.-B. Peng, X. Qi, J. Ying, X.-F. Wu*, Palladium-Catalyzed Solvent-Dependent Divergent Synthesis of Benzylformamides. Adv. Synth. Catal. 2018, 360, 3412-3417.
20. F.-P. Wu, J.-B. Peng, L.-S. Meng, X. Qi, X.-F. Wu*, Palladium-Catalyzed Ligand-Controlled Selective Synthesis of Aldehydes and Acids from Aryl Halides and Formic Acid, ChemCatChem 2017, 9,3121-3124.
21. F.-P. Wu, J.-B. Peng, L.-Y. Fu, X. Qi, X.-F. Wu*, Direct Palladium-Catalyzed Carbonylative Transformation of Allylic Alcohols and Related Derivatives. Org. Lett. 2017, 19, 5474-5477.