1. Liu, X. B.; Huang, Y.* “Recent advances in organic synthesis via synergistic nickel/copper catalysis” Coordin. Chem. Rev. 2023, 489, 215173.(IF: 20.6) Q1
2. Wei, L.-W.; Wang. Z.-Q; Wang, Z.; Zhao, Y.; Liu, S.*; Huang, Y.* Modular synthesis of polyfunctionalizaed axial-chiral 2-arylpyridines via asymmetric [2+2+2] cycloadditions using robust Cobalt Catalysst. Cell Rep. Phy. Sci. In revision(IF:8.9) Q1 (Cell 子刊)
3.Liu, X. B.; Wang, Z.; Yang, Y. ; Qu, K.*;Huang, Y.* “Amide and Peptide Synthesis via Ni-catalyzed Cross-electrophile Coupling. ” Cell Rep. Phy. Sci. (2024), https://doi.org/10.1016/j.xcrp.2024.102248(IF:8.9) Q1 (Cell 子刊)
4. Ren, X. L.; Qiao, Y. W.; Zhou, B. Q; Liu, S.*; Huang, Y.* “Nickel-catalzyed enantioselective migratory reductive cross-coupling enabled by radical 1,2-amino migration.” Revised.
5. Ma, Z.-C.; Wei, L.-W.; Liu, S.*; Huang, Y.* “Stereodivergent construction of [6.5]-spirocycles bearing three contiguous stereogenic centers by Pd-catalyzed [4+2] annulations.” Chem Catal. 2023, 3, 100669.(IF: 10.8) (Highlighted by Prof. Zhang Wanbin in Preview in Chem Catalysis, 2023, 3, 100673) "Emerging Investigator special collection" Q1
6. Qiao, Y.-W.; Zhou, B.-Q.; Huang, Y.* “Ni-catalyzed reductive alkygermylation of activated alkenes: modular access to polyfunctionalized alkyl germanes.” Chem Catal. 2023, 3, 100819.(IF: 10.8) (Highlighted by Prof. Alejandro Peraz-Luna in Preview in Chem Catalysis, 2023, 3, 100860) "Cover Article" "Emerging Investigator special collection" Q1
7. Ma, Z.-C.; Wei, L.-W.; Huang, Y.* “Stereodivergent Access to [6.7]-Fused N-Heterocycles Bearing 1,3-Nonadjacent Stereogenic Centers by Pd-Catalyzed [4+2] Annulations.” Org. Lett. 2023, 25, 1661-1666.(IF: 5.2) (*Highlighted by Prof. Mark Lautens in Synfact, 2023, 19, 0486) (*"SYNPACT" article invited by Prof. Peter C.Vollhardt 10.1055/a-2184-6373) Q1
8. Zi, P.-Z.; liu, X.-B.; Zhao, Q.-H.; He, M.; Huang, Y.* “1,6-Conjugate addition of para-quinone methides using gem-diborylcarbanions: Practical access to gem-diborylalkanes bearing vicinal tertiary/quaternary stereocenters. Green Syn. Catal. 2024, 5 , 68-72. (IF: 8.2) Q1
9. Zi, P.-Z.; Zhao, Q.-H.; Liu, S.*; Huang, Y.* “Transition metal-free Csp3-Csp3 bond-forming reactions of N-tosylaziridines and gem-diborylalkanes” Green Syn. Catal. 2024, In press, doi.org/10.1016/j.gresc. 2023.07.004. (IF:8.2) Q1
10. Huang, Y#; Ma. C#; Liu. S#; Yang. L-C; Lan, Y*.; Zhao, Y.* (#: equal contribution) “Ligand Coordination/Dissociation-Induced Divergent Allylic Alkylations Using Alkynes.” Chem 2021, 7, 812-826.(IF: 23.5) Q1
11. Huang, Y.; M. Kevin Brown*. “Synthesis of Bisheteroarylalkanes by Heteroarylboration: Development and Application of a Pyridylidene-Cu Complex.” Angew. Chem. Int. Ed. 2019, 58, 6048-6052. (IF: 16.6) Q1
12. Huang, Y.; Kevin, B. Smith.; M. Kevin Brown*. “Copper-Catalyzed Borylacylation of Activated Alkenes with Acid Chlorides.“ Angew. Chem. Int. Ed. 2017, 56, 13314-13318. (IF: 16.6) (Highlighted by Prof. Paul Knochel in Synfact, 2017,13,1309) Q1
13. Huang, Y.#; Huang. R-Z.#; Zhao, Y* (#: equal contribution) “Cobalt-Catalyzed Enantioselective Vinylation of Activated Ketones and Imines.” J. Am. Chem. Soc. 2016, 138, 6571-6577. (IF: 15.0) Q1
14. Huang, Y.; Ma, C.; Lee, Y. X.; Huang. R-Z.; Zhao, Y.* “Cobalt-Catalyzed Allylation of Heterobicyclic Alkenes: Ligand-Induced Divergent Reactivities.” Angew. Chem. Int. Ed. 2015, 54, 13696-13700. (IF: 16.6) (Highlighted by Prof. Mark Lautens in Synfact, 2015,11,1299) Q1
15. Ma, C.#; Huang, Y.#; Zhao, Y* (#: equal contribution). “Palladium-Catalyzed Enantioselective 1,6-Conjugate Addition/Annulation of para-Quinone Methides.” ACS Catalysis. 2016, 6, 6408-6412. (IF: 12.7) (Highlighted by Prof. Mark Lautens in Synfact, 2016, 12,1177) Q1
16. Huang, Y.; Yang, L-C.; Shao, P-L.; Zhao, Y*.“Practical, highly Stereroselective Allyl- and Crotysilylation of Aldehydes Catalyzed by Readily Available Cinchona Alkaloid Amide.” Chem. Sci. 2013, 4, 3275-3281. (IF: 8.4) Q1