Selected publications

1. 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: 22.804)

2. 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: 15.336)

3. 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: 15.336)

4. 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: 15.419)

5. 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: 15.336)

6. 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: 13.084)

7. 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: 9.825)

8. Huang, Y.; Allison M. Bergmann, M. Kevin Brown* “(Hetero)arylboration of Alkynes: A Strategy for the Synthesis of α,α-Bis(hetero)arylketones.” Org. Biomol. Chem. 2019, 17, 5913-5915. (IF: 3.49)

9. Kevin, B. Smith.; Huang, Y.; M. Kevin Brown* “Copper-Catalyzed Heteroarylboration of Dienes: A Method for Direct Functionalization of Aromatic Nitrogen Containing Heterocycles.” Angew. Chem. Int. Ed. 2018, 57, 6146-6149. (IF: 15.336)

10. Lee, D.; Gao, Y.; Li, M.; Huang, Y.; Wang, J*. “Organocatalytic Azide-Enamine “Click” Reaction: Regiospecific Synthesis of 1, 4, 5-Trisubstituted-1, 2, 3-Triazoles.” Chem. Eur. J. 2011, 17, 3584-3587. (IF: 5.160)