Peer-reviewed publications (* means corresponding author. † means contributing equally)
26. Yong-Liang Su, Wei Xiong, Kaitlyn S. Otte, and Will R. Gutekunst* Photo-Triggerable Polymerization and Depolymerization of Stiff-Stilbene Lactones. J. Am. Chem. Soc. 2025, 147, 32054-32063.
25. Yong-Liang Su,† Liang Yue,† McKinley K. Paul, Joseph Kern, Kaitlyn S. Otte, Rampi Ramprasad, H. Jerry Qi,* and Will R. Gutekunst* Reprocessable and Recyclable Materials for 3D Printing via Reversible Thio-Michael Reaction. Angew. Chem. Int. Ed. 2025, 64, e202423522.
24. Joseph Kern, Yong-Liang Su, Will R. Gutekunst, Rampi Ramprasad* An Informatics Framework for the Design of Sustainable, Chemically Recyclable, Synthetically-Accessible and Durable Polymers. npj Computational Materials. 2025, 11, 182.
23. Kellie A. Stellmach, McKinley K. Paul, Yong-Liang Su, Anthony C. Engler,* and Will R. Gutekunst* Improving the Accuracy of Ceiling Temperature Measurements: Best Practices and Common Pitfalls. Macromolecules. 2025, 58, 3729-3741.
22. Yong-Liang Su, Wei Xiong, Liang Yue, Mckinley K. Paul, Kaitlyn S. Otte, John Bacsa, H. Jerry Qi, and Will R. Gutekunst* Michael Addition-Elimination Ring-Opening Polymerization. J. Am. Chem. Soc. 2024, 146, 18074-18082.
21. Liang Yue, Yong-Liang Su, Mingzhe Li, Luxia Yu, Xiaohao Sun, Jaehyun Cho, Blair Brettmann, Will R. Gutekunst, Rampi Ramprasad, H. Jerry Qi* Chemical Circularity in 3D Printing with Biobased Δ‐Valerolactone. Adv. Mater. 2024, 2310040.
20. Yong-Liang Su, Liang Yue, Huan Tran, Mizhi Xu, Anthony Engler, Rampi Ramprasad, H. Jerry Qi, and Will R. Gutekunst* Chemically Recyclable Polymer System Based on Nucleophilic Aromatic Ring-Opening Polymerization. J. Am. Chem. Soc. 2023, 145, 13950-13956.
19. Liang Yue, Yong-Liang Su, Mingzhe Li, Luxia Yu, S. Macrae Montgomery, Xiaohao Sun, M. G. Finn, Will R. Gutekunst, Rampi Ramprasad, and H. Jerry Qi* One-Pot Synthesis of Depolymerizable δ-Lactone Based Vitrimers. Adv. Mater. 2023, 23009534.
18. Yong-Liang Su,† Geng-Xin Liu†, Luca De Angelis†, Ru He, Ammar Al-Sayyed, Kirk S. Schanze, Wen-Hao Hu, Huang Qiu,* and Michael P. Doyle* Radical Cascade Multicomponent Minisci Reactions with Diazo Compounds. ACS Catal. 2022, 12, 1357-1363.
17. Yong-Liang Su, Michael P. Doyle* Application of α-Aminoalkyl Radicals as Reaction Activators. Synthesis, 2022, 54, 545-554.
16. Kellie A. Stellmach, McKinley K. Paul, Mizhi Xu, Yong-Liang Su, Liangbing Fu, Aubrey R. Toland, Huan Tran, Lihua Chen, Rampi Ramprasad* and Will R. Gutekunst* Modulating Polymerization Thermodynamics of Thiolactones Through Substituent and Heteroatom Incorporation. ACS Macro Lett. 2022, 11, 895-901.
15. Yong-Liang Su, Kuiyong Dong, Haifeng Zheng and Michael P. Doyle* Generation of Diazomethyl Radicals by Hydrogen Atom Abstraction and Their Cycloaddition with Alkenes. Angew. Chem. Int. Ed. 2021, 60, 18484-18488.
14. Siqi Liu, Yong-Liang Su, Tian-Yu Sun, Michael P. Doyle, * Yun-Dong Wu* and Xinhao Zhang* Precise Introduction of the −CHnX3−n (X = F, Cl, Br, I) Moiety to Target Molecules by a Radical Strategy: A Theoretical and Experimental Study. J. Am. Chem. Soc. 2021, 143, 13195-13204.
13. Kuiyong Dong, Haifeng Zheng, Yong-Liang Su, Ahmad Humeidi, Hadi Arman, Xinfang Xu,* and Michael P. Doyle* Catalyst-Directed Divergent Catalytic Approaches to Expand Structural and Functional Scaffold Diversity via Metallo-Enolcarbene Intermediates. ACS Catal. 2021, 11, 4712-4721.
12. Luca De Angelis, Alexandra M. Crawford, Yong-Liang Su, Daniel Wherritt, Hadi Arman, and Michael P. Doyle* Catalyst-Free Formation of Nitrile Oxides and Their Further Transformations to Diverse Heterocycles. Org. Lett. 2021, 23, 925-929.
11. Yong-Liang Su,† Geng-Xin Liu,† Jun-Wen Liu, Linh Tram, Huang Qiu,* and Michael P. Doyle* Radical-Mediated Strategies for the Functionalization of Alkenes with Diazo Compounds. J. Am. Chem. Soc. 2020, 142, 13846-13855.
10. Yong-Liang Su, Linh Tram, Daniel Wherritt, Hadi Arman, Wendell P. Griffith, and Michael P. Doyle* α-Amino Radical-Mediated Diverse Difunctionalization of Alkenes: Construction of C-C, C-N and C-S Bonds. ACS Catal. 2020, 10, 13682-13687.
9. Yong-Liang Su,† Luca De Angelis,† Linh Tram, Yang Yu, and Michael P. Doyle* Catalytic Oxidative Cleavage Reactions of Arylalkenes by tert-Butyl Hydroperoxide − A Mechanistic Assessment. J. Org. Chem. 2020, 85, 3728-3741.
8. Yong-Liang Su, Luca De Angelis, and Michael P. Doyle* Allylic Oxidation Catalyzed by Dirhodium(II) Tetrakis[Ɛ-caprolactamate] of tert-Butyldimethylsilyl-protected trans-Dehydroandrosterone. Org. Synth. 2019, 96, 300-311.
7. Robynne K. Neff,† Yong-Liang Su,† Siqi Liu, Melina Rosado, Xinhao Zhang, and Michael P. Doyle* Generation of Halomethyl Radicals by Halogen Atom Abstraction and Their Addition Reactions with Alkenes. J. Am. Chem. Soc. 2019, 141, 16643-16650.
6. Yong-Liang Su, Lu-Lu Li, Xiao-Le Zhou, Zhen-Yao Dai, Pu-Sheng Wang,* and Liu-Zhu Gong* Asymmetric α−Allylation of Aldehydes with Alkynes by Integrating Chiral Hydridopalladium and Enamine Catalysis. Org. Lett., 2018, 20, 2403–2406.
5. Lu-Lu Li, Yong-Liang Su, Zhi-Yong Han, and Liu-Zhu Gong* Assembly of Tetrahydropyran Derivatives from Aldehydes, Allylboronates, and Syngas by Asymmetric Relay Catalytic Cascade Reaction. Chem. Eur. J. 2018, 24, 7626-7630.
4. Zhou, Xiao-Le, Su, Yong-Liang, Wang, Pu-Sheng, Gong, Liu-Zhu* Asymmetric Allylic C-H Alkylation of 1,4-Dienes with Aldehydes. Acta Chim. Sinica 2018, 76, 857-861.
3. Yong-Liang Su,† Zhi-Yong Han,† Yu-Hui Li, and Liu-Zhu Gong* Asymmetric Allylation of Furfural Derivatives: Synergistic Effect of Chiral Ligand and Organocatalyst on Stereochemical Control. ACS Catal. 2017, 7, 7917−7922.
2. Yong-Liang Su, Yu-Hui Li, Yu-Gen Chen and Zhi-Yong Han* Ir/PTC Cooperatively Catalyzed Asymmetric Umpolung Allylation of a-Imino Ester Enabled Synthesis of a-Quaternary Amino Acid Derivatives Bearing Two Vicinal Stereocenters. Chem. Commun. 2017, 53, 1985-1988.
1. Yu-Ping He, Hua Wu, Lue Xu, Yong-Liang Su and Liu-Zhu Gong* Highly Enantioselective Oxidative Tandem Cyclization Reaction: a Chiral Ligand and an Anion Cooperatively Control Stereoselectivity. Org. Chem. Front. 2014, 1, 473-476.