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1. Yan, J.-L.; Wang, H.; Chi, Y. R. Asymmetric Carbene Catalysis. In Asymmetric Catalytic Synthesis (4th Edition); Akiyama, T. and Ojima, I. (Ed.), Wiley VCH, 2022, 199-242.£¨×¨ÖøÕ½ڣ©
2. Yan, J.-L.?; Maiti, R.?; Ren, S.-C.; Tian, W.; Li, T.; Xu, J.; Mondal, B.; Jin, Z.*; Chi, Y. R.* Carbene-Catalyzed Atroposelective Synthesis of Axially Chiral Styrenes. Nat. Commun. 2022, 13, 84.
3. Maiti, R. ?; Yan, J.-L. ?(ÅäºÏÒ»×÷); Yang, X.; Mondal, B.; Xu, J.; Chai, H. Jin, Z.; Chi, Y. R.* Carbene-Catalyzed catalyzed Asymmetric Hydrophosphination (AHP) of ¦Á-Bromoenals to Prepare Diarylalkyl and Trialkyl Phosphines. Angew. Chem. Int. Ed. 2021, 60, 26616-26621.
4. Yu, J. ?; Yan, J.-L. ?(ÅäºÏÒ»×÷); Wu, F.?, Yang, M. Guo, Y.; Ye, T.* The Second-Generation Synthesis of Psymberin. Org. Lett. 2025, manuscript in revision.
5. Yan, J.-L. ; Yu, J.; Cheng, Y.; Yang, M.; Xu, Z.; Ye, T.* Towards the Total Synthesis of Mandelalide B: Construction of the Tetrahydrofuran/¦Á-hydroxyl Lactone Fragment. Org. Chem. Front. 2024, 11, 6353-6357.
6. Yan, J.-L.; Cheng, Y.; Chen, J.; Ratnayake, R.; Dang, L. H.; Luesch, H.; Guo, Y.*; Ye, T.*, Total Synthesis of Asperphenins A and B. Org. Lett. 2018, 20, 6170-6173.
7. Yan, J.-L.; Nan, H.; Fang, X.; Long, X.; Jiang, Y; Liu, J.* The isolation, bioactivity, and synthesis of natural products from Litsea verticillate with anti-HIV activities. Front. Pharmacol. 2024, 15, 1477878.
8. He, Y.; Chen, J.; Jiang, Y.; Fang, X.; Liu, J.*; Yan, J.-L.* N©\Heterocyclic Carbene Catalyzed Reactions Involving Acetylenic Breslow and/or Acylazolium as Key Intermediates. Chem. Rec. 2024, e202400165.
9. Nan, H.; Long, X.-E.; He, J.; Xing, H.; Cheng, M.-J.; Peng, J.-B.; Ye, T.; Yan, J.-L.*; Liu, J.*, Total Synthesis of the Marine Cyclic Depsipeptide Lagunamide D. Marine Drugs 2025, 23, 99.
10. Liu, J.; Chen, H.; Wang, M.; He, W.; Yan, J.-L.* Organocatalytic asymmetric synthesis of P-stereogenic molecules. Front. Chem. 2023, 11, 1132025.
11. Wang, D.; Li, P.; Yan, J.-L.; Mao, H.; Liu, L.; Wang, M.; Chen, M.; Ye, T.; Chen, Y., Assigning the stereochemical structures of aurantinin A and B with the assistance of biosynthetic investigations. Org. Chem. Front. 2022, 9, 5949-5954.
12. Wang, F.-X.; Yan, J.-L.; Liu, Z.; Zhu, T.; Liu, Y.; Ren, S.-C.; Lv, W.-X.; Jin, Z.; Chi, Y. R.* Assembly of Multicyclic Isoquinoline Scaffolds from Pyridines: Formal Total Synthesis of Fredericamycin A. Chem. Sci. 2021, 12, 10259-10265.
13. Maiti, R.; Xu, J.; Yan, J.-L.; Mondal, B.; Yang, X.; Chai, H.*; Hao, L.; Jin, Z.; Chi, Y. R.*, Carbene-catalyzed selective addition of isothioureas to enals for access to sulphur-containing 5,6-dihyropyrimidin-4-ones. Org. Chem. Front. 2021, 8, 743-747.
14. Liang, X.; Luo, D.; Yan, J.-L.; Rezaei, M. A.; Salvador-Reyes, L. A.; Gunasekera, S. P.; Li, C.; Ye, T.; Paul, V. J.; Luesch, H.*, Discovery of Amantamide, a Selective CXCR7 Agonist from Marine Cyanobacteria. Org. Lett. 2019, 21, 1622-1626.
15. Lei, H.; Yan, J.; Yu, J; Liu, Y.; Wang, Z.; Xu, Z.*; Ye, T.*, Total Synthesis and Stereo-chemical Reassignment of Mandelalide A. Angew. Chem. Int. Ed. 2014, 53, 6533-6537.
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