| Diastereoselective Total Synthesis of (±)‐Schindilactone A Q Xiao, WW Ren, ZX Chen, TW Sun, Y Li, QD Ye, JX Gong, FK Meng, ... Angewandte Chemie 123 (32), 7511-7515, 2011 | 159 | 2011 |
| Efficient Synthesis of β-CF3/SCF3-Substituted Carbonyls via Copper-Catalyzed Electrophilic Ring-Opening Cross-Coupling of Cyclopropanols Y Li, Z Ye, TM Bellman, T Chi, M Dai Organic letters 17 (9), 2186-2189, 2015 | 141 | 2015 |
| Total synthesis of (−)-spinosyn A via carbonylative macrolactonization Y Bai, X Shen, Y Li, M Dai Journal of the American Chemical Society 138 (34), 10838-10841, 2016 | 106 | 2016 |
| Total Syntheses of the Reported Structures of Curcusone I and J via Tandem Gold Catalysis Y Li, M Dai Angewandte Chemie International Edition 56 (38), 11624-11627, 2017 | 63* | 2017 |
| Diastereoselective Total Synthesis of (±)‐Schindilactone A, Part 1: Construction of the ABC and FGH Ring Systems and Initial Attempts to Construct the CDEF Ring System TW Sun, WW Ren, Q Xiao, YF Tang, YD Zhang, Y Li, FK Meng, YF Liu, ... Chemistry–An Asian Journal 7 (10), 2321-2333, 2012 | 46 | 2012 |
| Diastereoselective Total Synthesis of (±)‐Schindilactone A, Part 3: The Final Phase and Completion WW Ren, ZX Chen, Q Xiao, Y Li, TW Sun, ZY Zhang, QD Ye, FK Meng, ... Chemistry–An Asian Journal 7 (10), 2341-2350, 2012 | 44 | 2012 |
| Biomimetically inspired asymmetric total synthesis of (+)-19-dehydroxyl arisandilactone A YX Han, YL Jiang, Y Li, HX Yu, BQ Tong, Z Niu, SJ Zhou, S Liu, Y Lan, ... Nature communications 8 (1), 14233, 2017 | 43 | 2017 |
| Diastereoselective Total Synthesis of (±)‐Schindilactone A, Part 2: Construction of the Fully Functionalized CDEFGH Ring System Y Li, ZX Chen, Q Xiao, QD Ye, TW Sun, FK Meng, WW Ren, L You, LM Xu, ... Chemistry–An Asian Journal 7 (10), 2334-2340, 2012 | 42 | 2012 |
| Asymmetric total synthesis of Pre-schisanartanin C YL Jiang, HX Yu, Y Li, P Qu, YX Han, JH Chen, Z Yang Journal of the American Chemical Society 142 (1), 573-580, 2019 | 35 | 2019 |
| Gold catalysis-facilitated rapid synthesis of the daphnane/tigliane tricyclic core Y Li, M Wei, M Dai Tetrahedron 73 (29), 4172-4177, 2017 | 34 | 2017 |
| Endosidin20 targets the cellulose synthase catalytic domain to inhibit cellulose biosynthesis L Huang, X Li, W Zhang, N Ung, N Liu, X Yin, Y Li, RE Mcewan, B Dilkes, ... The Plant Cell 32 (7), 2141-2157, 2020 | 32 | 2020 |
| Catalytic macrolactonizations for natural product synthesis Y Li, X Yin, M Dai Natural Product Reports 34 (10), 1185-1192, 2017 | 32 | 2017 |
| Endosidin2-14 targets the exocyst complex in plants and fungal pathogens to inhibit exocytosis L Huang, X Li, Y Li, X Yin, Y Li, B Wu, H Mo, CJ Liao, T Mengiste, W Guo, ... Plant physiology 180 (3), 1756-1770, 2019 | 15 | 2019 |
| Fused pyrazine derivatives as A2A/A2B inhibitors X Wang, Y Li, C Qi, L Wu, W Yao, W Zhu US Patent 11,161,850, 2021 | 13 | 2021 |
| Asymmetric total synthesis of Lancifodilactone G Acetate. 1. diastereoselective synthesis of CDEFGH ring system TW Sun, DD Liu, KY Wang, BQ Tong, JX Xie, YL Jiang, Y Li, B Zhang, ... The Journal of Organic Chemistry 83 (13), 6893-6906, 2018 | 11 | 2018 |
| Combination therapy comprising a2a/a2b inhibitors, pd-1/pd-l1 inhibitors, and anti-cd73 antibodies H Wang, JC Almagro, RA Buonpane, PN Carlsen, T Huang, Y Li, ... US Patent US20220233529A1, 2022 | | 2022 |
| Fused pyrazine derivatives as a2a/a2b inhibitors X Wang, PN Carlsen, P Gan, G Hoang, Y Li, C Qi, L Wu, W Yao, Z Yu, ... US Patent US20220135570A1, 2022 | | 2022 |
| Tricyclic compounds as inhibitors of KRAS X Wang, W Zhu, J Yang, A Sokolsky, C He, Z Li, C Qi, Y Li, P Gan, ... US Patent US20210269434A1, 2021 | | 2021 |
| Combination Therapy Comprising A2A/A2B and PD-1/PD-L1 Inhibitors H Wang, JC Almagro, RA Buonpane, PN Carlsen, T Huang, Y Li, L Lin, ... US Patent US20210205311A1, 2021 | | 2021 |
| Cd73 inhibitor and a2a/a2b adenosine receptor inhibitor combination therapy HG Nastri, SM Stewart, JC Almagro, J Zhou, RA Buonpane, H Wang, ... US Patent US20210230294A1, 2021 | | 2021 |
Mingji DaiProfessor of Chemistry, Purdue University在 purdue.edu 的电子邮件经过验证
