教育背景
承擔項目
吲哚生物鹼 Tabercarpamine A 和 Ervachinine C的全合成研究,2022.01-2024.12,30 萬,在研,主持。
工作經歷
2021.01-2024.12 中國科學院長春套用化學研究所綠色化學與過程實驗室 特別研究助理
2024.12-至今 中國科學院長春套用化學研究所綠色化學與過程實驗室 副研究員
研究方向
研究方向為具有重要生物活性的複雜天然產物全合成。碩士期間,開發了系列含有 1-羥基-3- 甲基片段的手性砌塊的高效合成方法,同時完成了海綿類天然產物 Fursopngin-1 和Dihydrofurospongin-2 對映體的合成工作。在攻博期間,建立了金雞納鹼季銨鹽手性催化劑催化吲哚衍生物與丙烯醛衍生物的不對稱 Michael/aldol 串聯反應,並以此方法為關鍵反應,成功完成了系列Post-Iboga 類型吲哚生物鹼的首次不對稱全合成工作。自 2021 年參加工作以來,一直從事Aspidosperma 類吲哚生物鹼的全合成研究工作,目前已完成了該家族 18 個複雜吲哚生物鹼的首次或更高效全合成。
學術論文
以第一作者(共同)和共同通訊作者身份發表的文章:
1. D.-X. Tan, J. Zhou, C.-Y. Gu, Z.-Y. Li, Y.-J. Shen, F.-S. Han*. Enantioselective Total Syntheses of Melotenine-, Voacafrine-, and Tabersonine-Type Aspidosperma Indole Alkaloids. Chem,2025, DOI: 10.1016/j.chempr.2025.102440. (IF = 19.1).
2. Y.-H. Zhang, L.-H. Deng, D.-X. Tan*, F.-S Han*. Catalytic Asymmetric Total Synthesis of (+)-Chamaecydin and (+)-Isochamaecydin and their Stereoisomers. Angew. Chem. Int. Ed.,2025, e202423944. (IF = 16.1).
3. D.-X. Tan#, J. Zhou#, C.-Y. Liu, F.-S. Han,* Enantioselective Total Synthesis and Configuration Assignment of (+)-Tronocarpine Enabled by an Asymmetric Michael/Aldol Reaction.Angew. Chem. Int. Ed., 2020, 59, 3834. (IF = 16.1). (Frontispiece Cover). (#: co-first authors)
4. J. Zhou#, D.-X. Tan#, F.-S. Han,* A Divergent Enantioselective Total Synthesis of Post-Iboga Indole Alkaloids. Angew. Chem. Int. Ed., 2020, 59, 18731. (IF = 16.1). (Highlight bySYNFACTS 2020, 16, 1012). (#: co-first authors).
5. G.-J. Wu#, D.-X. Tan#, F.-S. Han,* The Phosphinamide-Based Catalysts: Discovery,Methodology Development, and Applications in Natural Product Synthesis. Acc. Chem.Res., 2021, 54, 4354. (IF = 16.4). (#: co-first authors).
6. D.-X. Tan, J. Zhou, F.-S. Han,* An Updated Asymmetric Total Synthesis of (+)-Tronocarpine.Tetrahedron, 2020, 76, 131641. (IF = 2.1).
7. D.-X. Tan, F.-S. Han,* Synthetic Studies on Total Synthesis of Indole Alkaloids Containing Indolyl Lactam Frameworks. Synlett, 2021, 32, 663. (IF = 1.7).
8. D.-X. Tan, F.-S. Han,* The Application of C-H Bond Functionalization in the Total Syntheses of Indole Natural Products. Org. Chem. Front., 2022, 9, 1195. (IF = 4.6).
9. T. Liu, Y.-N. Chen, D.-X. Tan,* F.-S. Han,* The 2,4-Diarylquinoline-based Platinum (II) Complexs: Synthesis, Photophysical and Electrochemical Properties, and Application in Detection of Hypochlorite. J. Organomet. Chem., 2022, 977, 122453. (IF = 2.1).
10. C.-Y. Gu, J. Zhou, D.-X. Tan,* F.-S Han,* A Concise and Flexible Synthesis of C2’-Sulfonylated Quinine Derivatives. Synthesis, 2023, 55, 3991. (IF = 2.2).
11. Y. Zhao, G.-J. Wu, D.-X. Tan,* F.-S. Han,* Pd-catalyzed Room Temperature Hydrodeoxygenation of Aryl Sulfonates by Tuning the Stereoelectronic Nature of Ligands.Tetrahedron, 2024, 162, 134120. (IF = 2.1).
12. D.-X. Tan, Z.-J. Xu, H.-J. Chen, Y.-K. Wu,*Synthesis and Configurations of (–)-Furospongin-1 and (+)-Dihydrofurospongin-2. Eur. J. Org. Chem., 2016, 946. (IF = 2.5).
13. D.-X. Tan, Z.-J. Xu, M.-R. Xu, Y.-K. Wu,* J. You,* Several Enantiopure Chiral Building Blocks Derived from D-mannose. Chin. J. Chem., 2016, 34, 669. (IF = 5.5).
14. D.-X. Tan, J. You, M.-R. Xu, Y.-K. Wu,* Greatly Accelerated Condensation of D-mannose Diacetonide with Aqueous Formaldehyde (Formalin). J. Org. Chem., 2016, 81, 6792. (IF =3.3).
非第一作者及通訊作者的文章:
1. Z.-J. Xu, D.-X. Tan, Y.-K. Wu,* Synthesis and Structural Reassignment of Plakinidone. Org.Lett., 2015, 17, 5092. (IF = 4.9).
2. G.-J. Wu, Y.-H. Zhang, D.-X. Tan, F.-S. Han,* Total Synthesis of Cyrneines A, B, and Glaucopine C. Nat. Commun., 2018, 9, 2148. (Highlighted by SYNFACTS, 2018, 14, 0787). (IF= 14.7).
3. G.-J. Wu,# Y.-H. Zhang,# D.-X. Tan, L. He, B.-C. Cao, Y.-P. He, F.-S. Han,* Synthetic Studies on Enantioselective Total Synthesis of Cyathane Diterpenoids: Cyrneines A and B, Glaucopine C, and (+)-Allocyathin B2. J. Org. Chem., 2019, 84, 3223. (The top 20 most download articles in March and April, 2019). (IF = 3.3).
所獲榮譽
中國化學會第十一屆“天然產物全合成-青年學術研討會(2024)”,新銳報告。
中國化學會-第十屆“天然產物全合成-青年學術研討會(2023)”,優秀牆報獎。
榮獲2020年度博士研究生國家獎學金。
榮獲2019年度中科院長春應化所-中國科大首屆“化學•未來”研究生學術論壇-生命化學與生態材料分論壇學術報告 一等獎。