At NWU:
27. Zhu, D.* Chemical Synthesis 2024-2025, In Preparation. (Invited article)
26. Zhu, D.* Org. Biomol. Chem., 2024-2025, In Preparation. (Invited article)
25. Zhu, D.* Chem. Commun., 2024, In Preparation. (Invited article)
24. Yang, L.†; Yu, L.†; Liu, L.; Wang, L.; Zhong, Y.; Liang, F.; Zheng, C.; Liu, J.-Q.; Xue, X.-S.*; Zhu, D.* 2024, In Submission.
23. Liu, L.†; Hou J.†; Ma, Y.; Xu, W.-H.; Liu, J.-Q.; Zhu, D.* Collaborative Reduction-Induced Nickel-Catalytic Selective C-S Coupling of Aryl Di/Trithiosulfonates with Aryl Halides. Org. Lett. 2024, DOI: 10.1021/acs.orglett.4c04390. (IF: 4.9, Q1)
22. Liang, F.; Zhu, D.* Trifluoromethylsulfinyl Compounds: Recent Synthetic Approaches and Future Perspectives. Eur. J. Org. Chem., 2024, DOI: 10.1002/ejoc.202400569. (IF: 2.8, Q3) (Invited review, highlighted by WileyChem)
This paper is collected as special issue of "Fluorine Chemistry: New Trends".
This paper is dedicated to Professor Long Lu (SIOC) on the occasion of his 60th birthday.
21. Shan, D.†; Jiang, M.†; Liang, F.; Zhong, Y.; Zhu, D.* Direct Dehydroxy(sulfhydryl)xanthylation of Alcohols and Thiols. Org. Chem. Front., 2024, 11, 3675-3684. (IF: 5.4, Q1) (Highlighted by Frontiers Jornals and CBG)
20. Liu, L.†; Hou J.†; Ma, Y.; Wang, H. (西北大学2022级本科生); Zhong, Y.; Liang, F.; Wang, L.; Wang, Q.*; Liu, J.-Q.; Xu, W.-H.; Zhu, D.* Selective Nickel-Catalyzed Disulfuration of Alkyl Halides with Di/Trithiosulfonates. Org. Chem. Front., 2024, 11, 3196-3203. (IF: 5.4, Q1) (Highlighted by Frontiers Jornals)
19. Li, Y.; Liu, L.; Shan, D.; Liang, F.; Wang, S.; Yu, L.; Liu, J.-Q.; Wang, Q.*; Shao, X.*; Zhu, D.* Exploration on Metal-Catalytic Conversion of Sulfinyl Sulfones. ACS Catal., 2023, 13, 13474−13483. (IF: 12.9, Q1 Top) (Highlighted by X-mol, CBG, 研之成理, 岳麓化学)
This paper is dedicated to Professor Chao-Jun Li (McGill University) on the occasion of his 60th birthday.
18. Wang, S.†; Yang, L.†; Liang, F.; Zhong, Y.; Liu, X.; Wang, Q.*; Zhu, D.* Synthetic Exploration of Electrophilic Xanthylation via Powerful N-Xanthylphthalimides. Chem. Sci., 2023, 14, 9197-9206. (IF: 8.4, Q1 Top) (Highlighted by InfoMat and CBG)
17. Yang, L.†; Wang, S.†; Liang, F.#; Han, Y.; Li, Y.; Shan, D.; Liu, L.; Wang, Q.*; Zhu, D.* Direct Transfer Strategy of Trifluoromethylsulfinyl Group by a General Reagent N-Trifluoromethylsulfinylphthalimide under Catalytic or Stoichiometric Lewis Acid or Lewis Base. Org. Chem. Front., 2023, 10, 4368-4380. (IF: 5.4, Q1) (Highlighted by CBG)
16. Xing, S.; Ma, C.; Liu, W.; Ni, S.-F.*; Zhu, D.*; Xu, L.-W.; Shao, X.* Lewis Base-Catalyzed Trifluoromethylsulfinylation of Allylic Alcohols: Stability-Oriented Divergent Synthesis. Org. Lett., 2023, 25, 1066-1071. (IF: 5.2, Q1)
15. Yang, B.; Xue, W.; Yu, B.; Pang, H.; Yu, L.; Wang, Q.*; Zhu, D.* Development of Trimethylamine-Catalyzed Novel Synthesis of Azoxystrobin. Org. Process Res. Dev., 2023, 27, 1276-1282. (IF: 3.4, Q2) (农药嘧菌酯的合成工艺研究，highlighted by 化学深耕堂)
14. Wang, F.†; Han, Y.†; Yu, L.; Zhu, D.* Decarboxylative Amination of Benzoic Acids Bearing Electron-Donating Substituents and Non-Activated Amines. Org. Chem. Front., 2022, 9, 3281-3292. (IF: 5.4, Q1) (Highlighted by Frontiers Journals, CBG)
13. Tan, B.†; Liu, L.†; Zheng, H.; Cheng, T.; Zhu, D.*; Yang, X.; Luan, X.* Two-in-One Strategy for Fluorene-Based Spirocycles via Pd(0)-Catalyzed Spiroannulation of o-Iodobiaryls with Bromonaphthols. Chem. Sci., 2020, 11, 10198-10203. (IF: 9.6, Q1 Top)
Before NWU:
12. Li, C.-J.*; Huang, J.; Dai, X.-J.; Wang, H.; Chen, N.; Wei, W.; Zeng, H.; Tang, J.; Li, C.; Zhu, D.; Lv, L. An Old Dog with New Tricks: Enjoin Wolff–Kishner Reduction for Alcohol Deoxygenation and C–C Bond Formations. Synlett. 2019, 30, 1508-1524. (Review) (IF: 1.9, Q4)
11. Lv, L.; Zhu, D.; Qiu, Z.; Li, J.; Li, C. -J.* Nickel-Catalyzed Regioselective Hydrobenzylation of 1,3-Dienes with Hydrazones. ACS Catal., 2019, 9, 9199-9205. (IF: 12.9, Q1 Top)
10. Zhu, D.†; Lv, L.†; Qiu, Z.; Li, C. -J.* Nickel-catalyzed Cross-Coupling of Umpolung Carbonyls and Alkyl Halides. J. Org. Chem. 2019, 84, 6312-6322. (IF: 3.6, Q2) (Highlighted by Angew. Chem. Int. Ed. 2021, 60, 21624–21634; Chem. Soc. Rev., 2021,50, 10733-10742)
9. Lv, L.†; Zhu, D.†; Li, C. -J.* Direct Dehydrogenative Alkyl Heck-Couplings of Vinylarenes with Umpolung Aldehydes Catalyzed by Nickel. Nat. Commun. 2019, 10, 715. doi: 10.1038/s41467-019-08631-1. (IF: 16.2, Q1 Top) (Highlighted by Angew. Chem. Int. Ed. 2021, 60, 21624–21634; Chem. Soc. Rev., 2021,50, 10733-10742)
8. Zhu, D.†; Lv, L.†; Li, C. -C.; Ung, S.; Gao, J.; Li, C. -J.* Umpolung Carbonyl Groups as Alkyl Organometallic Reagent Surrogates for Palladium Catalyzed Allylic Alkylation. Angew. Chem. Int. Ed. 2018, 57, 16520-16524. (IF: 16.2, Q1 Top) (Highlighted by Angew. Chem. Int. Ed. 2021, 60, 21624–21634; Chem. Soc. Rev., 2021,50, 10733-10742)
7. Li, C. -C.; Dai, X. -J.; Wang, H.; Zhu, D.; Gao, J.; Li, C. -J.* Iron-Catalyzed Nucleophilic Addition Reaction of Organic Carbanion Equivalents via Hydrazones. Org. Lett., 2018, 20, 3801-3805. (IF: 5.2, Q1)
6. Li, J.†; Zhu, D.†; Lv, L.; Li, C. -J.* Radical Difluoromethylthiolation of Aromatics Enabled by Visible Light. Chem. Sci., 2018, 9, 5781-5786. (IF: 9.6, Q1 Top) (Editor's choice-Paolo Melchiorre; highlighted by X-mol)
5. Lv, L.†; Zhu, D.†; Tang, J.; Qiu, Z.; Li, C. -C.; Gao, J.; Li, C. -J.* Cross-Coupling of Phenol Derivatives with Umpolung Aldehydes Catalyzed by Nickel. ACS Catal., 2018, 8, 4622-4627. (IF: 12.9, Q1 Top) (Highlighted by Angew. Chem. Int. Ed. 2021, 60, 21624–21634; Chem. Soc. Rev., 2021,50, 10733-10742)
4. Zhu, D.; Hong, X.; Li, D.; Lu, L.; Shen, Q. A Two-Step, One-Pot, and Multigram-Scale Synthesis of N-Difluoromethylthio-phthalimide. Org. Process Res. Dev., 2017, 21, 1383-1387. (IF: 3.4, Q2)
3. Zhu, D.†; Shao, X.†; Hong, X.; Lu, L.*; Shen, Q.* PhSO2SCF2H: A Shelf-Stable, Easily Scalable Reagent for Radical Difluoromethylthiolation. Angew. Chem. Int. Ed. 2016, 55, 15807-15811. (IF: 16.2, Q1 Top) (Highlight by Acc. Chem. Res. 2021, 54, 2946-2958)
2. Zhu, D.†; Gu, Y.†; Lu, L.*; Shen, Q.* N-Difluoromethylthiophthalimide: A Shelf-Stable, Electrophilic Reagent for Difluoromethylthiolation. J. Am. Chem. Soc. 2015, 137, 10547-10553. (IF: 15.0, Q1 Top) (Highlighted by Chem.& Eng. News, 2015, 93, 45 and Acc. Chem. Res. 2021, 54, 2946-2958)
1. Hu, H.†; Shao, X.†; Zhu, D.; Lu, L.*; Shen, Q.* Silver-Catalyzed Decarboxylative Trifluoromethylthiolation of Aliphatic Carboxylic Acids in Aqueous Emulsion. Angew. Chem. Int. Ed. 2014, 53, 6105-6109. (IF: 16.2, Q1 Top)
(† 共同第一作者; * 通讯作者)