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成果及论文

2024

8. Pei-Hao Dou, Xiao-Hui Fu, Yan Chen, Zhen-Zhen Ge, Ming-Qiang Zhou, Zhen-Hua Wang, Yong You, Lei Yang, Yan-Ping Zhang, Jian-Qiang Zhao*, and Wei-Cheng Yuan* Palladium-Catalyzed Asymmetric Decarboxylation of 5-Vinyloxazolidine-2,4-Diones Triggering the Dearomatization of Electron-Deficient Indoles for the Synthesis of Chiral Highly Functionalized Pyrroloindolines. Organic Letters, Articles ASAP DOI:https://doi.org/10.1021/acs.orglett.4c01003

Abstract Image

7. Jun-Rui Zhuo, Jian-Qiang Zhao*, Lei Yang, Yu-Lu Wu, Yan-Ping Zhang, Yong You, Zhen-Hua Wang, Ming-Qiang Zhou, and Wei-Cheng Yuan* Thiol-Triggered Tandem Dearomative Michael Addition/Intramolecular Henry Reaction of 2-Nitrobenzofurans: Access to Sulfur-Containing Polyheterocyclic Compounds. Org. Lett. 2024, DOI:10.1021/acs.orglett.4c0064

6. Xiaohui Fu , Yanping Zhang , Juan Liao , Zhen-Hua Wang ,Yong You , Jian-Qiang Zhao , Mingqiang Zhou , Wei-Cheng Yuan* Palladium-catalyzed enantioselective decarboxylation of vinyl cyclic carbamates: generation of amide-based aza-1,3-dipoles and application to asymmetric 1,3-dipolar cycloaddition. Chinese Chemical Letter (2024) https://doi.org/10.1016/j.cclet.2024.109688

Image, graphical abstract

5. Cu-Catalyzed Direct Asymmetric Mannich Reaction of 2-Alkylazaarenes and Isatin-Derived Ketimines. Yao-Bin Shen, Hui-Ling Qian, Lei Yang, Shun Zhou, Han-Wen Rao, Zhen-Hua Wang, Yong You, Yan-Ping Zhang, Jun-Qing Yin, Jian-Qiang Zhao*, Wenjing Zhang*, and Wei-Cheng Yuan*. Org. Lett. 2024, 26, 8, 1699–1704

Abstract Image

4. Zhen-Hua Wang*, Xiao-Hui Fu, Qun Li, Jian-Qiang Zhao, Yong You, Yan-Ping Zhang, and Wei-Cheng Yuan*. Palladium-Catalyzed Ligand-Directed Divergent Decarboxylative Cycloadditions of Vinyloxazolidine-2,4-diones with 1,3,5-Triazinanes. Org. Lett., 2024, 26, 1589-1594.

3. Tong Zhang, Zhen-Hua Wang*, Yong Li, Jian-Qiang Zhao, Yong You, Yan-Ping Zhang, Jun-Qing Yin and Wei-Cheng Yuan*, Chiral phosphoric acid-catalyzed enantioselective synthesis of functionalized pyrrolinones containing a geminal diamine core via an aza-Friedel–Crafts reaction of newly developed pyrrolinone ketimines. Org. Chem. Front., 2024, 11, 1437-1443.


2. Wei-Cheng Yuan*, Hai-Ying Zeng , Yan-Ping Zhang , Jian-Qiang Zhao, Yong You, Jun-Qing Yin, Ming-Qiang Zhou,* and Zhen-Hua Wang.* Synthesis of Benzofuro[3,2-b]indol-3-one Derivatives via Dearomative (3 + 2) Cycloaddition of 2-Nitrobenzofurans and para-Quinamines. Molecules 2024, 29(5), 1163.


1. Yong You, Guo-Ying Gan, Qun Li, Xiong-Li Liu, Yan-Ping Zhang, Zhen-Hua Wang, Jian-Qiang Zhao and Wei-Cheng Yuan Enantioselective [3 + 2] annulation of tryptanthrin-derived ketimines and 2-naphthols: access to polycyclic indolo[2,1-b]quinazoline derivatives. Org. Chem. Front., 2024,11, 2002-2007

Graphical abstract: Enantioselective [3 + 2] annulation of tryptanthrin-derived ketimines and 2-naphthols: access to polycyclic indolo[2,1-b]quinazoline derivatives


2023年以前成果

2023

Org.   Biomol. Chem., 2023, 21, 1373-1378

2022

Chem. Commun., 2022, 58, 553–556

Chem. Commun., 2023, 59, 7483-7505

Org. Chem. Front., 2022, 9, 88–94

Org. Biomol. Chem., 2023, 21,   8593-8602

Tetrahedron 116 (2022) 132810

Org. Chem. Front., 2023, 10, 3130-3168

ChemCatChem 2022, 14, e202101887

Org. Chem. Front., 2023, 10, 4256-4262

Chirality, 2022,34,1019-1034

Org. Chem. Front., 2023, 10, 5421-5427

Chem. Commun., 2022, 58, 12062-12065

Org. Chem. Front., 2023, 10, 5971-5977

Org. Biomol. Chem., 2022, 20,   5060-5065

Eur. J. Org. Chem.,2023,26,  e202300728

Org. Chem. Front., 2022, 9, 3322-3327

Molecules   2023, 28, 2765

Org. Chem. Front., 2022, 9, 6172-6178

Molecules   2023, 28, 3059

J. Org. Chem.2022, 87, 6025-6037

Molecules   2023, 28, 4410

Eur. J. Org. Chem.,2022, e202200110

Molecules   2023, 28, 5372

Org.Lett., 2022, 24, 5120-5125

Molecules   2023, 28, 5529

J. Org. Chem.2022, 87, 4232-4240

Molecules   2023, 28, 7898

Org.Lett., 2022, 24, 1094-1099

Org.Lett., 2023, 25, 9191-9196

J. Org. Chem.2022, 87, 5804-5816

Org.Lett., 2023, 25, 1274-1279

Org.Lett., 2022, 24, 4052-4057

Org.Lett., 2023, 25, 8027-8032

Org.Lett., 2022, 24, 7671-7676

 

Org.Lett., 2022, 24, 826-831

Org.Lett., 2022, 24, 8348-8353

Org.Lett., 2022, 24, 4603-4608

2021

Adv. Synth.Catal.2021,363,  1702–1713

2020

Chem. Commun., 2020, 56, 439--442

Adv. Synth.Catal.2021,363,  4047–4053

Chem. Commun., 2020, 56, 2586--2589

Chem. Commun., 2021, 57, 2927-2930

Chem. Commun., 2020, 56, 12363--12366

Chem. Commun., 2021, 57, 4938–4941

Chem. Commun., 2020, 56, 13449--13452

J. Org. Chem. 2021, 86, 1779−1788

J. Org. Chem.2020, 85, 11812−11821

J. Org. Chem.2021, 86, 2534−2544

Org. Biomol. Chem., 2020, 18, 845–850

J. Org. Chem.2021, 86, 6711−6720

Org. Biomol. Chem., 2020, 18,   1886–1891

J. Org. Chem.2021, 86, 11472−11481

Org. Biomol. Chem., 2020, 18,   4560–4565

Org. Biomol. Chem., 2021, 19,   3678–3686

Org. Chem. Front., 2020, 7, 499–506

Org. Chem. Front., 2021, 8, 784–791

Org.Lett.2020, 22, 3114−3118

Org. Chem. Front., 2021, 8, 6330–6336

Org.Lett.2020, 22, 7088−7093

Org.Lett.2021, 23, 8600−8605

Tetrahedron 76 (2020) 131115

Tetrahedron Letters 67 (2021) 152862

Tetrahedron 76 (2020) 131116

2019

Chem. Commun., 2019, 55, 8478--8481

 

Chem. Commun., 2019, 55, 9327--9330

ChemistrySelect2019,4,  4156– 4158

ChemistrySelect2019,4, 4458–4461

Eur.   J. Org. Chem.2019, 3112–3116

J. Org. Chem.2019, 84, 4381−4391

J. Org. Chem.2019, 84, 7984−7994

Org. Biomol. Chem., 2019, 17,   5294–5304

Org. Biomol. Chem., 2019, 17,   6551–6556

Org. Chem. Front., 2019, 6, 1879–1884

Org. Chem. Front., 2019, 6, 3342–3347

Org.Lett.2019, 21, 660−664

Org.Lett.2019, 21, 5452−5456

Synlett 2019, 30, A–F

Synthesis 2019, 51, A–L

Tetrahedron 75 (2019) 2155-2161

Tetrahedron 75 (2019) 2206-2214

Tetrahedron 75 (2019) 3456e3462

Tetrahedron 75 (2019) 130571