The Xu Group at CCNU

22

Wei-Feng Qian,# Yan-Yan Ouyang,# Cuiju‍‍‍‍‍ ‍Zhu,* Hao Xu*   ‍

Electrochemical Cascade Cyclization of N-Centered Radicalswith Electro-DeficientAlkynes.

ChemCatChem. 10.1002/cctc.202301572‍.

(Invited contribution to Special Collection "ChineseCatChem").

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20

Ying Li (本科生),
Kongling Feng (本科生)
,
Ruinan Zhao
,
Cuiju Zhu
,
Hao Xu

Dearomatization of α-Unsubstituted β-Naphthols.

Synlett.2023, 14, 70469.

(Special Issue Thieme Chemistry Journals Awardees 2023)



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19

Zi-Qi Geng,# Chunhui Zhao (本科生),# Hao-Dong Qian, Si-Jia Li, Hao Peng*, and Hao Xu*
Cu/Ag-Mediated One-Pot Enantioselective Synthesis of FullyDecorated 1,2,3-Triazolo[1,5‑a]pyrazines

Org.Lett.2023,25, 45044509.


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14
Hao-Dong Qian§, Zhi-Heng Li§, Shuang Deng, Chaochao Yao, Hua-Ming Xiang, Guang Xu, Zi-Qi Geng, Zihao Wang, Linfeng Chen, Chunrong Liu, Cuiju Zhu, Xiaotian Qi, and Hao Xu*

(Highlighted by Synfacts 2022, 18, 1204.; Highlighted by X-MOL)

12

Zhi-Heng Li§, Dan-Ran Li§, Hua-Ming Xiang, Jian Huang, Yi-Nuo Zheng(本科生), Cuiju Zhu, Xiuling Cui, Chao Pi*, and Hao Xu*

Copper-Catalyzed Asymmetric Propargylic Substitution of Anthrones and Propargylic Esters

Chinese Chem. Lett. 2022, 33 , 867–870.

11

Jian Huang§, Han-Han Kong§, Si-Jia Li, Rui-Jin Zhang, Hao-Dong Qian, Dan-Ran Li(本科生), Jin-Yu He, Yi-Nuo Zheng(本科生), and Hao Xu*

Asymmetric Copper–Catalyzed Propargylic Amination with Amine Hydrochloride Salts.

Chem. Comm. 2021, 57, 46744677. (This article is part of the themed collection: 2021 Emerging Investigators)

10

Julian Wilke, Tatsuro Kawamura, Hao Xu, Alexandra Brause, Alexandra Friese, Malte Metz, Dirk Schepmann, Bernhard Wünsch, Antonia Artacho-Cordón, Francisco R.Nieto, Nobumoto Watanabe, Hiroyuki Osada, Slava Ziegler, Herbert Waldmann*

Discovery of a σ1 receptor antagonist by combination of unbiased cell painting and thermal proteome profiling.

Cell Chem. Biol. 2021, 28, 848–854.

9

Si-Jia Li§, Jian Huang§, Jin-Yu He, Rui-Jin Zhang, Hao-Dong Qian, Xue-Lin Dai (本科生), Han-Han Kong and Hao Xu*

Highly enantioselective copper-catalyzed propargylic amination to access N-tethered 1,6-enynes.

RSC Adv. 2020, 10, 38478.

 A highly enantioselective copper-catalyzed propargylic amination starting from benzylic allylic amines has been developed with a new chiral N,N,P ligand, providing a series of N-tethered 1,6-enynes in good to excellent yields with excellent enantioselectivities.

8

Hao Xu, Luca Laraia, Laura Schneider, Kathrin Louven, Carsten Strohmann, Andrey P. Antonchick* and Herbert Waldmann*;

Highly Enantioselective Catalytic Vinylogous Propargylation of Coumarins Yields a Class of Autophagy Inhibitors.

Angew. Chem. Int. Ed. 2017, 56, 11232.

(Highlighted by Synfacts. 2017, 13, 1047.)

7

Hao Xu, Christopher Golz, Carsten Strohmann, Andrey P. Antonchick* and Herbert Waldmann*;

Enantiodivergent Combination of Natural Product Scaffolds Enabled by Catalytic Enantioselective Cycloaddition.

Angew. Chem. Int. Ed. 2016, 55, 7761.

6

Hao Xu§, Jiang-Lin Hu§, Li-Jia Wang, Sai-Hu Liao and Yong Tang*;

Asymmetric Annulation of Donor−Acceptor Cyclopropanes with Dienes. (§: contributed equally)

J. Am. Chem. Soc. 2015, 137, 8006.

(Highlighted by Synfacts. 2015, 11, 956.)

5

Jiang-Lin Hu, Li-Jia Wang, Hao Xu, Zuo-Wei Xie* and Yong Tang*;

Highly Diastereoselective and Enantioselective Formal [4 + 3] Cycloaddition of Donor–Acceptor Cyclobutanes with Nitrones.

Org. Lett. 2015, 17, 2680.

4

Hao Xu§, Jian-Ping Qu§, Sai-Hu Liao, Hu Xiong and Yong Tang*;

Highly Enantioselective [3+2] Annulation of Cyclic Enol Silyl Ethers with Donor–Acceptor Cyclopropanes: Accessing 3a-Hydroxy [n.3.0]Carbobicycles. ( §: contributed equally)

Angew. Chem. Int. Ed. 2013, 52, 4004. (Selected as a Hot paper)

(Highlighted by Synfacts. 2013, 9, 648.)

3

Hu Xiong§, Hao Xu§, Sai-Hu Liao, Zuo-Wei Xie* and Yong Tang*;

Copper-Catalyzed Highly Enantioselective Cyclopentannulation of Indoles with Donor−Acceptor Cyclopropanes.

( §: contributed equally)

J.
Am. Chem. Soc.
2013, 135, 7851.

(Highlighted by Synform, 2013, 7, 122.)

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