Prior to CUG

 

16. Photochemical Asymmetric Nickel‐Catalyzed Acyl Cross-Coupling, Angew. Chem. Int. Ed. 2019, 58, 16854.

E. Gandolfo, X. Tang, S. Raha Roy, P. Melchiorre*

 

15. Alkene 1,2-Difunctionalization by Radical Alkenyl Migration, Angew. Chem. Int. Ed. 2018, 57, 814 (ESI Highly Cited Paper).

X. Tang, A. Studer*

 

14. a-Perfluoroalkyl-b-alkynylation of alkenes via radical alkynyl migration, Chem. Sci. 2017, 8, 6888 (Highlighted in Synfacts 2017, 13, 1186.).

X. Tang, A. Studer*

 

13. Copper-catalyzed synthesis of tetrasubstituted allenes from quaternary ammonium salts and Grignard reagents, Asian J. Org. Chem. 2017, 6, 1209.

S. Ma*, Q. Liu, X. Tang, Y. Cai

 

12. Sodium-Ketyl Radical Anions by Reverse Pinacol Reaction and their Coupling with Iodoarenes, Org. Lett. 2016, 18, 4448.

X. Tang, A. Studer*

 

11. Identifying a Highly Active Copper Catalyst for KA2 Reaction of Aromatic Ketones, Chem. Eur. J. 2016, 22, 2266.

Y. Cai, X. Tang, S. Ma*

 

10. Indium(III) Triflate-Catalyzed Efficient Prins-Type Cyclization of b-Allenols and Aldehydes, Adv. Synth. Catal. 2016, 358, 4019.

Y. Han, X. Tang, J. Cheng, S. Ma*

 

9. Cadmium Iodide-Mediated Allenylation of Terminal Alkynes for the Synthesis of Methyl-substituted Allenes, Org. Lett. 2015, 17, 1176 (Highlighted in Synfacts 2015, 11, 525; ChemInform 2015, 46).

X. Tang, Y. Han, S. Ma*

 

8. CuBr2-Catalyzed Enantioselective Routes to Highly Functionalized or Naturally Occurring Allenes, Org. Chem. Front. 2015, 2, 688 (Highlighted in ChemInform 2015, 46).

X. Tang, X. Huang, T. Cao, Y. Han, X. Jiang, W. Lin, Y. Tang, J. Zhang, Q. Yu, C. Fu, S. Ma*

 

7. Zinc Diiodide-Promoted Synthesis of Trisubstituted Allenes From Propargylic Amines, Org. Chem. Front. 2015, 2, 470. 

J. Kuang, X. Tang, S. Ma*

 

6. Enantioselective Double Manipulation on Tetrahydro- isoquinolines with Terminal Alkynes and Aldehydes under Copper(I) Catalysis, Angew. Chem. Int. Ed. 2014, 53, 277.

W. Lin, …, X. Tang, S. Ma*

5. Cadmium Iodide-Mediated Allenylation of Terminal Alkynes with Ketones, Nat. Commun. 2013, 4, 2450.

X. Tang, C. Zhu, T. Cao, J. Kuang, W. Lin, S. Ni, S. Ma*

 

4. CuBr for KA2 Reaction: En Route to Propargylic Amines Bearig a Quaternary Carbon Center, Chem. Commun. 2013, 49, 8976-8978 (Highlighted in ChemInform 2014, 45).

X. Tang, J. Kuang, S. Ma*

 

3. Highly Selective FeCl3-Catalyzed Cyclization of β-Sulfon- amidoallenes or β-Allenols and Aldehydes, ACS Catal. 2013, 3, 663-666.

J. Cheng, X. Tang, S. Ma*

 

2. Bimetallic Enantioselective Approach to Axially Chiral Allenes, Org. Lett. 2013, 15, 2254.

R. Lü, …, X. Tang, S. Ma*

 

1. FeCl3-Catalyzed Cyclization of α-Sulfonamido-Allenes with Aldehydes—the Substituent Effect, Chem. Commun. 2012, 48, 12074-12076.

J. Cheng, X. Tang, Y. Yu, S. Ma*