- [1] 16. E. Gandolfo, X. Tang, S. Raha Roy, P. Melchiorre*, Photochemical Asymmetric Nickel‐Catalyzed Acyl Cross-Coupling, Angew. Chem. Int. Ed. 2019, 58, 16854.
- [2] 15. X. Tang, A. Studer*, Alkene 1,2-Difunctionalization by Radical Alkenyl Migration, Angew. Chem. Int. Ed. 2018, 57, 814 (ESI Highly Cited Paper).
- [3] 13. S. Ma*, Q. Liu, X. Tang, Y. Cai, Copper-catalyzed synthesis of tetrasubstituted allenes from quaternary ammonium salts and Grignard reagents, Asian J. Org. Chem. 2017, 6, 1209.
- [4] 12. X. Tang, A. Studer*, Sodium-Ketyl Radical Anions by Reverse Pinacol Reaction and their Coupling with Iodoarenes, Org. Lett. 2016, 18, 4448.
- [5] 11. Y. Cai, X. Tang, S. Ma*, Identifying a Highly Active Copper Catalyst for KA2 Reaction of Aromatic Ketones, Chem. Eur. J. 2016, 22, 2266.
- [6] 10. Y. Han, X. Tang, J. Cheng, S. Ma*, Indium(III) Triflate-Catalyzed Efficient Prins-Type Cyclization of b-Allenols and Aldehydes, Adv. Synth. Catal. 2016, 358, 4019.
- [7] 9. X. Tang, Y. Han, S. Ma*, 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).
- [8] 14. X. Tang, A. Studer*, a-Perfluoroalkyl-b-alkynylation of alkenes via radical alkynyl migration, Chem. Sci. 2017, 8, 6888 (Highlighted in Synfacts 2017, 13, 1186.).
- [9] 8. X. Tang, X. Huang, T. Cao, Y. Han, X. Jiang, W. Lin, Y. Tang, J. Zhang, Q. Yu, C. Fu, S. Ma*, CuBr2-Catalyzed Enantioselective Routes to Highly Functionalized or Naturally Occurring Allenes, Org. Chem. Front. 2015, 2, 688 (Highlighted in ChemInform 2015, 46).
- [10] 7. J. Kuang, X. Tang, S. Ma*, Zinc Diiodide-Promoted Synthesis of Trisubstituted Allenes From Propargylic Amines, Org. Chem. Front. 2015, 2, 470.
- [11] 6. W. Lin, …, X. Tang, S. Ma*, Enantioselective Double Manipulation on Tetrahydro- isoquinolines with Terminal Alkynes and Aldehydes under Copper(I) Catalysis, Angew. Chem. Int. Ed. 2014, 53, 277.
- [12] 5. X. Tang, C. Zhu, T. Cao, J. Kuang, W. Lin, S. Ni, S. Ma*, Cadmium Iodide-Mediated Allenylation of Terminal Alkynes with Ketones, Nat. Commun. 2013, 4, 2450.
- [13] 4. X. Tang, J. Kuang, S. Ma*, 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).
- [14] 3. J. Cheng, X. Tang, S. Ma*, Highly Selective FeCl3-Catalyzed Cyclization of β-Sulfon- amidoallenes or β-Allenols and Aldehydes, ACS Catal. 2013, 3, 663-666.
- [15] 2. R. Lü, …, X. Tang, S. Ma*, Bimetallic Enantioselective Approach to Axially Chiral Allenes, Org. Lett. 2013, 15, 2254.
- [16] 1. J. Cheng, X. Tang, Y. Yu, S. Ma*, FeCl3-Catalyzed Cyclization of α-Sulfonamido-Allenes with Aldehydes—the Substituent Effect, Chem. Commun. 2012, 48, 12074-12076.
| |