- [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.