| New chiral phosphorus ligands for enantioselective hydrogenation W Tang, X Zhang Chemical Reviews 103 (8), 3029-3070, 2003 | 2695 | 2003 |
| A chiral 1, 2‐bisphospholane ligand with a novel structural motif: applications in highly enantioselective Rh‐catalyzed hydrogenations W Tang, X Zhang Angewandte Chemie 114 (9), 1682-1684, 2002 | 339 | 2002 |
| Efficient syntheses of korupensamines A, B and michellamine B by asymmetric Suzuki-Miyaura coupling reactions G Xu, W Fu, G Liu, CH Senanayake, W Tang Journal of the American Chemical Society 136 (2), 570-573, 2014 | 286 | 2014 |
| Highly Effective Chiral Ortho-Substituted BINAPO Ligands (o-BINAPO): Applications in Ru-Catalyzed Asymmetric Hydrogenations of β-Aryl-Substituted β … YG Zhou, W Tang, WB Wang, W Li, X Zhang Journal of the American Chemical Society 124 (18), 4952-4953, 2002 | 264 | 2002 |
| P-Chiral Phosphorus Ligands Based on a 2,3-Dihydrobenzo[d][1,3]oxaphosphole Motif for Asymmetric Catalysis G Xu, CH Senanayake, W Tang Accounts of chemical research 52 (4), 1101-1112, 2019 | 228 | 2019 |
| A general and special catalyst for Suzuki–Miyaura coupling processes W Tang, AG Capacci, X Wei, W Li, A White, ND Patel, J Savoie, JJ Gao, ... Angewandte Chemie 122 (34), 6015-6019, 2010 | 228 | 2010 |
| Chiral monophosphorus ligands for asymmetric catalytic reactions W Fu, W Tang ACS Catalysis 6 (8), 4814-4858, 2016 | 211 | 2016 |
| Enantioselective hydrogenation of tetrasubstituted olefins of cyclic β-(acylamino) acrylates W Tang, S Wu, X Zhang Journal of the American Chemical Society 125 (32), 9570-9571, 2003 | 198 | 2003 |
| A bisphosphepine ligand with stereogenic phosphorus centers for the practical synthesis of β‐aryl‐β‐amino acids by asymmetric hydrogenation W Tang, W Wang, Y Chi, X Zhang Angewandte Chemie 115 (30), 3633-3635, 2003 | 195 | 2003 |
| Highly efficient synthesis of chiral β-amino acid derivatives via asymmetric hydrogenation W Tang, X Zhang Organic letters 4 (23), 4159-4161, 2002 | 178 | 2002 |
| Synthesis of chiral α-amino tertiary boronic esters by enantioselective hydroboration of α-arylenamides N Hu, G Zhao, Y Zhang, X Liu, G Li, W Tang Journal of the American Chemical Society 137 (21), 6746-6749, 2015 | 176 | 2015 |
| Novel, tunable, and efficient chiral bisdihydrobenzooxaphosphole ligands for asymmetric hydrogenation W Tang, B Qu, AG Capacci, S Rodriguez, X Wei, N Haddad, B Narayanan, ... Organic Letters 12 (1), 176-179, 2010 | 169 | 2010 |
| Efficient chiral monophosphorus ligands for asymmetric Suzuki–Miyaura coupling reactions W Tang, ND Patel, G Xu, X Xu, J Savoie, S Ma, MH Hao, S Keshipeddy, ... Organic letters 14 (9), 2258-2261, 2012 | 167 | 2012 |
| Structural revision and total synthesis of azaspiracid‐1, part 2: Definition of the ABCD domain and total synthesis KC Nicolaou, TV Koftis, S Vyskocil, G Petrovic, T Ling, YMA Yamada, ... Angewandte Chemie 116 (33), 4418-4424, 2004 | 156 | 2004 |
| Phospholane—Oxazoline Ligands for Ir‐Catalyzed Asymmetric Hydrogenation. W Tang, W Wang, X Zhang ChemInform 34 (25), no-no, 2003 | 156 | 2003 |
| Enantioselective Palladium‐Catalyzed Dearomative Cyclization for the Efficient Synthesis of Terpenes and Steroids K Du, P Guo, Y Chen, Z Cao, Z Wang, W Tang Angewandte Chemie International Edition 54 (10), 3033-3037, 2015 | 154 | 2015 |
| Enantioselective formation of quaternary carbon stereocenters in natural product synthesis: a recent update C Li, SS Ragab, G Liu, W Tang Natural Product Reports 37 (2), 276-292, 2020 | 150 | 2020 |
| Asymmetric hydrogenation of itaconic acid and enol acetate derivatives with the Rh-tangPhos catalyst W Tang, D Liu, X Zhang Organic Letters 5 (2), 205-207, 2003 | 145 | 2003 |
| Design of Phosphorus Ligands with Deep Chiral Pockets: Practical Synthesis of Chiral β‐Arylamines by Asymmetric Hydrogenation G Liu, X Liu, Z Cai, G Jiao, G Xu, W Tang Angewandte Chemie International Edition 52 (15), 4235-4238, 2013 | 141 | 2013 |
| Copper catalyzed asymmetric propargylation of aldehydes DR Fandrick, KR Fandrick, JT Reeves, Z Tan, W Tang, AG Capacci, ... Journal of the American Chemical Society 132 (22), 7600-7601, 2010 | 140 | 2010 |
