Xue-Wei Liu
Affiliations: | Nanyang Technological University, Singapore, Singapore |
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Parents
Sign in to add mentor| Charles E. McKenna | grad student | 2000 | USC |
| Linda C. Hsieh-Wilson | post-doc | 2003-2005 | Caltech |
Children
Sign in to add trainee| Seenuvasan Vedachala | grad student | 2008-2012 | Nanyang Technological University |
| Kumar Bhaskar Pal | post-doc | 2018-2021 | Nanyang Technological University |
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Publications
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| Zhang Y, Zhang XL, Ding H, et al. (2025) Streamlined Access to Peptidoglycan Biosynthesis Terminator GlcNAc-1,6-anhydro-MurNAc. Organic Letters |
| Zhao X, Ding H, Guo A, et al. (2024) Zinc(ii)-mediated stereoselective construction of 1,2- 2-azido-2-deoxy glycosidic linkage: assembly of K48 capsular pentasaccharide derivative. Chemical Science. 15: 12889-12899 |
| Zhang XL, Báti G, Li C, et al. (2024) GlcNAc-1,6-anhydro-MurNAc Moiety Affords Unusual Glycosyl Acceptor that Terminates Peptidoglycan Elongation. Journal of the American Chemical Society |
| Yip BRP, Pal KB, Lin JD, et al. (2021) Easy access to secondary and tertiary alcohols metal-free and light mediated radical carbonyl allylation. Chemical Communications (Cambridge, England) |
| Pal KB, Guo A, Das M, et al. (2020) Iridium-promoted deoxyglycoside synthesis: stereoselectivity and mechanistic insight. Chemical Science. 12: 2209-2216 |
| Pal KB, Lee J, Das M, et al. (2020) Palladium(ii)-catalyzed stereoselective synthesis of C-glycosides from glycals with diaryliodonium salts. Organic & Biomolecular Chemistry |
| Báti G, He JX, Pal KB, et al. (2019) Stereo- and regioselective glycosylation with protection-less sugar derivatives: an alluring strategy to access glycans and natural products. Chemical Society Reviews |
| Leng WL, Yao H, He JX, et al. (2018) Venturing beyond Donor-Controlled Glycosylation: New Perspectives toward Anomeric Selectivity. Accounts of Chemical Research |
| Huang N, Liao H, Yao H, et al. (2017) Diastereoselective Synthesis of C-Vinyl Glycosides via Gold(I)-Catalyzed Tandem 1,3-Acyloxy Migration/Ferrier Rearrangement. Organic Letters |
| Ding F, Leow ML, Ma J, et al. (2014) Collective synthesis of 4-hydroxy-2-pyridone alkaloids and their antiproliferation activities. Chemistry, An Asian Journal. 9: 2548-54 |