公開日期 | 題名 | 作者 | 關聯 | scopus | WOS | 全文 |
1990 | A New Nad-Dependent Alcohol-Dehydrogenase with Opposite Facial Selectivity Useful for Asymmetric Reduction and Cofactor Regeneration | Shen, G. J.; Wang, Y. F.; Bradshaw, C.; Wong, C. H. | JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS 677-679 | | | |
2003 | A new reactivity-based one-pot synthesis of N-acetyllactosamine oligomers | Mong, T. K.; Huang, C. Y.; Wong, C. H. | J Org Chem 68, 2135-2142 | | | |
1994 | A New Route to Deoxythiosugars Based on Aldolases | Chou, W. C.; Chen, L. H.; Fang, J. M.; Wong, C. H. | J Am Chem Soc 116, 6191-6194 | | | |
2005 | A new strategy for glycoprotein synthesis: ligation of synthetic glycopeptides with truncated proteins expressed in E. coli as TEV protease cleavable fusion protein | Tolbert, T. J.; Franke, D.; Wong, C. H. | Bioorganic & medicinal chemistry 13, 909-915 | | | |
1995 | A new strategy for the cloning, overexpression and one step purification of three DHAP-dependent aldolases: rhamnulose-1-phosphate aldolase, fuculose-1-phosphate aldolase and tagatose-1,6-diphosphate aldolase | Garcia Junceda, E.; Shen, G. J.; Sugai, T.; Wong, C. H. | BIOORGANIC & MEDICINAL CHEMISTRY 3, 945-953 | | | |
2004 | A new strategy for the synthesis of glycoproteins | Zhang, Z.; Gildersleeve, J.; Yang, Y. Y.; Xu, R.; Loo, J. A.; Uryu, S.; Wong, C. H.; Schultz, P. G. | Science 303, 371-373 | | | |
1992 | A New Strategy for the Synthesis of Nucleoside Analogs Based on Enzyme-Catalyzed Aldol Reactions | Liu, K. K. C.; Wong, C. H. | J Org Chem 57, 4789-4791 | | | |
2002 | A pH sensitive colorometric assay for the high-throughput screening of enzyme inhibitors and substrates: a case study using kinases | Chapman, E.; Wong, C. H. | BIOORGANIC & MEDICINAL CHEMISTRY 10, 551-555 | | | |
2003 | A potent and highly selective inhibitor of human alpha-1,3-fucosyltransferase via click chemistry | Lee, L. V.; Mitchell, M. L.; Huang, S. J.; Fokin, V. V.; Sharpless, K. B.; Wong, C. H. | J Am Chem Soc 125, 9588-9589 | | | |
2002 | A potent and highly selective sulfotransferase inhibitor | Chapman, E.; Ding, S.; Schultz, P. G.; Wong, C. H. | J Am Chem Soc 124, 14524-14525 | | | |
2003 | A programmable one-pot oligosaccharide synthesis for diversifying the sugar domains of natural products: a case study of vancomycin | Ritter, T. K.; Mong, K. K.; Liu, H.; Nakatani, T.; Wong, C. H. | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 42, 4657-4660 | | | |
1992 | A Pseudomonas Sp Alcohol-Dehydrogenase with Broad Substrate-Specificity and Unusual Stereospecificity for Organic-Synthesis | Bradshaw, C. W.; Fu, H.; Shen, G. J.; Wong, C. H. | J Org Chem 57, 1526-1532 | | | |
2002 | A quick diversity-oriented amide-forming reaction to optimize P-subsite residues of HIV protease inhibitors | Brik, A.; Lin, Y. C.; Elder, J.; Wong, C. H. | Chem Biol 9, 891-896 | | | |
1988 | A Search for Peptide Ligase - Cosolvent-Mediated Conversion of Proteases to Esterases for Irreversible Synthesis of Peptides | Barbas, C. F.; Matos, J. R.; West, J. B.; Wong, C. H. | J Am Chem Soc 110, 5162-5166 | | | |
1997 | A search for pyrophosphate mimics for the development of substrates and inhibitors of glycosyltransferases | Wang, R.; Steensma, D. H.; Takaoka, Y.; Yun, J. W.; Kajimoto, T.; Wong, C. H. | BIOORGANIC & MEDICINAL CHEMISTRY 5, 661-672 | | | |
1995 | A Short Enzymatic-Synthesis of L-Glucose from Dihydroxyacetone Phosphate and L-Glyceraldehyde | Alajarin, R.; Garciajunceda, E.; Wong, C. H. | J Org Chem 60, 4294-4295 | | | |
2002 | A strategy for the one-pot synthesis of sialylated oligosaccharides | Zhang, Z. Y.; Niikura, K.; Huang, X. F.; Wong, C. H. | CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE 80, 1051-1054 | | | |
2000 | A strategy for the solution-phase parallel synthesis of N-(pyrrolidinylmethyl)hydroxamic acids | Takayanagi, M.; Flessner, T.; Wong, C. H. | J Org Chem 65, 3811-3815 | | | |
1998 | A synthetic retrotransition (backward reading) sequence of the right-handed three-helix bundle domain (10-53) of protein A shows similarity in conformation as predicted by computation | Witte, K.; Skolnick, J.; Wong, C. H. | J Am Chem Soc 120, 13042-13045 | | | |
2004 | A three-fluorophore FRET assay for high-throughput screening of small-molecule inhibitors of ribosome assembly | Klostermeier, D.; Sears, P.; Wong, C. H.; Millar, D. P.; Williamson, J. R. | Nucleic Acids Res 32, 2707-2715 | | | |