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Records 1 to 13 of 13
| Authors | Title | Journal | Year | Vol. |
Issue | Pages |
| Han, C.; Kim, E. H.; Colby, D. A. | Cleavage of Carbon−Carbon Bonds through the Mild Release of Trifluoroacetate: Generation of alpha,alpha-Difluoroenolates for Aldol Reactions | J. Am. Chem. Soc. | 2011 | 133 | 5802-5805 | |
| Riofski, M. V.; John, J. P.; Zheng, M. M.; Kirshner, J.; Colby, D. A. | Exploiting the Facile Release of Trifluoroacetate for the alpha-Methylenation of the Sterically Hindered Carbonyl Groups on (+)-Sclareolide and (–)-Eburnamonine | J. Org. Chem. | 2011 | 76 | 3676–3683 | |
| Gunn, E. J.; Williams, J. T.; Huynh, D. T.; Iannotti, M. J.; Han, C.; Barrios, F. J.; Kendall, S.; Glackins, C. A.; Colby, D. A.; Kirshner, J. Leuk. | The Natural Products Parthenolide and Andrographolide Exhibit Anticancer Stem Cell Activity in Multiple Myeloma | Lymphoma | 2011 | 52 | 1085–1097 | |
| Woods, J. R.; Mo, H.; Bieberich, A. A.; Alavanja, T.; Colby, D. A. | Fluorinated Amino-Derivatives of the Sesquiterpene Lactone, Parthenolide, as 19F NMR Probes in Deuterium-Free Environments | J. Med. Chem. | 2011 | 54 | 7934–7941 | |
| John, J. P.; Colby, D. A. | Synthesis of alpha-Halo-alpha,alpha-Difluoromethyl Ketones by a Trifluoroacetate Release/Halogenation Protocol | J. Org. Chem. | 2011 | 76 | 9163–9168 | |
| Mo., H.; Balko, K. M.; Colby, D. A. | A Practical No-Deuterium NMR Method for the Rapid Determination of 1-Octanol/Water Partition Coefficients of Pharmaceutical Agents | Bioorg. Med. Chem. Lett. | 2010 | 20 | 6712–6715 | |
| Barrios, F. J.; Zhang, X.; Colby, D. A. | Dialkylaluminum N,O-Dimethylhydroxylamine Complex as a Reagent to Mask Reactive Carbonyl Groups in situ from Nucleophiles | Org. Lett. | 2010 | 12 | 5588-5591 | |
| Ishikawa, H.; Colby, D. A.; Seto, S.; Va, P.; Tam, A.; Kakei, H.; Rayl, T. J.; Hwang, I.; Boger, D. L. | Total Synthesis of Vinblastine, Vincristine, Related Natural Products, and Key Structural Analogues | J. Am. Chem. Soc. | 2009 | 131 | 4904-4916 | |
| Han, C.; Barrios, F. J.; Riofski, M. V.; Colby, D. A. | Semisynthetic Derivatives of Sesquiterpene Lactones by Palladium-Catalyzed Arylation of the alpha-Methylene-gamma-lactone Substructure. | J. Org. Chem. | 2009 | 74 | 7176-7179 | |
| Ishikawa, H.; Colby, D. A.; Boger, D. L. | Direct Coupling of Catharanthine and Vindoline to Provide Vinblastine: Total Synthesis of (+)- and ent-(-)- Vinblastine | J. Am. Chem. Soc. | 2008 | 130 | 420-421 | |
| Lawhorn, B. G.; Boga, S. B.; Wolkenberg, S. E.; Colby, D. A.; Guass, C. -M.; Swingle, M. R.; Amable, L.; Honkanen, R. E.; Boger, D. L. | Total Synthesis and Evaluation of Cytostatin, its C10-C11 Diastereomers, and Additional Key Analogues: Impact on PP2A Inhibition | J. Am. Chem. Soc. | 2006 | 128 | 16720-16732 | |
| Colby, D. A.; Liu, W.; Sheppeck, J. E.; Huang, H.-B.; Nairn, A. C.; Chamberlin A. R. | A New Model of the Tautomycin-PP1 Complex That Is Not Analogous to the Corresponding Okadaic Acid Structure | Bioorg. Med. Chem. Lett. | 2003 | 13 | 1601-1605 | |
| Liu, W.; Sheppeck, J. E.; Colby, D. A.; Huang, H.-B.; Nairn, A. C.; Chamberlin A. R. | The Selective Inhibition of Phosphatases by Natural Toxins: the Anhydride Domain of Tautomycin is Not a Primary Factor in Controlling PP1/PP2A Selectivity | Bioorg. Med. Chem. Lett. | 2003 | 13 | 1597-1600 |
